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Progress in rehabilitation medicine · 2026

Применение периферального магнитного стимула в процессе реабилитации: обзор.

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Fukushima T, Hase K, Nakano J

Аннотация

Перпериферийная магнитная стимуляция все чаще используется для лечения дисфункций, связанных с различными расстройствами. Однако в настоящее время отсутствует консенсус в отношении его эффективности применительно к конкретным группам населения, болезням, условиям вмешательства, продолжительности лечения или результатам. Цель этого аналитического обзора заключалась в выявлении, обобщении и составлении карт соответствующей литературы по периферической магнитной стимуляции с уточнением ее применения в разбивке по типам заболеваний, участку лечения, функциональным дефектам, результатам и условиям вмешательства. Систематический поиск по методу A проводился в нескольких базах данных, включая PubMed/MEDLINE, CINAHL Complementary, Cochrane Bibrary, Web of Science и PEDro. Были проведены исследования по изучению воздействия периферической магнитной стимуляции на дисфункцию всех типов заболеваний и популяций. 804 - выверенные статьи, 97 отвечает критериям включения. Периферальная магнитная стимуляция использовалась главным образом для лечения заболеваний мускулоскелета, неврологических заболеваний и заболеваний, связанных с недержанием, с уделением особого внимания конкретным результатам, связанным с мышечными и физическими функциями в затронутых районах. С другой стороны, его применение во внутренних болезнях в основном ограничивалось хроническими обструктивными легочными заболеваниями, при этом лишь немногие исследования касались его эффективности в сердечно - сосудистых заболеваниях, раке и сахарном диабете. Кроме того, периферийные параметры магнитной стимуляции сильно варьировались, даже когда они применялись к аналогичным заболеваниям или дисфункциям. Однако его применение к внутренним болезням остается ограниченным, особенно к сердечно - сосудистым заболеваниям, раку и сахарному диабету. Кроме того, до сих пор не разработаны стандартизированные предписания в отношении периферийной магнитной стимуляции. В будущих исследованиях следует уделять особое внимание его применению в отношении недостаточно обслуживаемых заболеваний и дисфункций и разработать стандартные протоколы лечения.
Оригинал публикации

Applications of Peripheral Magnetic Stimulation in Rehabilitation: A Scoping Review.

BackgroundPeripheral magnetic stimulation is increasingly used to treat dysfunctions associated with various disorders. However, there is currently no consensus regarding its efficacy across specific populations, disease conditions, intervention settings, treatment durations, or outcomes. This scoping review aimed to identify, summarize, and map relevant literature on peripheral magnetic stimulation, clarifying its application by disease type, treatment site, functional impairments, outcomes, and intervention setting.MethodsA systematic search was conducted across several databases, including PubMed/MEDLINE, CINAHL Complete, Cochrane Library, Web of Science, and PEDro. Studies that examined the impact of peripheral magnetic stimulation on dysfunction across all disease types and populations were included.ResultsOf 804 screened articles, 97 met the inclusion criteria. Peripheral magnetic stimulation was primarily used for musculoskeletal, neurological, and incontinence-related diseases, focusing on disease-specific outcomes related to muscle and physical function in the affected areas. Conversely, its use in internal diseases was predominantly limited to chronic obstructive pulmonary disease, with few studies addressing its efficacy in cardiovascular diseases, cancer, and diabetes mellitus. Furthermore, peripheral magnetic stimulation settings varied widely, even when applied to similar diseases or dysfunctions.ConclusionsPeripheral magnetic stimulation is primarily used to treat musculoskeletal, neurological, and incontinence-related diseases, with outcomes centered on disease-specific assessments of muscle and physical function. However, its application in internal diseases remains limited, especially in cardiovascular disease, cancer, and diabetes mellitus. In addition, standardized peripheral magnetic stimulation prescriptions have not yet been established. Future studies should emphasize its implementation in underserved diseases and dysfunctions and establish standardized treatment protocols.

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https://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution Non-Commercial No Derivatives (CC BY-NC-ND) 4.0 License.

BACKGROUND

Neuromodulation is defined as the modification of neurological function, which includes neuron and glial cell activity, by delivering electric, magnetic, or chemical stimuli to specific neurologic target sites. 1 ) Magnetic stimulation, in particular, has garnered considerable attention as a therapeutic modality. This technique employs electromagnetic induction, whereby a pulsating magnetic field generated by a stimulation coil induces eddy currents within the body. 2 ) Magnetic stimulation, which evolved from transcranial magnetic stimulation first reported in humans in 1985, subsequently advanced into practical applications of repetitive stimulation. 3 ) Simultaneously, magnetic stimulation of peripheral nerves was introduced. 4 , 5 ) Peripheral magnetic stimulation (PMS) can stimulate deep motor and proprioceptive nerves without affecting superficial pain-sensitive nerves, because it does not directly affect cutaneous nociceptors. 6 ) PMS causes less pain and discomfort than electrical stimulation. 7 ) Furthermore, its ability to be applied over clothing without direct skin contact enhances its clinical application.

Pain, a key therapeutic target for PMS, acts by activating the supraspinal descending inhibition system. 8 ) Smania et al. 9 ) reported that PMS was more effective than transcutaneous electrical nerve stimulation (TENS) for treating myofascial pain. Furthermore, a meta-analysis indicated that PMS substantially reduced pain intensity in individuals with low back pain and knee osteoarthritis. 10 , 11 ) Despite limited evidence, PMS has proven effective in treating musculoskeletal pain and is generally well tolerated.

Despite its increasing use across various conditions, there is no consensus regarding the outcomes and effectiveness of PMS. Kamo et al. 12 ) investigated the effects of PMS on the activities of daily living (ADL) and physical function in individuals with stroke through a systematic review and meta-analysis, which demonstrated no substantial improvements in ADL, upper limb function, or muscle strength. Conversely, Chen et al. 13 ) reported that PMS may positively affect upper limb motor impairment, proximal upper limb muscle strength, and activity limitations in this population. Similarly, a systematic review concluded that PMS is a feasible, well-tolerated, and safe treatment option for muscle dysfunction in individuals with chronic obstructive pulmonary disease (COPD) 14 ) and may contribute to improved muscle strength. 15 , 16 ) However, only a few studies have examined the efficacy of PMS in this population, indicating a need for further research. 14 ) Previous randomized controlled trials have demonstrated positive effects of PMS across various conditions. Reported benefits include improved function in individuals with low back pain 17 ) ; enhanced vastus lateralis muscle strength, gait speed, and balance in individuals post-hip replacement 18 ) ; increased upper limb muscle strength in those with amyotrophic lateral sclerosis 19 ) ; improved pelvic floor muscle strength in those with postpartum pelvic floor dysfunction 20 ) ; enhanced cervical flexor muscle strength in healthy adults 21 ) ; and increased swallowing speed and capacity in individuals with stroke. 22 ) Conversely, no major effects of PMS on lower limb function have been observed in individuals with knee osteoarthritis. 23 )

The limited research and uncertainty regarding PMS effects on various dysfunctions and diseases likely stem from diversity in study populations (diseases), intervention settings, durations, and poorly defined outcomes. Meta-analyses on stroke survivors have yielded conflicting results, underscoring the need for additional studies with large sample sizes to strengthen the evidence. 12 , 13 ) Systematic reviews have focused on quadriceps function in individuals with COPD 14 ) and dysphagia across different populations. 24 ) However, the number of studies in these areas remains limited. Furthermore, previous systematic reviews and meta-analyses have provided limited coverage of disease types and functional impairments. In addition, organizing essential information for clinical application, such as PMS settings, outcomes, and treatment sites, has been challenging to synthesize comprehensively. Therefore, a comprehensive scoping review with a clear search strategy is warranted to provide a systematic overview of study populations (diseases), interventional content, and outcomes in existing studies and address the extensive evidence on PMS. Organizing this information is expected to clarify the diseases and functional impairments most appropriate for PMS application, as well as the relevant treatment settings and outcomes, thereby supporting more effective clinical practice. To date, however, no scoping review has been conducted to summarize the current clinical applications of PMS, and existing studies for future development remain unclear.

This scoping review aimed to identify, summarize, and map the relevant literature regarding the use of PMS for various diseases and related dysfunctions, highlighting areas for future research. Specifically, this scoping review addressed the following questions:

i) What types of diseases or populations have been treated with PMS?

ii) What are the treatment sites for PMS?

iii) What functional impairments are addressed through PMS?

iv) What outcomes are associated with PMS treatment?

v) What are the characteristics of PMS interventions, including frequency, intensity, stimulation session, duration, and overall treatment length?

METHODS

This scoping review was conducted in accordance with the Joanna Briggs Institute methodology for scoping reviews. 25 ) Reporting adhered to the Preferred Reporting Items for Systematic Reviews and Meta-Analysis extension for Scoping Reviews (PRISMA-ScR). 26 ) The protocol was registered with the Open Science Framework (https://osf.io/5q7mg/), and the corresponding protocol paper has been published. 27 )

Search Strategy

A search strategy was developed with an experienced research librarian to ensure thoroughness and precision in identifying relevant articles using key search terms. A systematic search of published literature from database inception to February 2024 was conducted. The databases searched included PubMed/MEDLINE, Cumulated Index to Nursing and Allied Health Literature (CINAHL) Complete, Cochrane Library, Web of Science, and PEDro. The search strategy was structured as follows: [(magnetic stimulation) AND (physical function)]. Detailed descriptions of the search terms and strategies applied to the databases are provided in Tables 1 – 4 .

