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Psycho-oncology · 2026

Creative Arts Therapy for Anxiety, Depression, and Quality of Life in Cancer Patients: A Systematic Review and Meta-Analysis of Randomized Controlled Trials.

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Chou ASL, McKechnie T, Arora V, DePestel B, Wang A, Parpia S, Calic G, Staibano P, Derus A, Guleria A, Bhandari M, Thabane A

Аннотация

BackgroundCancer is a significant psychological burden for patients. Previous evidence syntheses suggest creative arts therapies (CATs) may improve psychological outcomes, but are limited by heterogeneity in intervention types, study designs, and outcomes, and the lack of a certainty of evidence assessment.AimsWe conducted a robust systematic review and meta-analysis of current randomized trial literature to explore the efficacy of CATs in improving anxiety, depression, and quality of life in cancer patients.MethodsWe searched PubMed, Embase, and PsycInfo databases for peer-reviewed randomized trials evaluating the effectiveness of CATs against a control in patients with current cancer diagnoses. We performed pairwise random-effects meta-analyses of standardized mean differences (SMD) for anxiety, depression, and quality of life, stratified by time-interval. We conducted subgroup analyses by session frequency, intervention type, treatment setting, and region. For studies not pooled quantitatively, results were qualitatively summarized.Results67 randomized trials with 6259 patients were included. The majority of interventions were music-based (80.6%), multi-session (59.7%), inpatient-based (73.1%), and conducted in North America (29.9%). Meta-analyses demonstrated positive effects of CATs on anxiety at ConclusionCreative arts therapies may improve anxiety, depression, and quality of life among cancer patients.

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This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.

Introduction

The creative arts, which include dance‐movement, drama, film, music, and art [ 1 ], are typically pursued for the purposes of personal expression and enjoyment. But their psychological benefits are well established: engagement in the creative arts has been reported to improve well‐being, enhance life satisfaction, and reduce stress [ 2 , 3 ]. Given such benefits, there has naturally been great interest in the use of the creative arts as a therapeutic intervention.

The use of the creative arts for therapeutic purposes has a long and rich history. The ancient Chinese are known to have used music to treat the sick – in fact, the Chinese character for medicine, yào , is derived from the character for music, yuè [ 4 ]. Similarly, the Egyptians performed the traditional Zar dance for the purposes of healing [ 5 ]. This tradition of using the creative arts for healing persists today through what we now term ‘creative arts therapies’ (CATs). The American Psychological Association (APA) defines CATs as “therapeutic interventions that use artistic endeavors or mediums, such as music, poetry, dance, and drama, to facilitate communication and emotional expression, enhance self‐awareness, and foster health and change.” [ 6 ] CATs have been utilized in a range of patient populations, and to great effect: meta‐analyses have found CATs to significantly improve psychological outcomes for patients with depression [ 7 , 8 ], post‐traumatic stress disorder [ 9 ], and cognitive decline [ 10 , 11 ]. Given the evidence of efficacy in improving outcomes in these populations, CATs have also been trialled in patients with another psychologically taxing condition: cancer.

In more ways than one, cancer is a considerable trial for patients. The strain of such a life‐threatening illness often leads to many experiencing symptoms of psychological distress: anxiety and depression prevalence rates over 20% have been reported [ 12 , 13 ]. These psychological disorders are particularly worrisome as they can reduce adherence to treatment [ 14 ] and even increase the risk of mortality [ 15 ]. Thus, improving the psychological state of cancer patients could have a meaningful impact on prognosis. CATs provide a promising intervention to do so.

Over the last 15 years, substantial research has been conducted on the use of CATs in cancer patients, facilitating in the performance and publication of several systematic reviews and meta‐analyses [ 16 , 17 , 18 , 19 , 20 , 21 , 22 ]. While these evidence syntheses in general suggest a benefit of CATs, the findings across these studies are often conflicting. More, there is substantial heterogeneity across reviews in the types of study designs included and outcomes assessed, and most do not explore any clinically relevant subgroup effects (i.e., frequency of sessions, type of CAT, setting, region), which limits the ability to conclude which types of CATs are most effective for which patients, in which outcomes and settings. Thus, there is a clear need for a new meta‐analytic synthesis of the literature, particularly one focused on randomized controlled trials and exploring the differential effectiveness of CATs by session frequency, type of CAT, intervention setting, and region. We conducted the present study to fill this gap. We hypothesize, based on the existing literature [ 17 , 18 ], that CATs will be effective in reducing anxiety and depression and improving quality of life.

Methods

This systematic review and meta‐analysis is reported in accordance with the Preferred Reporting Items for Systematic Reviews and Meta‐Analyses (PRISMA) [ 23 ]. We registered this review on PROSPERO (CRD420251087592). As an analysis of secondary aggregate data, we did not require ethics approval for this study.

Objectives

The primary objective of this systematic review and meta‐analysis was to evaluate the efficacy of CATs in improving anxiety, depression, and quality of life in cancer patients. As secondary objectives, we sought to explore whether there were subgroup effects from the following characteristics: session frequency (single vs. multi‐session), intervention type (art vs. music vs. other types of CAT), treatment setting (inpatient vs. outpatient), and region (continent).

Eligibility Criteria

We considered studies that met the following criteria eligible for this review: (1) Randomized controlled trials; (2) exploring a CAT intervention of any kind (i.e., music, visual art, dance/movement, writing); (3) conducted in adult subjects (i.e., 18 years of age or older) with a current diagnosis of cancer; (4) measured one or more of anxiety, depression, and quality of life; and (5) published in a peer‐reviewed journal. Studies were excluded if they were published as abstracts or conference proceedings, were secondary analyses, included patients in remission from cancer, or were not published in English.

Search Strategy

We searched the MEDLINE, Embase, and PsycInfo databases from inception through February 2025 for eligible articles. We combined Medical Subject Heading (MeSH) terms (e.g., neoplasms, Oncology) and key words (e.g., creative arts therapy, movement therapy, art therapy, music therapy), using the Boolean operators AND/OR. Our search strategy can be found in Supporting Information S1 : Appendix A1.

Study Selection Process

Four reviewers (VA, BD, AC, AW) performed title and abstract screening, and subsequently full‐text review, independently and in duplicate using the Covidence online platform. Any discrepancies were resolved by discussion until consensus, and if necessary, adjudication by the senior author (AT).

Data Collection Process

Similar to the study selection process, a team of three reviewers (AC, VA, BD) performed data extraction independently and in duplicate using a custom data collection form developed using Microsoft Excel. Any discrepancies were resolved by the senior author (AT). Extracted data included study characteristics (i.e., author, year of publication, study design, location of study, number of included centers, study inclusion/exclusion criteria, primary outcomes), patient demographics (e.g., age, sex), disease characteristics (e.g., type of cancer, stage of malignancy), intervention characteristics (e.g., type, number of sessions, duration of treatment), and outcome data at all available time‐points for the outcomes of interest.

Outcomes

The primary outcomes of interest in this review were anxiety, depression, and quality of life. We defined anxiety as an “uncontrollable, diffuse, unpleasant, and persistent state of negative affect, characterized by apprehensive anticipation regarding unpredictable and unavoidable future danger, and accompanied by physiological symptoms of tension and a constant state of heightened vigilance” [ 24 , 25 ]. We defined depression as a mood disorder characterized by sadness, emptiness, or irritable mood, accompanied by somatic and cognitive changes that significantly affect the individual's capacity to function [ 26 