Table 1.
Search strategy and results for PubMed/MEDLINE

Search numberQuerySearch detailsResults
1((((((“Muscle Strength”[Mesh]) OR “Gait”[Mesh]) OR “Sarcopenia/rehabilitation”[Mesh]) OR “Frailty/rehabilitation”[Mesh]) OR “Activities of Daily Living”[Mesh]) OR “Deglutition”[Mesh]) OR (“Deglutition Disorders/rehabilitation”[Mesh] OR “Deglutition Disorders/therapy”[Mesh])“Muscle Strength”[MeSH Terms] OR “Gait”[MeSH Terms] OR “sarcopenia/rehabilitation”[MeSH Terms] OR “frailty/rehabilitation”[MeSH Terms] OR “Activities of Daily Living”[MeSH Terms] OR “Deglutition”[MeSH Terms] OR “deglutition disorders/rehabilitation”[MeSH Terms] OR “deglutition disorders/therapy”[MeSH Terms]236,531
2dysphagia[Title/Abstract] OR deglutition[Title/Abstract] OR gait[Title/Abstract] OR muscle mass[Title/Abstract] OR sarcopenia[Title/Abstract] OR frailty[Title/Abstract] OR exercise capacity[Title/Abstract] OR walking test*[Title/Abstract] OR short physical performance battery[Title/Abstract] OR physical function*[Title/Abstract] OR disability[Title/Abstract] OR activities of daily living[Title/Abstract] OR swallowing function*[Title/Abstract] OR tongue pressure*[Title/Abstract] OR muscle strengt*[Title/Abstract]“dysphagia”[Title/Abstract] OR “deglutition”[Title/Abstract] OR “gait”[Title/Abstract] OR “muscle mass”[Title/Abstract] OR “sarcopenia”[Title/Abstract] OR “frailty”[Title/Abstract] OR “exercise capacity”[Title/Abstract] OR “walking test*”[Title/Abstract] OR “short physical performance battery”[Title/Abstract] OR “physical function*”[Title/Abstract] OR “disability”[Title/Abstract] OR “activities of daily living”[Title/Abstract] OR “swallowing function*”[Title/Abstract] OR “tongue pressure*”[Title/Abstract] OR “muscle strengt*”[Title/Abstract]464,185
3#1 OR #2“Muscle Strength”[MeSH Terms] OR “Gait”[MeSH Terms] OR “sarcopenia/rehabilitation”[MeSH Terms] OR “frailty/rehabilitation”[MeSH Terms] OR “Activities of Daily Living”[MeSH Terms] OR “Deglutition”[MeSH Terms] OR “deglutition disorders/rehabilitation”[MeSH Terms] OR “deglutition disorders/therapy”[MeSH Terms] OR “dysphagia”[Title/Abstract] OR “Deglutition”[Title/Abstract] OR “Gait”[Title/Abstract] OR “muscle mass”[Title/Abstract] OR “sarcopenia”[Title/Abstract] OR “frailty”[Title/Abstract] OR “exercise capacity”[Title/Abstract] OR “walking test*”[Title/Abstract] OR “short physical performance battery”[Title/Abstract] OR “physical function*”[Title/Abstract] OR “disability”[Title/Abstract] OR “Activities of Daily Living”[Title/Abstract] OR “swallowing function*”[Title/Abstract] OR “tongue pressure*”[Title/Abstract] OR “muscle strengt*”[Title/Abstract]606,783
4“Magnetic Field Therapy”[Mesh:NoExp]“Magnetic Field Therapy”[MeSH Terms:noexp]1309
5peripheral magnetic stimulation[Title/Abstract] OR rpms[Title/Abstract] OR magnetic treatment*[Title/Abstract] OR magnetotherapy[Title/Abstract] OR magnetic field therap*[Title/Abstract]“peripheral magnetic stimulation”[Title/Abstract] OR “rpms”[Title/Abstract] OR “magnetic treatment*”[Title/Abstract] OR “magnetotherapy”[Title/Abstract] OR “magnetic field therap*”[Title/Abstract]923
6#4 OR #5“Magnetic Field Therapy”[MeSH Terms:noexp] OR “peripheral magnetic stimulation”[Title/Abstract] OR “rpms”[Title/Abstract] OR “magnetic treatment*”[Title/Abstract] OR “magnetotherapy”[Title/Abstract] OR “magnetic field therap*”[Title/Abstract]2117
7#3 AND #6(“Muscle Strength”[MeSH Terms] OR “Gait”[MeSH Terms] OR “sarcopenia/rehabilitation”[MeSH Terms] OR “frailty/rehabilitation”[MeSH Terms] OR “Activities of Daily Living”[MeSH Terms] OR “Deglutition”[MeSH Terms] OR (“deglutition disorders/rehabilitation”[MeSH Terms] OR “deglutition disorders/therapy”[MeSH Terms]) OR (“dysphagia”[Title/Abstract] OR “Deglutition”[Title/Abstract] OR “Gait”[Title/Abstract] OR “muscle mass”[Title/Abstract] OR “sarcopenia”[Title/Abstract] OR “frailty”[Title/Abstract] OR “exercise capacity”[Title/Abstract] OR “walking test*”[Title/Abstract] OR “short physical performance battery”[Title/Abstract] OR “physical function*”[Title/Abstract] OR “disability”[Title/Abstract] OR “Activities of Daily Living”[Title/Abstract] OR “swallowing function*”[Title/Abstract] OR “tongue pressure*”[Title/Abstract] OR “muscle strengt*”[Title/Abstract])) AND (“Magnetic Field Therapy”[MeSH Terms:noexp] OR (“peripheral magnetic stimulation”[Title/Abstract] OR “rpms”[Title/Abstract] OR “magnetic treatment*”[Title/Abstract] OR “magnetotherapy”[Title/Abstract] OR “magnetic field therap*”[Title/Abstract]))173
8#7 AND English[Language](“Muscle Strength”[MeSH Terms] OR “Gait”[MeSH Terms] OR “sarcopenia/rehabilitation”[MeSH Terms] OR “frailty/rehabilitation”[MeSH Terms] OR “Activities of Daily Living”[MeSH Terms] OR “Deglutition”[MeSH Terms] OR (“deglutition disorders/rehabilitation”[MeSH Terms] OR “deglutition disorders/therapy”[MeSH Terms]) OR (“dysphagia”[Title/Abstract] OR “Deglutition”[Title/Abstract] OR “Gait”[Title/Abstract] OR “muscle mass”[Title/Abstract] OR “sarcopenia”[Title/Abstract] OR “frailty”[Title/Abstract] OR “exercise capacity”[Title/Abstract] OR “walking test*”[Title/Abstract] OR “short physical performance battery”[Title/Abstract] OR “physical function*”[Title/Abstract] OR “disability”[Title/Abstract] OR “Activities of Daily Living”[Title/Abstract] OR “swallowing function*”[Title/Abstract] OR “tongue pressure*”[Title/Abstract] OR “muscle strengt*”[Title/Abstract])) AND (“Magnetic Field Therapy”[MeSH Terms:noexp] OR (“peripheral magnetic stimulation”[Title/Abstract] OR “rpms”[Title/Abstract] OR “magnetic treatment*”[Title/Abstract] OR “magnetotherapy”[Title/Abstract] OR “magnetic field therap*”[Title/Abstract])) AND “English”[Language]155
9(animals[MeSH Terms]) NOT (humans[MeSH Terms])“animals”[MeSH Terms] NOT “humans”[MeSH Terms]5,189,739
10#8 NOT #9((“Muscle Strength”[MeSH Terms] OR “Gait”[MeSH Terms] OR “sarcopenia/rehabilitation”[MeSH Terms] OR “frailty/rehabilitation”[MeSH Terms] OR “Activities of Daily Living”[MeSH Terms] OR “Deglutition”[MeSH Terms] OR (“deglutition disorders/rehabilitation”[MeSH Terms] OR “deglutition disorders/therapy”[MeSH Terms]) OR (“dysphagia”[Title/Abstract] OR “Deglutition”[Title/Abstract] OR “Gait”[Title/Abstract] OR “muscle mass”[Title/Abstract] OR “sarcopenia”[Title/Abstract] OR “frailty”[Title/Abstract] OR “exercise capacity”[Title/Abstract] OR “walking test*”[Title/Abstract] OR “short physical performance battery”[Title/Abstract] OR “physical function*”[Title/Abstract] OR “disability”[Title/Abstract] OR “Activities of Daily Living”[Title/Abstract] OR “swallowing function*”[Title/Abstract] OR “tongue pressure*”[Title/Abstract] OR “muscle strengt*”[Title/Abstract])) AND (“Magnetic Field Therapy”[MeSH Terms:noexp] OR (“peripheral magnetic stimulation”[Title/Abstract] OR “rpms”[Title/Abstract] OR “magnetic treatment*”[Title/Abstract] OR “magnetotherapy”[Title/Abstract] OR “magnetic field therap*”[Title/Abstract])) AND “English”[Language]) NOT (“animals”[MeSH Terms] NOT “humans”[MeSH Terms])146

Table 2.
Search strategy and results for Cochrane Library

Search numberSearchHits
1MeSH descriptor: [Magnetic Field Therapy] this term only224
2(“peripheral magnetic stimulation”):ti,ab,kw OR (rpms):ti,ab,kw OR (magnetic NEXT treatment*):ti,ab,kw OR (magnetotherapy):ti,ab,kw OR (magnetic NEXT field NEXT therap*):ti,ab,kw584
3#1 OR #2584
4MeSH descriptor: [Muscle Strength] explode all trees8775
5MeSH descriptor: [Gait] explode all trees3330
6MeSH descriptor: [Sarcopenia] explode all trees and with qualifier (s): [rehabilitation − RH]22
7MeSH descriptor: [Frailty] explode all trees and with qualifier (s): [rehabilitation − RH]19
8MeSH descriptor: [Activities of Daily Living] explode all trees13,153
9MeSH descriptor: [Deglutition] explode all trees606
10MeSH descriptor: [Deglutition Disorders] explode all trees and with qualifier (s): [therapy − TH, rehabilitation − RH]579
11{OR #4-#10}25,152
12(dysphagia):ti,ab,kw OR (deglutition):ti,ab,kw OR (gait):ti,ab,kw OR (“muscle mass”):ti,ab,kw OR (sarcopenia):ti,ab,kw26,034
13(frailty):ti,ab,kw OR (“exercise capacity”):ti,ab,kw OR (walking NEXT test*):ti,ab,kw OR (“short physical performance battery”):ti,ab,kw OR (physical NEXT function*):ti,ab,kw26,943
14(disability):ti,ab,kw OR (“activities of daily living”):ti,ab,kw OR (swallowing NEXT function*):ti,ab,kw OR (tongue NEXT pressure*):ti,ab,kw OR (muscle NEXT strengt*):ti,ab,kw76,574
15{OR #12-#14}114,236
16#11 OR #15121,461
17#3 AND #16121

Table 3.
Search strategy and results for CINAHL Complete

Search numberQueryResults
S01(MH “Magnet Therapy”)1299
S02“peripheral magnetic stimulation” OR rpms OR magnetic W0 treatments OR magnetotherapy OR magnetic W0 field W0 therap*1834
S03S1 OR S22278
S04(MH “Muscle Strength+”)30,938
S05(MH “Gait+”)15,360
S06(MH “Sarcopenia/RH”)64
S07(MH “Frailty Syndrome/RH”)54
S08(MH “Activities of Daily Living+”)80,445
S09(MH “Deglutition”)4382
S10(MH “Deglutition Disorders/RH/TH”)754
S11dysphagia OR deglutition OR gait OR “muscle mass” OR sarcopenia OR frailty OR “exercise capacity” OR walking W0 tests OR “short physical performance battery” OR physical W0 function* OR disability OR “activities of daily living”325,166
S12swallowing W0 function* OR tongue W0 pressure* OR muscle W0 strength*40,789
S13S4 OR S5 OR S6 OR S7 OR S8 OR S9 OR S10 OR S11 OR S12399,781
S14S3 AND S13217
S15S3 AND S13 (English only)210

Table 4.
Search strategy and results for Web of Science Core Collection and PEDro

DatabaseSearch numberSearch queryResults
Web of Science Core Collection
1((((((((((((((TS=(muscle NEAR/0 strength)) OR TS=(gait)) OR TS=(sarcopenia)) OR TS=(frailty)) OR TS=(“activities of daily living”)) OR TS=(deglutition)) OR TS=(dysphagia)) OR TS=(muscle NEAR/1 mass)) OR TS=(exercise NEAR/0 capacity)) OR TS=(walking NEAR/0 test*)) OR TS=(“short physical performance battery”)) OR TS=(physical NEAR/0 function*)) OR TS=(disability)) OR TS=(swallowing NEAR/0 function*)) OR TS=(tongue NEAR/0 pressure*)494,491
2(((TS=(magnetic NEAR/0 field NEAR/0 therapy)) OR TS=(“peripheral magnetic stimulation”)) OR TS=(magnetic NEAR/1 treatment*)) OR TS=(magnetotherapy)3128
3#1 AND #2115
4#1 AND #2 and Proceeding Paper (Exclude − Document Types)112
5#1 AND #2 and Proceeding Paper (Exclude − Document Types) and English (Languages)111
PEDro
1magnetic stimulation (abstract & title)216

Study Selection and Eligibility Criteria

Studies were selected using a three-step process that involved managing search results, removing duplicates, screening titles and abstracts, and conducting full-text reviews. The inclusion criteria were as follows: 1) randomized controlled trials, observational studies, case series, and case reports; 2) original human studies; 3) publication in English; and 4) studies examining the effects of PMS on physical function. Conference abstracts, review articles, and editorials were excluded. Reference lists of review articles were evaluated, and relevant studies were extracted. After removing duplicates, two reviewers (TF and JN) independently evaluated study eligibility by reviewing the titles and abstracts based on the inclusion criteria. Full-text articles were reviewed to confirm eligibility or when abstracts and titles lacked sufficient information. Any disagreements were resolved by consensus, and if consensus could not be reached, a third reviewer was consulted. The final inclusion of eligible studies was determined through consensus meetings involving all authors.

Data Extraction

Data were extracted using a chart table developed by the authors. Two reviewers (TF and JN) extracted the following data from each study: 1) first author’s last name, 2) publication year, 3) nationality, 4) study design, 5) disease, 6) number of participants, 7) age, 8) sex, 9) functional impairment, 10) treatment site, 11) PMS treatment details (including frequency, intensity, stimulation session, and duration), 12) outcomes, and 13) main results. When necessary, the authors were contacted for further information and data clarification. 28 )

Data Presentation

Data are presented in tables and figures, along with a narrative summary aligned with the objectives and scope of this review. Online tools were used to generate some figures (https://www.mapchart.net/).

RESULTS

The initial literature search identified 804 articles, which were reduced to 634 after excluding duplicates. Title and abstract screening identified 124 eligible articles for full-text review. In addition, reference lists from 27 review articles were screened. Ultimately, 97 articles were identified as suitable for this scoping review ( Fig. 1 ).

Fig. 1. Flowchart of study screening process.
Fig. 1. Flowchart of study screening process.

Study Overview

Characteristics of the included studies are summarized in Table 5 . All included articles were published after 1993. In total, 15 studies were conducted in Turkey 29 , 30 , 31 , 32 , 33 , 34 , 35 , 36 , 37 , 38 , 39 , 40 , 41 , 42 , 43 ) ; 10 in the United States 44 , 45 , 46 , 47 , 48 , 49 , 50 , 51 , 52 , 53 ) ; 9 in Italy 19 , 54 , 55 , 56 , 57 , 58 , 59 , 60 , 61 ) ; 8 in Japan 21 , 22 , 62 , 63 , 64 , 65 , 66 , 67 ) ; 7 in Germany 68 , 69 , 70 , 71 , 72 , 73 , 74 ) ; 6 in Canada 75 , 76 , 77 , 78 , 79 , 80 ) and South Korea 17 , 18 , 23 , 81 , 82 , 83 ) ; 5 in China 20 , 84 , 85 , 86 , 87 ) ; 4 in Egypt 88 , 89 , 90 , 91 ) and Poland 92 , 93 , 94 , 95 ) ; 2 in New Zealand, 96 , 97 ) Saudi Arabia, 98 , 99 ) Slovenia, 100 , 101 ) Spain, 15 , 16 ) the United Kingdom, 102 , 103 ) and Brazil 104 , 105 ) ; and 1 in Australia, 106 ) Austria, 107 ) Denmark, 108 ) Iran, 109 ) Israel, 110 ) Lithuania, 111 ) Nigeria, 112 ) Romania, 113 ) Russia, 114 ) Singapore, 115 ) and Switzerland ( Fig. 2 ). 116 )

Table 5.
Characteristics of included studies
10MWT, 10-m walk test; 3MWT, 3-min walking test; 5TST, five times Sit-to-Stand test; ALS, amyotrophic lateral sclerosis; BBS, Berg balance scale; BBT, box and block test; BI, Barthel Index; CMS, Constant Murley Score; CRPS, Complex Regional Pain Syndrome; DASH, disabilities of the arm, shoulder, and hand; ELF-EMF, extremely low frequency electromagnetic field; ExMI, extracorporeal magnetic innervation; FAC, functional ambulation category; FFMI, fat free mass index; FIM, functional independence measure; FIQ, Fibromyalgia Impact Questionnaire; FMS, functional magnetic stimulation; HAQ, Health Assessment Questionnaire; HIFEM, high-intensity focused electromagnetic field; KOOS, Knee Injury and Osteoarthritis Score; LE-FMA, lower-extremity Fugl-Meyer Assessment; MRC, Medical Research Council; MRI, magnetic resonance imaging; NA, not available; NPDS, Neck Pain and Disability Scale;; NRCT, non-randomized controlled trial; MS, magnetic stimulation; PEME, pulsed electromagnetic energy; PEMF, pulsed electromagnetic field therapy; PEMT, pulsed electromagnetic therapy; PFDI, Pelvic Floor Disability Index; PMF, pulsed magnetic field; PSFS, Patient-specific Functional Scale; RCT, randomized controlled trial; RMDQ-24, Roland-Morris Disability Questionnaire-24; SPADI, Shoulder Pain and Disability Index; TUG, Timed Up-and-Go test; UCLA, University of California Los Angeles; UES, upper oesophageal sphincter; WFMT, Wolf motor function test.

Author, yearCountryStudy designPopulation (disease, number, gender, age)Functional impairmentTreatment sitePMS (frequency, intensity, stimulation session, duration)OutcomesMain results
Abdelhalim et al., 2019Saudi ArabiaNRCTLow back pain n=42 Female, 33.3% Age: PEMF: 37.03±6.74 years Sham: 36.85±7.14 yearsPain and dysfunctionLow backPEMF 5–10 Hz frequency Intensity: patient tolerance Three sessions/week 4 weeks∙ Modified ODI ∙ Modified Schober testAll outcome measures were significantly improved statistically in the experimental group at the end of the intervention. There were non-significant differences in all outcome measures in the sham group.
Afzalifard et al., 2022IranRCTShoulder Impingement Syndrome n=60 Female, NA Age: NAShoulder pain and disabilityShoulderMagnet therapy 18 Hz frequency 100 Hz frequency Intensity: 100 mT 30 min/session Three times/week 4 weeks∙ DASH ∙ Active ROMUsing magnet therapy with two frequencies of 18 and 100 Hz along with routine electrotherapy and exercise therapy had no additional positive effect on the recovery process of patients with shoulder impingement syndrome.
Alazab et al., 2022EgyptRCTStroke n=60 Female, 40.0% Age: NAShoulder subluxation-related dysfunctionShoulderrPMS 30 Hz frequency Intensity: not reported Two times/week 2 months∙ UE-FMAA significant increase detected in UE-FMA for rPMS in comparison with control after treatment (P=0.03).
Alzayed and Alsaadi, 2020Saudi ArabiaRCTLow back pain n=42 Female, 47.6% Age: PEMF: 41.45±9.45 years Sham: 42.61±9.69 yearsLow back painLow backPEMF Strong intensity 20 min∙ RMDQ-24Treatment group experienced a faster improvement in disability than the placebo group. Analysis showed a significant improvement in the disability scores in the treatment group at week 3, whereas an improvement in the placebo group was detected at week 6. Significant improvement in both groups was sustained for weeks 6, 9, and 13. There was no difference between the groups in scores of disability at weeks 6 and 13.
Ay and Evcik, 2009TurkeyRCTKnee osteoarthritis n=55 Female, PEMF: 70% Placebo: 76% Age: PEMF: 58.9±8.8 years Placebo: 57.7±6.5 yearsPain and dysfunctionKneePEMF 50 Hz frequency Intensity: 105 μT 30 min/session Five times/week 3 weeks∙ ROM ∙ Lequesne Algofunctional Index of kneeStatistically significant improvement was observed in some of the subgroups of Lequesne index including ADL compared to placebo. No statistically significant difference in total of the scale between two groups. Between-group analysis showed no beneficial symptomatic effect of PEMF in the treatment of knee OA in all patients.
Aydin et al., 2018TurkeyRCTLumbar spinal stenosis n=49 Female, PEMF: 72.0% Placebo: 70.8% Age: PEMF: 61.6±8.6 years Placebo: 64.6±5.0 yearsChronic back painBackPEMF 25 Hz frequency Intensity: 80 G 15 min/session Five sessions/week 2 weeks∙ ODI ∙ TUGPEMF appears to be useful in terms of functional mobility and physical disability in lumbar spinal stenosis patients.
Baek et al., 2018KoreaRCTHip replacement after proximal femur fracture n=22 Female, 86.4% Age: rPMS: 77.09±6.78 years Sham: 80.36±7.97 yearsMuscle dysfunctionVastus lateralisrPMS 10 Hz (on time: 1.5 s, off time: 6 s) frequency Intensity: visible movement of the knee is triggered 25 min 15 sessions Five times per week 3 weeks∙ Vastus lateralis strength ∙ Tandem test ∙ Gait speedBoth RMS value of the vastus lateralis and the ratio of RMS values after rPMS were significantly improved. Tandem standing time and usual gait speed in rPMS group were significantly increased.
Bagnato et al., 2016ItalyRCTKnee osteoarthritis n=60 Female, 71.7% Age: 67.7±10.9 yearsKnee painKneePEMF 27.12 Hz frequency Peak burst output power of the 12-cm antenna is 0.0098 W Minimum 12 h at night 1 month∙ WOMACPEMF induced a significant improvement in WOMAC scores compared with placebo.
Beaulieu et al., 2015CanadaRCTChronic stroke n=18 Female, 61.1% Age: rPMS: 51±15 years Sham: 55±11 yearsAnkle impairmentsParetic tibialis anteriorrPMS Theta-burst frequency: 5-Hz bursts of three 50-Hz pulses each (2 s on, 8 s off) Intensity: 42% of the maximal stimulator output 190 s One session∙ Active/passive ROM (dorsiflexion) ∙ Isometric muscle strength (dorsiflexion)In the rPMS group, ankle dorsiflexion mobility and maximal isometric strength increased.
Beaulieu et al., 2017CanadaCrossover RCTChronic stroke n=15 Female, 30.8% Age: 51.1±15.9 yearsSensorimotor impairmentsParetic ankle musclesrPMS 20 Hz (on: 3 s, off: 19 s) frequency Intensity: inducing the maximal amplitudes of dorsiflexion/eversion 40 repetitions One session∙ Active/passive ROM (dorsiflexion, foot evertors) ∙ Isometric muscle strength (dorsiflexion, foot evertors)Ankle muscle strength was significantly improved by rPMS.
Benedetti et al., 2020ItalyRCTType I CRPS n=30 Female, 90.0% Age: Treatment: 56.6±10.4 years Control: 56.8±14.1 yearsPain and functional declineWhole body, handBio-electro-magnetic-energy-regulation Low frequency (<33.3 Hz) Intensity: 7–35µT 20 min/session 10 consecutive days∙ Handgrip strength ∙ DASH ∙ Maryland Foot ScoreThe treatment group yielded better results in the short term, in terms of pain reduction and functional improvement in both the upper and lower limbs.
Bonfert et al., 2023GermanyCase reportCerebral palsy n=1 Male Age: 8 yearsMotor impairmentGluteal musclesFunctional repetitive neuromuscular magnetic stimulation 25 and 35 Hz frequency Intensity: 3 T 45 min/session 12 sessions 3 weeks∙ Gross motor function measure ∙ 10MWT ∙ Balance assessment (posturography)At day 4 after the intervention, the patient reported clinical benefits and improvements of standing and walking assessed by Gross Motor Function Measure dimensions. Body sway as measured by center of pressure displacement during posturography decreased.
Bustamante et al., 2008SpainRCTCOPD n=15 Female, 0.0% Age: MS: 59±8 years Control: 68±10 yearsMuscle dysfunctionQuadricepsMS 15–8 Hz frequency Intensity: 40%–70% of the maximal output of the stimulator 15 min/session 3 days/week 3 weeks∙ FFMI ∙ 6MWT ∙ Proportion of type I muscle fibers (biopsy)Compared to controls, magnetic stimulation muscle training induced a significant increase in type I fiber size.
Bustamante et al., 2010SpainRCTCOPD n=18 Female, 0% Age: rPMS: 61±6 years Control: 62±8 yearsMuscle dysfunctionQuadriceps musclerPMS 15 Hz frequency Intensity: 40% of the maximum stimulation (2T) Intensity was increased by 2%–3% every two sessions, ending the protocol at an intensity of 70% at 7 Hz 15 min/session Three times/week 8 weeks∙ FFMI ∙ Quadriceps strength ∙ 6MWTAll patients completed the training with increasing intensity of stimulation, displaying a significant improvement in voluntary quadriceps strength (17.5% of the baseline value) and exercise capacity, with a mean increase of 23 m in the 6MWT.
But, 2003SloveniaRCTWomen with urinary incontinence n=52 Female, 100% Age: 55.8 (34–78) yearsUrinary incontinencePelvic floor muscleFMS 10 Hz frequency Intensity: 10 µT Wearing the device day and night 2 months∙ Pelvic floor muscle power ∙ Time of pelvic floor muscle contractionsIn patients from the active group, significant improvements were observed in the power of the pelvic floor muscle contractions (P=0.0071) and in the duration of the pelvic floor muscle contractions (P=0.038).
Bölükbaş et al., 2005TurkeyNRCTUrinary incontinence n=22 Female, 100.0% Age: 47.91±11.1 yearsUrinary incontinencePelvic floorFMS 10, 50 Hz frequency 20 min/session Two sessions/week 6 weeks∙ Pelvic floor muscle strengthThe pelvic floor muscle strength increased significantly during stimulation compared with prestimulation.
Callaghan et al., 2005UKRCTKnee osteoarthritis n=27 Female, 48.1% Age: High dose: 58.3±7.3 years Low dose: 59.5±6.7 years Placebo: 63.5±7.9 yearsPain and dysfunctionKneePulsed short wave 27 MHz frequency Intensity: 10 or 20 W 20 min/session Six sessions 2 weeks∙ ROM ∙ Quadriceps muscle strength ∙ Walking speedFunctional measures revealed no pre- and post-treatment differences between the groups (P >0.05), except for improved knee ROM in the placebo group (P <0.05).
Chen et al., 2020ChinaNRCTStroke n=32 Female, 28.1% Age: rPMS: 49.0±18.2 years Sham: 45.6±8.3 yearsStroke-related upper-extremity dysfunctionUpper extremity: shoulder joint (proximal joint) to the wrist joint (distal joint)rPMS 5 Hz frequency (muscle groups with spasticity) 20 Hz frequency (antagonistic muscles) MAS score of the antagonistic muscle was 1, a 5-Hz stimulation was still used. Intensity: 100% of the muscle contraction threshold at a resting state 30 min Single session∙ UE-FMAUE-FMA was improved (P <0.05) after single session of rPMS.
Cichoń et al., 2017PolandRCTIschemic stroke n=57 Female, Study: 64.8% Control: 65.6% Age: Study: 68.0±15.6 years Control: 70.9±15.3 yearsPost-ischemic stroke conditionPelvic girdlePEMF 40 Hz frequency Intensity: 7 mT 15 min 5 days/week 4 weeks∙ BIResults show that ELF-EMF induced a significant improvement in ADL.
Cichoń et al., 2018PolandRCTStroke n=57 Female, Study: 64.8% Control: 65.6% Age: Study: 68.0±15.6 years Control: 70.9±15.3 yearsPost-acute stroke conditionPelvic girdlePEMF 40 Hz Intensity: 5 mT 15 min 5 days/week 4 weeks∙ BIThe ADL value in patients treated with ELF-EMF increased by about 25% compared with the control group.
Culligan et al., 2005USARCTPrimiparous n=51 Female, 50.0% Age: 64.14±13.61 yearsPelvic floor dysfunctionPelvic floorExMI 50 Hz frequency 20 min/session Two sessions/week 8 weeks∙ Pelvic floor muscle strengthNo differences in pelvic muscle strength between patients receiving active or sham ExMI treatments in the early postpartum period.
Cömertoğlu et al., 2022TurkeyRCTCRPS-1 n=32 Female, 50.0% Age: 50.1±13.1 yearsPain and dysfunctionHandPEMF 8 Hz frequency Intensity: 3.2 mT 75–95 min/session Five times/week 4 weeks∙ Handgrip strength ∙ Pinch strength ∙ Moberg pick up test ∙ Duruöz Hand IndexPEMF in addition to conventional rehabilitation did not provide additional benefit for pain and hand functions in CRPS-1.
Dudonienė et al., 2023LithuaniaRCTWomen with stress urinary incontinence n=48 Female, 100.0% Age: FMS: 40.25±6.49 years Pelvic floor muscle training: 37.58±5.86 yearsStress urinary incontinencePelvic floor muscleFMS 35 (first 20 min)→5 (last 10 min) Hz frequency Intensity: not reported 30 min/session 12 sessions Two times/week 6 weeks∙ Pelvic floor muscle strength ∙ Pelvic floor muscle endurancePelvic floor muscle strength and endurance increased (P <0.05) in both groups with a medium (d=0.52) to large (d=1.56) effect size.
Dündar et al., 2016TurkeyRCTKnee osteoarthritis n=40 Female, 72.5% Age: PEMF: 56.8±14.5 years Sham: 57.6±13.8 yearsPain and dysfunctionKneePEMF 50 Hz frequency Intensity: 100 µT 20 min/session Five sessions/week 4 weeks∙ WOMACWOMAC scores significantly improved in both treatment groups. There was no overall statistically significant difference between the groups.
Elshiwi et al., 2019EgyptRCTLow back pain n=50 Female, PEMF: 48.0% Control: 52.0% Age: PEMF: 36.73±2.52 years Control: 37.27±2.52 yearsPain and dysfunctionLow backPEMF 50 Hz frequency Intensity: 20 Gauss 20 min/session Three times/week 4 weeks∙ ODI ∙ ROMAdding pulsed electromagnetic field to conventional physical therapy yields superior clinical improvement in pain, functional disability, and lumbar ROM in patients with non-specific low back pain when compared with conventional physical therapy alone.
Fary et al., 2011AustraliaRCTKnee osteoarthritis n=70 Female, 47.1% Age: Active: 70.7±8.9 years Placebo: 68.9±11.4 yearsPain and dysfunctionKneePulsed electrical stimulation 100 Hz frequency Intensity: NA 7 h/day 26 weeks∙ WOMAC ∙ Parous women activity profile ∙ ActigraphThere were no differences between groups for changes in WOMAC or activity measures.
Fawaz et al., 2023EgyptRCTPost-stroke n=80 Female, 30.0% Age: 57.33±10.67 yearsPost-stroke hemiparesisShoulder abductors, elbow extensors, wrist extensors, supinator musclerPMS 30 Hz frequency Intensity: 10% above the level that evoked wrist movement taken at rest (average for all cases was between 35% and 45%) 30 min/ whole session Five sessions/week 3 weeks∙ UE-FMA ∙ Extensor digitorum muscle cross-sectional area ∙ FIM ∙ Active ROMPost rehabilitation program, UE-FMA and FIM both showed highly significant improvement in the active group compared to controls. Regarding active ROM of the shoulder abductors, triceps, wrist extensors, and supinators, significant differences were found in the active group in comparison to controls.
Flamand and Schneider, 2014CanadaCase reportCerebral palsy n=1 Female, 0% Age: 7 yearsMotor deficitsSciatic and tibial nerves and over the common peroneal nerverPMS Three pulses at 50 Hz, repeated every 200 ms (5 Hz) Intensity: palpable muscle contractions and ankle movements Sciatic nerve: 180 s Tibial nerve: 60 s Common peroneal nerve: 2 s trains of pulses repeated every 10 s during 300 s Five rPMS sessions (S1-S5, each successive Thursday and Tuesday)∙ Active/passive ROM (dorsiflexion) ∙ Gait (walking velocity, stride length, cadence, cycle duration)An increase of active dorsiflexion range of movement and increased gait parameters were observed.
Fujimura et al., 2020JapanPre–post, single-arm studyStroke n=12 Female, 41.7% Age: 61±17 yearsShoulder subluxationsShoulder (supraspinatus and posterior deltoid/infraspinatus muscles)rPMS 30 Hz (on: 2 s, off: 3 s) frequency 17 min/day 5 days/week 4 weeks∙ Active ROM (shoulder abduction) ∙ UE-FMAActive ROM of shoulder abduction and UE-FMA improved significantly after treatment.
Fukuda et al., 2011BrazilRCTKnee osteoarthritis n=112 Female, 100.0% Age: High dose: 63.0±9.0 years Low dose: 62.0±8.0 years Placebo: 57.0±9.0 years Control: 61.0±10.0 yearsPain and dysfunctionKneePulsed short wave 145 Hz frequency Intensity: 14.5 W 19 or 38 min/session Three sessions/week 3 weeks∙ KOOSBoth treatment groups showed a significant improvement in function compared with the control and placebo groups. There were no differences in results between doses, although a low dose appeared to be more effective in the long term.
Galace de Freitas et al., 2014BrazilRCTShoulder impingement syndrome n=56 Female, 64.3% Age: 50.5±8.9 yearsPain and muscle dysfunctionShoulderPEMF 50 Hz frequency Intensity: 20mT or 200G 30 min Three times/week 3 weeks∙ CMS ∙ UCLA ∙ Shoulder lateral rotation muscle strength ∙ Shoulder medial rotation muscle strength ∙ Shoulder elevation muscle strengthPatients in the active PEMF group had a higher level of function at all follow-up time frames compared with baseline. PEMF group had increased strength for lateral rotation at 9 weeks, and increased strength for medial rotation at 9 weeks and 3 months when compared with baseline.
Galovic et al., 2018SloveniaRCTLow back pain n=60 Female, 58.3% Age: PEMF: 57.45±11.55 years Placebo: 11.05±10.71 yearsPain and dysfunctionLow backPEMF 10 Hz frequency Intensity: 50% of maximum intensity 20 min/session Five sessions/week 3 weeks∙ ODIIn both groups, the level of the function assessed with the ODI improved immediately after the therapy and 1 month after the completed therapy, but the differences among groups were not statistically significant.
Garland et al., 2007USARCTKnee osteoarthritis n=58 Female, 65.5% Age: Active: 64.3±10.2 years Placebo: 69.9±11.4 yearsPain and dysfunctionKneePulsed electrical stimulator 100 Hz frequency Intensity: 12 V 6 h/day 3 months∙ WOMACActive treatment provided superior outcomes between baseline and 3-month follow-up measurements in WOMAC function.
Gilling et al., 2009New ZealandRCTStress urinary incontinence n=70 Female, 100.0% Age: Intervention: 54.0±2.0 years Sham: 54.8±2.2 yearsStress urinary incontinencePelvic floorElectromagnetic stimulation 10, 50 Hz frequency 20 min/session Three sessions/week 8 weeks∙ Pelvic floor muscle strengthThere was a statistically significant improvement in the active arm at 8 weeks in pelvic floor muscle strength. There was no significant difference between the groups.
Giusti et al., 2013ItalyRCTOlder adults with low bone mineral density n=41 Female, 7.3% Age: PEMF: 84 (74–96) years Placebo: 87 (75–100) yearsLow physical performanceWhole bodyPEMF Low-power laser: wavelength 500–700 nm Low-energy infrared pulsed light: wavelength 700–1050 nm TENS: maximum amplitude 200 V 10 min One session∙ Gait speedIn the intervention group, self-selected gait speed increased significantly from baseline. In the placebo group, all gait parameters except for support base remained unchanged.
Giusti et al., 2014ItalyRetrospective, single-arm studyOlder adults n=266 Female, 91% Age: 77.1±5.6 yearsHistory of fallsWhole bodyPEMF Low-power laser: wavelength 500–700 nm Low-energy infrared pulsed light: wavelength 700–1050 nm TENS: maximum amplitude 200 V 10 min Every 2 months 1 year∙ Gait speedThe results suggest that continuous exposure to PEMF improves self-selected gait speed in older adults at risk of falling.
Gremion et al., 2009SwitzerlandRCTKnee osteoarthritis n=89 Female, 44.9% Age: Pulsed signal therapy: 58±13 years Physiotherapy: 61±8 yearsDisabilityKneePulsed signal therapy 15 Hz frequency Intensity: 12.5G 60 min/session 9 days∙ Knee ROM ∙ Lequesne Index of SeverityBoth treatments resulted in significant improvements in pain and physical function. A statistical difference was observed only for ADL, where the physiotherapy was more efficient.
Grosse et al., 2023GermanyProspective, pre–post, single-arm studyCerebral palsy n=8 Female, 62.5% Age: 10.4±2.5 yearsMotor impairmentGluteal musclesFunctional repetitive neuromuscular magnetic stimulation 25 and 35 Hz frequency Intensity: 3 T 20 min/session 12 sessions 3 weeks∙ Canadian Occupational Performance MeasureThe Canadian Occupational Performance Measure demonstrated clinically important benefits for performance in 28%. Functional repetitive neuromuscular magnetic stimulation is a safe and well-accepted neuromodulatory approach that could improve the activity and participation of children and adolescents with bilateral spastic cerebral palsy.
Gumussoy et al., 2021TurkeyRCTStress incontinence n=51 Female, 100.0% Age: 50.92±8.88 yearsStress incontinencePelvic floor muscleExMI 10 and 50 Hz frequency Intensity: NA 20 min/session Two times/week 8 weeks∙ Pelvic floor muscle contraction forceFindings indicate that use of magnetic innervation does not improve pelvic floor muscle strength when compared to pelvic floor muscle training alone.
Hattapoğlu et al., 2019TurkeyRCTCervical disc herniation n=64 Female, 28.1% Age: PEMF: 42.96±10.35 years Sham: 47.15±11.03 yearsNeck pain and disabilityCervical regionPEMF 50 Hz frequency Intensity: 0.6 mT 20 min 5 days/week 3 weeks∙ NPDSA significant improvement was found in the disability of both groups after treatment when compared to those before treatment.
Iannitti et al., 2013USAPre–post, two-arm studyKnee osteoarthritis n=28 Female, NA Age: 69.9±1.5 yearsPain and muscle dysfunctionKneePEMF 6–100 Hz (low frequency) and 500–2000 Hz (high frequency) for 15 min, and 6–100 Hz (low frequency) and 100–5000 Hz (high frequency) for 15 min Intensity: 50–100G 30 min Three times/week 6 weeks∙ WOMACPEMF therapy improves physical function in elderly patients affected by knee osteoarthritis.
Jiang et al., 2022ChinaRCTSubacute stroke n=44 Female, 38.6% Age: rPMS: 54.62±10.89 years Control: 56.09±16.59 yearsSevere upper-extremity impairmentTriceps brachii, extensor digitorumrPMS 20 Hz stimulation for 0.5 s per session, with a 2-s interval between sessions, 120 sessions per muscle, a total of 2400 pulses per treatment Triceps brachii: Intensity gradually increased from 0% of maximum output until 30° elbow extension was induced Extensor digitorum: Intensity gradually increased from 0% until wrist joint was extended by 45° Daily 2 weeks∙ UE-FMAThe rPMS group showed more significant improvements in the FMA.
Kagaya et al., 2019JapanPre–post, single-arm studyHealthy volunteers n=11 Female, 0% Age: 32±9 yearsDysphagiaSuprahyoid musclesrPMS 30 Hz (on: 2 s) frequency Intensity: Movement of the hyoid bone without intolerable pain∙ Displacement of hyoid boneMagnetic stimulation resulted in 10.9±2.8 mm forward displacement and 8.3±4.1 mm upward displacement of the hyoid bone.
Kanat et al., 2013TurkeyRCTHand osteoarthritis n=50 Female, 100% Age: PEMF: 64±13 years Sham: 62±12 yearsPain and muscle dysfunctionHandPEMF 25 Hz frequency Intensity: 5–80 G 10 days 20 min/day∙ Handgrip strength ∙ Pinch grip strength ∙ Duruöz Hand OA Index ∙ AUSCAN Hand OA IndexThe significant improvement was observed in Duruöz and Auscan Hand Osteoarthritis Indexes.
Kandemir et al., 2024TurkeyRCTSubacromial impingement syndrome n=80 Female, 61.3% Age: PEMF 49.82±8.05 years Sham 49.62±9.40 yearsSubacromial impingement syndromeShoulderPEMF 50 Hz frequency 85 Gauss intensity 30 min/day 5 days/week 4 weeks∙ ROM (flexion, abduction, internal and external rotation) ∙ Muscle strength (internal and external rotation) ∙ Functional capacity (CMS, SPADI)In the comparison between the PEMF and sham groups, more improvement was found in the PEMF group in active flexion, abduction ROM, and most parameters of functional capacity. No statistically significant difference was found between the groups in muscle strength.
Karakaş and Gök, 2020TurkeyRCTChronic non-specific neck pain n=63 Female, 76.2% Age: 45.1 (25–59) yearsPain and dysfunctionNeckPEMF 10–100 Hz frequency Intensity: 50% 20 min/session Five times/week 3 weeks∙ NPDSPEMF does not provide further improvement in pain and functionality when applied in addition to conventional physical therapy.
Katz, 2020USACase studyn=2 Female, 50.0% Age: 26 and 47 yearsNABiceps/triceps, calvesHIFEM 20 min/session Two times/week 2 weeks∙ Muscle mass (MRI)Analysis of MRI images showed an average increase in all three muscle groups (biceps muscle mass, triceps muscle mass, and gastrocnemius muscle mass).
Katz and Duncan, 2021USAPre–post, single-arm studyn=20 Female, 67.5% Age: PEMF: 65.6±6.6 years Sham: 64.6±11.5 yearsNAArms, calvesHIFEM 20 min∙ Muscle mass (1, 3, and 6 months)Ultrasound images revealed a significant increase in the muscle mass of all studied muscles (biceps brachii, triceps brachii, and gastrocnemius), with the most noticeable improvement in biceps brachii.
Ke et al., 2022ChinaRCTIntracerebral hemorrhage n=26 Female, 46.2% Age: rPMS: 58 (46.5–63.0) years Sham: 56 (46.5–61.5) yearsMotor paralysisCenter of the axilla and the popliteal fossarPMS 20 Hz frequency On 1 s, off 19 s, 1800 pulses 40%–60% output intensity of stimulator 30 min/day at each stimulation site 10 consecutive days∙ UE-FMA ∙ LE-FMA ∙ MRC scaleStatistically significant differences observed between the rPMS group and sham rPMS group for UE-FMA, LE-FMA, proximal MRC of upper extremity, proximal MRC of lower extremity, and distal MRC scores of lower extremity.
Kim and Nam, 2021KoreaRCTLow back pain n=25 Female, rPMS: 76.9% Control: 66.7% Age: rPMS: 34.93±11.51 years Control: 39±13.11 yearsPain and dysfunctionLow backrPMS∙ Korean ODIIn the rPMS group, significant decrease was observed in the Korean ODI after treatment, and there was significant difference in the Korean ODI compared to the control group. Results suggest that rPMS improves the disability in low back pain patients.
Kinoshita et al., 2020JapanCase seriesStroke n=7 Female, 42.9% Age: 61±17 yearsHemiparesis and gait disturbanceLower limb (gluteus maximus muscle, gluteus medius, hamstring muscle, musculus quadriceps femoris, gastrocnemius, and soleus)rPMS 20 Hz (on: 3 s, off: 27 s) frequency Intensity: 10% above the minimal level that evoked a hip, knee, or ankle movement when the patient was at rest 40 min/day 6 days/week∙ 10MWT ∙ FAC ∙ 6MWT ∙ BBS ∙ Step length, symmetrySignificant improvements in walking speed, gait ability, and balance ability, but no significant effect on endurance capacity or step length.
Krammer et al., 2015New ZealandRCTLow back pain n=40 Female, 50.0% Age: PEME: 35.7 years Placebo: 30.2 yearsPain and dysfunctionLow backPEME 27.12 MHz frequency Intensity: 0.03 mT 4 weeks∙ ODI ∙ PSFSThe group treated with active pulsed electromagnetic energy failed to demonstrate any significant additional improvements in ODI and PSFS.
Krath et al., 2017GermanyRCTLow back pain n=87 Female, 54.0% Age: Intervention: 61.93±10.34 years Control: 59.02±11.2 yearsPain and dysfunctionLow backElectromagnetic transduction therapy 3 Hz frequency Intensity: 80 mT 20 min/session Two sessions/week 8 sessions∙ ODIIn both intervention groups, low back-related pain and the degree of disability decreased significantly at follow-up visits. Combination of electromagnetic transduction therapy and conventional therapy proved significantly superior to conventional therapy alone.
Krewer et al., 2014GermanyRCTStroke n=63 Female, 39.7% Age: rPMS: 55±13 years Sham: 54±13 yearsHemiparesisUpper extremityrPMS 25 Hz frequency Intensity: 10% above the level that evoked a wrist or elbow movement taken at rest 20 min/session Two times/day 2 weeks∙ UE-FMA ∙ BIArm motor function did not significantly change over the study period in either group, whereas rPMS had a positive effect on sensory function.
Krzyżańska et al., 2020PolandNRCTDistal radius fracture n=52 Female, 86.5% Age: PEMF: 58.1±18.2 years Con: 63.6±10.4 yearsCast immobilization caused by fractureHand, wrist, distal forearmPEMF 20–30 Hz frequency 6–10 mT 22 sessions (from seventh treatment, patients received PEMF once a day for 10 days, and then three times a week) 30 min/session 6 weeks∙ ROM ∙ Handgrip strength ∙ DASHPEMF group reported significant changes after 3 and 6 weeks of treatment: greater mobility of upper-limb joints, and reduction in disability of the upper limb.
Külcü and Gül, 2009TurkeyRCTKnee osteoarthritis n=45 Female, 77.8% Age: 63.5±10.2 yearsPain and dysfunctionKneePEMF 2, 100, and 25 Hz frequency consecutively Intensity: 2–10 mT 35 min/session 5 sessions/week 15 sessions 3 weeks∙ WOMACWOMAC functional level score (P=0.003) significantly improved in the PEMF group. There were differences between groups regarding the WOMAC functional level scores (P<0.001) after the treatments.
Laufer et al., 2005IsraelRCTKnee osteoarthritis n=103 Female, 60.2% Age: 73.7±6.6 yearsPain and dysfunctionKneePulsed short wave 110 or 300 Hz frequency Intensity: 1.8 or 18 W 20 min/session Three sessions/week 3 weeks∙ WOMAC ∙ TUG ∙ Timed stair-climbing ∙ Timed stair-descending ∙ 3MWTNo significant differences across time or between groups were observed in any of the other measures.
Lee and Nam, 2021KoreaRCTKnee osteoarthritis n=17 Female, rPMS: 88.9% Control: 100.0% Age: rPMS: 71.3±4.78 years Control: 71.2±3.55 yearsPain and dysfunctionKneerPMS∙ 5TST ∙ WOMACIn both the rPMS group and control groups, significant decrease was observed in the 5TST and WOMAC test after treatment, and there was no significant difference in the 5TST and WOMAC test compared to the control group. Results suggest that rPMS and exercises provides pain relief and improves knee joint function in knee osteoarthritis patients.
Lee et al., 2006KoreaRCTLow back pain n=36 Female, 47.2% Age: PEMT: 75±5 years Placebo: 74±4 yearsLow back painLow backPEMT 5 and 50 Hz frequency Intensity: 1.3–2.1T 15 min/session Three times/week 3 weeks∙ Revised ODIThe mean revised Oswestry disability percentage after 4 weeks was significantly improved from the baseline value in the PEMT group, whereas there were no significant differences in the placebo group.
Lim et al., 2018KoreaRCTAcute low back pain n=26 Female, 53.8% Age: rPMS: 52.50±21.45 years Sham: 51.21±17.98 yearsLow back painMost painful lumbar regionrPMS 20 Hz (on: 5 s, off: 25 s) frequency Intensity: 20% of maximal stimulator output 20 min Ten sessions 2 weeks∙ ODI ∙ RMDQSignificant functional improvement was observed in the real rPMS group compared to that in the sham rPMS group after sessions 5 and 10 based on ODI and after session 5 based on RMDQ.
Lin et al., 2001USAProspective, pre–post, single-arm studySpinal cord injury n=8 Female, 0.0% Age: 51±8 yearsPulmonary dysfunction caused by tetraplegiaLower thoracic spineFMS 20 Hz frequency Intensity: 50%–70% 20 min/session Twice a day Five times/week 4 weeks∙ Maximum expiratory pressure at total lung capacity ∙ Expiratory reserve volume ∙ Forced expiratory flow rate at total lung capacity ∙ Maximum expiratory pressure at functional residual capacity ∙ Forced expiratory flow rate at functional residual capacity ∙ Forced vital capacity ∙ Forced expiratory volumeA 4-week protocol of FMS of the expiratory muscles significantly improves voluntary expiratory muscle strength, indicating that FMS can be a noninvasive therapeutic technology in respiratory muscle training for persons with tetraplegia.
Lisi et al., 2019USARCTLow back pain n=42 Female, PEMF: 52.6% Sham: 60.8% Age: PEMF: 34±13 years Control: 37±15 yearsLow back painLow backPEMF Low frequency (range 1–100 Hz) Intensity: low intensity (nT; 10 −9 ) 30 min/session, Two times/day, every day (first 6 weeks) Once daily, 2–3 days/week (next 6 weeks) 12 weeks∙ ODIPEMF provides preliminary evidence of effectiveness in improving function in patients with non-specific low back pain.
Liu et al., 2013ChinaRCTPostmenopausal osteoporosis n=44 Female, 100% Age: PEMF: 61.7±1.3 Alendronate: 63.1±4.3Reduced mobilityLumber supinePEMF 8 Hz frequency Intensity: 3.82mT (peak) 40 min Six times/week 5 weeks∙ Lower-extremity manual muscle test ∙ BBSThere was no significant treatment difference between the PEMF and alendronate groups in the total lower-extremity manual muscle test and BBS score. These results suggested that a course of PEMF treatment with specific parameters was as effective as alendronate in treating postmenopausal osteoporosis.
Massé-Alarie et al., 2013CanadaRCTLow back pain n=13 Female, 61.5% Age: rPMS: 53.6±5.5 years Sham: 53.8±9.8 yearsPostural adjustment disabilityTransversus abdominis/internal oblique musclerPMS 50 Hz frequency Intensity: 33% of maximal stimulator output 10 min One session∙ Quebec Back Pain Disability ScaleTwo weeks after experiment, Quebec Back Pain Disability Scale scores (functional disability) was improved in rPMS group, whereas it was unchanged in sham group.
Massé-Alarie et al., 2017CanadaRCTChronic low back pain n=21 Female, 47.6% Age: rPMS: 33.2±10.8 years Sham: 42.1±17.2 yearsLow back painSuperficial multifidus muscle (L4–L5 level)rPMS 20 Hz (30 contractions of 10 s with 30 s off) frequency Intensity: 35% and 40% of maximal stimulator output 20 min Three times/week 1 week∙ ODI ∙ PSFSrPMS significantly improved the ODI and PSFS.
Moldovan et al., 2012RomaniaRCTKnee osteoarthritis n=65 Female, 72.3% Age: PEMF: 57.7±8.67 years Placebo: 57.8±8.67 yearsPain and dysfunctionKneePEMF 1.5 Hz frequency Intensity: 30 mT 15 min/session 10 days∙ WOMACThere was a significant improvement in WOMAC score in both groups. There was no overall statistically significant difference in the active versus placebo group. In a subgroup analysis, after having excluded the advanced knee osteoarthritis patients with Kellgren-Lawrence scores of 3 and 4, the patients treated with PEMF had superior improvement in WOMAC score.
Momosaki et al., 2014JapanRCTStroke n=20 Female, 30% Age: FMS: 61±22 years Sham: 66±9 yearsPost-stroke dysphagiaSuprahyoid musclesFMS 30 Hz frequency (on: 2 s, off: 28 s) Intensity: 90% of minimal intensity at which patient subjectively feels local pain 10 min One session Single day∙ Timed water swallow test ∙ Interswallow interval ∙ Swallowing volume velocity ∙ Volume per swallowThe improvement of speed and capacity of swallowing after stimulation was significantly larger in the real group than in the sham group. However, no significant difference in the interswallow interval was found between the groups.
Momosaki et al., 2015JapanCase seriesPost-stroke n=8 Female, 25.0% Age: 62–27 yearsDysphagiaSuprahyoid musclesrPMS 20 Hz (on: 3 s, off: 27 s) frequency Intensity: 90% of maximal intensity 10 min Twice daily Six consecutive days∙ Laryngeal elevation delay time ∙ Penetration aspiration scale ∙ Functional Oral Intake Scale ∙ Mann Assessment of Swallowing AbilityrPMS induced significant improvement in swallowing ability, laryngeal elevation delay time, and penetration aspiration scale, but had no significant effect on the functional oral intake scale.
Moretti et al., 2012ItalyRCTTotal knee arthroplasty n=30 Female, NA Age: PEMF: 70.0±10.6 years Control: 70.5±8.1 yearsPain, joint swelling, and physical dysfunctionKneePEMF 75 Hz frequency Intensity: 1.5mT 4 h/day 60 days∙ Knee Society ScoreThe Knee Score demonstrated significantly positive outcomes in the PEMF group compared with the controls at follow-ups. The effect of PEMF therapy was maintained after use of the device was discontinued.
Musarò et al., 2019ItalyRCTALS n=22 Female, 13.6% Age: 61.27±13.44 yearsMuscle dysfunctionArmNeuromuscular magnetic stimulation 5 Hz frequency Intensity: 100% 5 days/week 2 weeks∙ MRC score ∙ Handgrip strength ∙ Muscle fiber type composition, muscle atrophy and wastingA significant effect of neuromuscular magnetic stimulation was observed on MRC scale at the flexor carpi radialis muscle. The improvement observed in neuromuscular magnetic stimulation-treated muscles was associated with counteracting muscle atrophy and down-modulating the proteolysis.
Nagashima et al., 2021JapanPre–post, single-arm studyHealthy adults n=20 Female, 25.0% Age: 32±9 yearsNASuprahyoid musclesElectromyography (EMG)-triggered peripheral magnetic stimulation 30 Hz frequency 2 s when EMG level in sternohyoid muscle exceeded threshold∙ Movement time of hyoid bone ∙ Anterior maximum movement distance of hyoid bone ∙ Opening width of UES ∙ Anterior movement distance of hyoid bone at maximum UES opening ∙ Maximum pressure immediately after UES closureMagnetic stimulation significantly extended the movement time of the hyoid bone. During liquid deglutition, significant increases were observed in the anterior maximum movement distance of the hyoid bone, opening width of the UES, and anterior movement distance of the hyoid bone at the maximum UES opening. In pressure topography, the maximum pressure immediately after UES closure significantly decreased with magnetic stimulation. EMG-triggered peripheral magnetic stimulation made it possible to apply magnetic stimulation during voluntary swallowing.
Nicolakis et al., 2002AustriaRCTKnee osteoarthritis n=32 Female, 59.4% Age: PMF: 69±5 years Sham: 67±7 yearsDisabilityWhole bodyPMF 1–3000 Hz frequency Intensity: 40µT 30 min/session Two times/day 6 weeks∙ WOMAC ∙ Gait speed ∙ Knee extension muscle strengthAfter 6 weeks of treatment, the WOMAC Osteoarthritis Index was more reduced in the pulsed magnetic field group than the sham group. The following secondary parameters improved in the pulsed magnetic field group more than they did in the sham group: gait speed at fast walking, acceleration time in the isokinetic dynamometry strength tests.
Obayashi and Takahashi, 2020JapanNRCTStroke n=19 Female, 31.6% Age: rPMS: 64.3±13.1 years Standard care: 72.3±10.7 yearsSevere upper-limb paresisUpper limb (extensor digitorum communis, extensor carpi radialis, flexor digitorum superficialis, triceps brachii, biceps brachii, and anterior or middle head of deltoid)rPMS 30 Hz (on: 2 s, off: 2 s) frequency Intensity: 70% maximal stimulator output, corresponding to 0.65 T 15–20 min/day 3 days/week∙ UE-FMA ∙ WFMT ∙ BBTSignificant improvement in FMA-UE and WMFT, but not in BBT.
Ogawa et al., 2020JapanRCTHealthy adults n=24 Female, NA Age: Magnetic stimulation: 30±6 years Head lift: 29±5 yearsDysphagiaSuprahyoid musclesrPMS 30 Hz (on: 2 s, off: 8 s) frequency Intensity: 70% of maximum (approximately 0.7 T) 90 times daily 2 weeks∙ Cervical flexor strength ∙ Jaw-opening force ∙ Tongue pressure ∙ Muscle fatigue of the hyoid and laryngeal muscles ∙ Displacement of hyoid bone ∙ Opening width of UESCervical flexor strength significantly increased solely in the magnetic stimulation. Tongue pressure significantly improved in both groups. There were no significant differences in the jaw-opening force, median frequency rate of the anterior belly of the digastric muscle, sternohyoid muscle, sternocleidomastoid muscle, anterior and superior hyoid bone displacement, and UES opening width in both groups.
Oke and Umebese, 2013NigeriaRCTBack pain n=16 Female, 43.8% Age: 42.82±8.63 yearsBack painBackPEMF Four times/day 2 h (total) During admission (8.25±1.83 times)∙ Functional activity scoresThere was a statistically significant faster resumption of active functions in patients treated with PEMF plus analgesic compared with the rates exhibited by patients treated with standard analgesics alone.
Omar et al., 2012EgyptRCTDiscogenic lumbar radiculopathy n=40 Female, 72.5% Age: PEMF: 37.5±8.5 years Sham: 40.0±8.3 yearsLow back pain with radicular symptomsLow backPEMF 7 Hz–4kHz frequency Intensity: 5–15G 20 min daily 3 weeks∙ ODISignificant differences were observed between both groups before and after application of PEMF therapy relative to total ODI (P<0.001), and other domains of ODI.
Özgüçlü et al., 2010TurkeyRCTKnee osteoarthritis n=40 Female, 72.5% Age: PEMF: 60.55±7.7 years Sham: 62.15±8.15 yearsPain and dysfunctionKneePEMF 50 Hz frequency Intensity: 30 G 30 min/session Ten sessions 2 weeks∙ WOMACBoth PEMF and sham PEMF treatment groups showed statistically significant improvement in WOMAC pain and functional scores at the end of treatment. There were no statistically significant differences between groups in WOMAC pain, stiffness, and physical function scores after treatment.
Paolucci et al., 2016ItalyRCTFibromyalgia n=33 Female, 100.0% Age: 50.33±10.94 yearsPainDorsal bodyLow-frequency magnetic field 1–80 Hz frequency Intensity: 100 μT 30 min/session Three times/week 4 weeks∙ FIQ ∙ HAQShort-term benefits of low-frequency magnetic field were observed in FIQ and HAQ scores, with less significant effects seen in the medium term.
Park et al., 2014KoreaRCTLumbar myalgia n=38 Female, 71.1% Age: 31.95±12.3 yearsPain and dysfunctionLow backPEMF 8.56 kHz frequency Intensity: 820 mT 10 min/session Three sessions/week 2 weeks∙ ODI ∙ RMDQPEMF and sham group showed significant improvements in ODI and RMDQ scores. However, RMDQ scores of the PEMF group were much lower than those of the sham group. The two groups showed no significant difference in ODI.
Piatkowski et al., 2009GermanyRCTMultiple sclerosis n=37 Female, Treatment: 89.5% Placebo: 72% Age: Treatment: 44±8.3 years Placebo: 61±8 yearsFatigue-associated physical dysfunctionWhole bodyBio-electro-magnetic-energy-regulation Low frequency Intensity: 14µT 8 min/session Twice everyday 12 weeks∙ Multiple Sclerosis Functional Scale ∙ Expanded Disability Status ScaleThere was a significant difference of Multiple Sclerosis Functional Scale value after 12 weeks in favor of the treatment group.
Pipitone and Scott, 2001UKRCTKnee osteoarthritis n=69 Female, PEMF: 35.3% Control: 20.0% Age: PEMF: 62 (40–84) years Control: 64 (48–84) yearsPain and dysfunctionKneePEMF 3 and 7.8 Hz frequency Intensity: <0.5 G 10 min/session Three times/day 6 weeks∙ WOMACPEMF is beneficial for disability in patients with knee OA resistant to conventional treatment.
Provencher et al., 2022CanadaCase studyCerebral palsy n=1 Female Age: 30 yearsBalance dysfunction, inadequate protective reactions and postural adjustments, inadequate motor control and trunk stabilizationTibialis anterior, deep trunk muscles, hamstringrPMS Four sessions One session/week Tibialis anterior and deep trunk muscles: 2 s on, 8 s off, total of 600 pulses over 200 s Hamstring: 42% maximal stimulator output, total of 600 pulses over 40 s∙ Active ROM (ankle dorsiflexion) ∙ Gait patternActive ankle dorsiflexion was significantly increased. The improvement of ankle function was carried over to the quality of locomotor patterns.
Richards et al., 1997USARCTMultiple sclerosis n=30 Female, 70.0% Age: NAPhysical dysfunctionShoulder, back, or hipPEMF 4–13 Hz frequency Intensity: 50–100mG 10–24 h/day 2 months∙ Extended Disability Status ScaleNo change on the Extended Disability Status Scale, but a significant improvement on the combined mobility performance scale.
Silantyeva et al., 2021RussiaRetrospective, comparative studyParous women n=95 Female, 100.0% Age: HIFEM: 31.1±5.4 years Electrostimulation: 32.0±7.7 years Control: 27.2±4.3 yearsWeakened pelvic floor muscles accompanied by urinary incontinencePelvic areaHIFEM 2.5 T Two or three times/week Ten sessions∙ Pelvic floor integrity (anteroposterior diameter and laterolateral diameter of levator hiatus and hiatal area, and levator–urethra gap) ∙ PFDI-20Three-dimensional ultrasound showed positive changes in pelvic floor dynamics after treatment (decreased anteroposterior diameter, laterolateral diameter, and hiatal area). Significant changes in pelvic floor integrity were observed. A greater degree of improvement in the Pelvic Floor Disability Index questionnaire 20 was observed compared to electrostimulation. Significantly fewer patients in the HIFEM group reported urinary leakage after treatment.
Sorrell et al., 2018USARCTLumbar surgery n=36 Female, 42-μs: 38.4% 38-μs: 50.0% Sham: 64.2% Age: 42-μs: 56.0±14.3 years 38-μs: 51.2±12.3 years Sham: 50.6±12.2 yearsChronic postoperative painBackPEMF 27.12 MHz frequency Intensity: 591±44 V/m 30 min/session Twice daily 60 days∙ ODIODI results were consistent with an overall beneficial effect of the PEMF 42-μs pulse width device.
Sutbeyaz et al., 2006TurkeyRCTCervical osteoarthritis n=32 Female, 65.6% Age: PEMF: 43.15±10.31 years Sham: 42.10±10.12 yearsPain and dysfunctionWhole bodyPEMF 0.1–64 Hz frequency Intensity: 40 µT 30 min/session Two times/day 3 weeks∙ NPDS ∙ Active ROMThe active ROM, paravertebral and neck pain and disability scale scores improved significantly after PEMF therapy, but no change was observed in the sham group.
Taradaj et al., 2018PolandRCTLow back pain n=106 Female, 66.0% Age: Group A (magnetic therapy): 50.45±10.11 years Group B (magnetic therapy): 55.20±11.40 years Group C (placebo magnetic therapy): 52.30±8.22 years Group D (magnetic stimulation): 51.80±11.50 years Group E (placebo magnetic stimulation): 55.75±9.28 yearsLow back painLumbosacral regionMagnetic therapy (Group A) 50 Hz frequency 10 mT 20 min 3 weeks Magnetic therapy (Group B) 50 Hz frequency 5 mT 20 min 3 weeks Magnetic stimulation 195 Hz frequency 49.2 μT 20 min 3 weeks∙ Hip ROM ∙ ODI ∙ RMDQAll comparison groups demonstrated statistically significant improvements in ROM and functional ability. Application of magnetic therapy (Group A: 10 mT, 50 Hz, 20 min) leads to an improvement of functional ability in patients with low back pain.
Thamsborg et al., 2005DenmarkRCTKnee osteoarthritis n=83 Female, 54.2% Age: PEMF: 60.4±8.7 years Sham: 59.6±8.6 yearsPain and dysfunctionKneePEMF 50 Hz frequency Intensity: 50 V 120 min/session 5 days/week 6 weeks∙ WOMACWithin group analysis revealed a significant improvement in ADL, stiffness, and pain in the PEMF-treated group at all evaluations. In the control group, there was no effect on ADL after 2 weeks and a weak significance was seen after 6 and 12 weeks. Significant effects were seen on pain at all evaluations and on stiffness after 6 and 12 weeks. Between group analysis did not reveal significant improvements over time.
Trock et al., 1993USARCTOsteoarthritis (knee, hand, ankle) n=27 Female, NA Age: NAPain and dysfunctionSymptomatic joints (knee, hand, ankle)PEMF 30 Hz frequency Intensity: 10–20 G 30 min/session 3–5 sessions/week 18 sessions 1 month∙ ADL (scale of 1 to 5)An average improvement of 23%–61% occurred in the clinical variables observed with active treatment.
Vadalà et al., 2018ItalyRetrospective, observational, single-arm studyUrinary incontinence n=20 Female, 50.0% Age: 64.14±13.61 yearsUrinary incontinencePelvic floorFMS 10, 35 Hz frequency Intensity: 15%–30% of maximum 20 min/session Two sessions/week 3 weeks∙ Maximum urethral closure pressureUrodynamic tests recorded a significant increase in maximum urethral closure pressure compared with the baseline values.
Venugobal et al., 2023SingaporeRetrospective, single-arm studyOlder adults (voluntary subjects) n=101 Female, 62% Age: 38–91 yearsNAQuadricepsPEMF 1 mT 10 min/day One session/week 12 weeks∙ TUG ∙ 5TST ∙ 4-m normal gait speed ∙ Body composition (weight, skeletal muscle mass, body fat mass, and visceral fat area)Weekly PEMF exposure was associated with significant improvements in mobility (TUG, 5TST, 4-m normal gait speed) and body composition (increased skeletal muscle mass and reduced total and visceral fat mass), particularly in the older participants.
Werner et al., 2016GermanyCrossover designStroke or traumatic brain injury n=40 Female, 40.0% Age: rPMS→Sham: 47.9±8.5 years Sham→rPMS: 55.4±8.6 yearsHemiparesis- or tetraparesis-related dysfunctionForearmrPMS 5 Hz frequency Intensity: not reported 5 min Single session∙ Passive ROMThe mean relative extension deficit of the wrist and MCP joints to neutral showed larger decrease of the relative extension deficit following rPMS as compared to sham.
Wuschech et al., 2015GermanyRCTKnee osteoarthritis n=57 Female, 35.1% Age: 61.1±12.0 yearsKnee painKneePEMF 4–12 Hz frequency Intensity: 105 mT 5 min Two times/day 18 days∙ WOMACTreatment with PEMF showed a highly significant reduction in disability in daily activities according to the WOMAC scales.
Xu et al., 2023ChinaRCTPostpartum pelvic floor dysfunction n=100 Female, 100.0% Age: Intervention: 29.52±3.35 years Control: 29.61±3.43 yearsPostpartum pelvic floor dysfunctionPerineumMagnetic wave 15–50 Hz frequency Intensity: patient’s tolerance and bellows movement of both legs 20 min/session Once every 2 days 8 weeks∙ Pelvic floor muscle strength ∙ PFDI-20Extracorporeal magnetic wave pelvic floor therapy combined with pelvic floor muscle training can effectively improve the clinical efficacy of postpartum pelvic floor dysfunction patients, and improve pelvic floor muscle strength, which has a high clinical reference value.
de Carvalho et al., 2012ItalyCrossover RCTMultiple sclerosis n=50 Female, 70.0% Age: 52.3±10.7 yearsFatigue-associated physical dysfunctionWhole bodyPEMF 4–7 Hz frequency Intensity: 37.5µT 24 min/session Three times/week 8 weeks∙ 10MWTStatistical analysis did not show any significant differences for 10MWT.
Özdemir et al., 2021TurkeyRCTSupraspinatus tendon tear n=40 Female, 67.5% Age: PEMF: 65.6±6.6 years Sham: 64.6±11.5 yearsSupraspinatus tendon tearShoulderPEMF 50 Hz frequency 25 G intensity 25 min/session∙ UCLA Shoulder Scale ∙ SPADINo significant difference was found between PEMF and sham groups according to the UCLA Shoulder Scale and SPADI scores.
Üzelpasaci et al., 2023TurkeyCase reportAnal canal injury n=1 Male Age: 23 yearsFecal incontinencePerianal regionExtracorporeal magnetic innervation 10, 50 Hz frequency Intensity: maximum level 20 min/session Three times/week 10 weeks∙ Pelvic floor muscle strength and endurancePelvic floor muscle exercises and extracorporeal magnetic innervation are effective treatments for increasing the pelvic floor muscle strength and endurance in a patient with colostomy during the preclosure and postclosure periods.
Fig. 2. Distribution of studies by country.
Fig. 2. Distribution of studies by country.

Diseases or Populations and Functional Impairments Treated with PMS

The most common musculoskeletal disease treated with PMS was knee osteoarthritis-related dysfunction (18 studies), 23 , 38 , 39 , 41 , 42 , 46 , 52 , 54 , 68 , 102 , 103 , 105 , 106 , 107 , 108 , 110 , 113 , 116 ) followed by low back pain-related dysfunction (16 studies), 17 , 47 , 48 , 74 , 77 , 80 , 81 , 82 , 83 , 90 , 94 , 96 , 98 , 99 , 101 , 112 ) shoulder impingement syndrome-related dysfunction (3 studies), 29 , 104 , 109 ) and complex regional pain syndrome (2 studies). 35 , 58 ) Other diseases are detailed in Figs. 3 and 4 and Table 5 . 18 , 30 , 31 , 32 , 33 , 37 , 40 , 51 , 59 , 60 , 88 , 92 ) The most common neurological disease treated with PMS was stroke-related dysfunction, including paralysis and dysphagia (16 studies), 22 , 63 , 64 , 65 , 67 , 72 , 73 , 76 , 78 , 84 , 85 , 87 , 89 , 91 , 93 , 95 ) followed by motor impairment caused by cerebral palsy (4 studies), 70 , 71 , 75 , 79 ) multiple sclerosis-related physical dysfunction (3 studies), 50 , 57 , 69 ) spinal cord injury (1 study), 49 ) and amyotrophic lateral sclerosis (1 study). 19 ) In addition, two studies showed that PMS effectively treated COPD-related muscle dysfunction. 15 , 16 ) Incontinence-related diseases treated with PMS included urinary incontinence (6 studies), 36 , 43 , 61 , 97 , 100 , 111 ) antepartum and postpartum incontinence (3 studies), 20 , 53 , 114 ) and anal canal injury (1 study). 34 ) Other applications of PMS included treatment of limb and suprahyoid muscle groups in healthy individuals, 21 , 55 , 62 , 66 , 115 ) skeletal muscles in the elderly, 44 , 45 ) and conditions associated with low bone mineral density and osteoporosis ( Figs. 3 and 4 and Table 5 ). 56 , 86 )

Fig. 3. Types of diseases or populations treated with PMS.
Fig. 3. Types of diseases or populations treated with PMS.
Fig. 4. Types of impairments treated with PMS.
Fig. 4. Types of impairments treated with PMS.

Treatment Site for PMS

The treatment sites for PMS in musculoskeletal diseases included the knee (17 studies), 23 , 38 , 39 , 41 , 42 , 46 , 52 , 54 , 68 , 102 , 103 , 105 , 106 , 108 , 110 , 113 , 116 ) lower back (16 studies), 17 , 47 , 48 , 74 , 77 , 80 , 81 , 82 , 83 , 90 , 94 , 96 , 98 , 99 , 101 , 112 ) shoulder (4 studies), 29 , 30 , 104 , 109 ) and other sites throughout the body (12 studies). 18 , 31 , 32 , 33 , 37 , 40 , 51 , 59 , 60 , 88 , 92 , 107 ) In neurological diseases, PMS was applied to the upper limb in five studies 19 , 65 , 72 , 87 , 89 ) ; the whole body, 57 , 69 ) suprahyoid muscles, 22 , 67 ) shoulder, 63 , 91 ) gluteal muscles, 70 , 71 ) and pelvic girdle 93 , 95 ) in two studies each; and other parts of the body. 49 , 50 , 64 , 73 , 75 , 76 , 78 , 79 , 84 , 85 ) PMS was applied to the quadriceps muscle (2 studies) for respiratory diseases, 15 , 16 ) and pelvic floor muscle (10 studies) for incontinence-related diseases. 20 , 34 , 36 , 43 , 53 , 61 , 97 , 100 , 111 , 114 ) In addition, PMS was applied to the suprahyoid muscle, whole body, and the arms and calves in several other studies ( Fig. 5 and Table 5 ). 21 , 44 , 45 , 55 , 56 , 62 , 66 , 86 , 115 )

Fig. 5. Treatment sites for PMS.
Fig. 5. Treatment sites for PMS.

Treatment Outcomes with PMS

For musculoskeletal diseases, the primary outcome measures for PMS were the Oswestry Disability Index (ODI) 17 , 33 , 47 , 48 , 74 , 77 , 81 , 82 , 83 , 90 , 94 , 96 , 99 , 101 ) and the Western Ontario MacMaster University Osteoarthritis Index (WOMAC), 23 , 39 , 41 , 42 , 46 , 52 , 54 , 68 , 102 , 106 , 107 , 108 , 110 , 113 ) each reported in 14 studies. Range of motion (ROM) was assessed in nine studies 29 , 38 , 40 , 90 , 92 , 94 , 103 , 109 , 116 ) and muscle strength in five. 18 , 29 , 103 , 104 , 107 ) For neurological diseases, the upper-extremity Fugl–Meyer Assessment (UE-FMA) was used in eight studies, 63 , 65 , 72 , 84 , 85 , 87 , 89 , 91 ) ROM in seven, 63 , 73 , 75 , 76 , 78 , 79 , 89 ) gait speed 57 , 64 , 70 ) and Barthel Index 72 , 93 , 95 ) in three each, and muscle strength in two studies. 76 , 78 ) For respiratory disease, the 6-min walk test (6MWT) and fat-free mass index were used to evaluate PMS effects across two studies. 15 , 16 ) For incontinence-related disease, pelvic floor muscle strength was commonly measured. 20 , 34 , 36 , 43 , 53 , 61 , 97 , 100 , 111 , 114 ) Detailed outcome measures for the various diseases and conditions are presented in Fig. 6 and Table 5 .

Fig. 6. Outcomes of the treatment with PMS.
Fig. 6. Outcomes of the treatment with PMS.

Treatment Characteristics for PMS

Study settings are detailed in Table 5 . Treatment intensities varied based on the devices used. Frequencies ranged from 0.06 Hz to 27.12 MHz, session durations spanned 5 min to 12 h, and session frequencies ranged from weekly to daily, with follow-ups extending to 1 year.

Summary and Synthesis of the Impact of PMS on Commonly Treated Diseases

For knee osteoarthritis, improvements were observed in the WOMAC and ROM. For low back pain, improvements were noted in the ODI and Roland–Morris Disability Questionnaire (RMDQ). For stroke, improvements were observed in UE-FMA, ROM, muscle strength, gait parameters, and ADL. For COPD, improvements were observed in 6MWT, and increased pelvic floor muscle strength was reported for incontinence-related conditions. PMS improved pain-related impairments in musculoskeletal disorders and upper limb function following stroke. Studies on respiratory and incontinence-related disorders were limited and heterogeneous, although some demonstrated improvements in exercise capacity and pelvic floor muscle strength ( Table 6 ).

Table 6.
Summary of the impact of PMS on commonly treated diseases

DiseaseMain treatment siteSummary of PMS settingsMajor evaluation outcomesSummary of results
Knee osteoarthritisKneeFrequency: 0.06–3000 Hz Stimulation session: 10 min–12 h Duration: 9 days–26 weeksWOMACImprovement (no significant difference between groups, superior improvement in subgroup analysis)
ROMImprovement (no significant difference between groups)
Low back painLow backFrequency: 3 Hz–27.12 MHz Stimulation session: one session–20 min Duration: 1 day–12 weeksODIImprovement (no significant difference between groups)
RMDQImprovement (possibly superior to placebo)
StrokeVarious sitesFrequency: 5–40 Hz Stimulation session: one session–40 min Duration: 1 day–8 weeksUE-FMAImprovement (significant improvement compared to controls)
ROMImprovement (significant improvement compared to placebo)
Muscle strengthImprovement (significant improvement compared to placebo)
GaitImprovement (significant improvement in gait speed, gait ability, and balance ability. No significant effects on endurance capacity or step length)
ADLImprovement (possibly superior to controls)
COPDQuadriceps muscleFrequency: 8–15 Hz Stimulation session: 15 min Duration: 3–8 weeks6MWTImprovement (no group comparison)
Incontinence-related diseasePelvic floor muscleFrequency: 5–50 Hz Stimulation session: 20–30 min Duration: 3–8 weeksPelvic floor muscle strengthImprovement (no significant difference between groups)

DISCUSSION

In this scoping review, we aimed to identify, summarize, and map the relevant literature on the current use of PMS for various diseases and related dysfunctions, while also highlighting areas for future research. Notably, no previous studies have explored the application of PMS across domains with a specific focus on functional impairment, making this review both novel and original.

Our findings indicate an increasing use of PMS for various conditions. Many studies using PMS were conducted in Turkey, the United States, Italy, and Japan. Based on disease types and associated functional impairments, we categorized the studies into five areas, including musculoskeletal diseases, neurological diseases, respiratory diseases, incontinence-related diseases, and others. Musculoskeletal diseases accounted for the highest number of studies, especially knee osteoarthritis and low back pain. Interventions targeting pain-related dysfunctions were applied to the affected area, and outcomes were commonly assessed using disease-specific measures (such as WOMAC, ODI, and RMDQ), along with evaluations of ROM and muscle strength. Neurological diseases were the second most frequently studied category, with stroke being the most common. In particular, PMS was often applied to upper-limb paralysis, with UE-FMA, ROM, muscle strength, gait parameters, and ADL serving as key outcome measures.

The mechanisms of action for PMS treatment can be broadly categorized as neuromodulation of central and peripheral pathways, alteration of cortical excitability and plasticity, and direct muscular and neural activation. 117 , 118 , 119 ) In addition, growing preclinical and in vitro evidence suggests that PMS modulates inflammatory cytokines and promotes the release of growth factors, 120 , 121 ) thereby facilitating neural repair, muscle regeneration, and anti-inflammatory effect. Musculoskeletal diseases are most commonly associated with pain and pain-related disabilities. 122 ) The aforementioned neuromodulation of central and peripheral pathways, alterations in cortical excitability and plasticity, direct muscle and nerve activation, and suppression of inflammatory cytokines potentially reduce pain, 117 , 118 , 119 , 120 , 121 ) which in turn is associated with improved physical function. 10 , 11 ) Furthermore, although the detailed mechanism remains unclear, PMS reportedly affects physical function in knee osteoarthritis without improvement in pain, 123 ) thus supporting its effect on physical function. In stroke survivors, PMS may optimize neuromuscular activity at the treatment site, strengthen synaptic connections within the spinal cord, activate the cerebral cortex via afferent input, and regulate corticospinal motor excitability. 85 , 124 ) In the early post-stroke stage, spontaneous recovery comprises synaptogenesis, dendritic and axonal sprouting, and migration of neural stem cells. 125 , 126 ) PMS application during this period may facilitate a coupling effect between cortical reorganization and neural regeneration, potentially improving upper limb function, physical function, and ADLs. PMS has also been applied to strengthen pelvic floor muscles and prevent incontinence-related diseases. This review confirmed that improvements in pelvic floor muscle function are attributable to an underlying mechanism where changing magnetic fields stimulate pelvic floor nerves, causing repetitive contractions. 127 ) PMS offers advantages over electrical stimulation therapy because it is non-invasive and allows treatment while individuals remain fully clothed. 123 ) In COPD, PMS has been applied to the quadricep muscles, with exercise capacity serving as the main outcome measure. Although limited in number, studies suggest that PMS may improve exercise capacity, potentially by improving muscle function. 15 , 16 )

Regarding representative musculoskeletal diseases of knee osteoarthritis and low back pain, although significant differences between the intervention and control groups were not always confirmed, our findings revealed that PMS improves functional aspects ( Table 6 ). Regarding neurological diseases, consistent benefits were identified in post-stroke upper limb paresis, ROM, muscle strength, gait, and ADLs. Regarding incontinence-related disease, significant differences observed between both groups were less consistent, and the number of studies was limited; however, a trend toward improvement with the intervention was noted. Regarding COPD, within-group comparisons showed improvements in exercise tolerance; however, no studies conducted between-group comparisons. Based on current evidence, PMS should be prioritized for treating neurological and musculoskeletal diseases, including knee osteoarthritis and low back pain, because multiple trials have demonstrated benefits in these conditions. Although clinically recommended practices exist for incontinence-related diseases, supporting evidence remains inconsistent. Conversely, evidence for its use in COPD, a common respiratory disease, remains limited. Furthermore, no reports exist on the use of PMS for other internal diseases, such as cardiovascular disease, cancer, or diabetes mellitus. In other words, the impacts of PMS on these conditions remain unclear, and efforts to address the functional impairments associated with these conditions 124 , 125 , 126 , 127 ) must begin with the verification of safety and mechanisms of action. The characteristics of PMS treatment varied across diseases and dysfunctions; PMS was also provided in various settings, even for the same conditions. These variations are likely attributable to differences in the intensity and frequency of PMS in different settings. In the future, identifying effective applications of using PMS for specific diseases and dysfunctions and establishing standard PMS prescriptions are essential.

This review had some limitations. First, despite the acquisition of a substantial amount of information, the risk of bias was not evaluated. Although risk-of-bias assessments are not mandatory for scoping reviews, evaluating the quality of the included studies could reveal new issues and lead to different conclusions. Second, because this was a scoping review without a quantitative synthesis, publication bias was not formally assessed. However, given that grey literature was excluded, the findings may be influenced by the selective publication of positive results. Third, this study focused exclusively on English-language articles, and studies published in other languages were not included; therefore, some relevant studies may have been missed. Fourth, owing to the variability in PMS device settings across studies, we could not examine the effects of stimulation parameters. Fifth, because the intervention duration varied among studies, we could not verify the optimal duration of the effect. These issues need to be addressed in the future.

CONCLUSION

This scoping review clarifies the current applications of PMS across various diseases and related dysfunctions. Based on current evidence, PMS should be prioritized for treating neurological and musculoskeletal diseases, including knee osteoarthritis and low back pain. Although the evidence is inconsistent, there are clinically recommended practices for treating incontinence-related diseases. Conversely, evidence for its use in COPD, a common respiratory disease, remains limited. Furthermore, no studies to date have reported the use of PMS for other internal diseases, such as cardiovascular disease, cancer, or diabetes mellitus. Because the impacts of PMS on these conditions are unclear, efforts to address the associated functional impairments must begin with the verification of its safety and mechanisms of action. In addition, standardized PMS prescriptions have not yet been established. Future studies are warranted to clarify the safety and efficacy mechanisms in areas where PMS has not been implemented and to determine effective PMS settings for each disease.

ACKNOWLEDGMENTS

The authors thank the members of the Faculty of Rehabilitation and Department of Physical Medicine and Rehabilitation, Kansai Medical University, for their support, guidance, and cooperation. This work was supported in part by the Japan Society for the Promotion of Science (grant number 25K00126).

CONFLICTS OF INTEREST: The authors declare no conflict of interest.

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ИП Урсолов Владлен Сергеевич

ИНН 500118482352 · ОГРНИП 314500117700049

Реквизиты и контакты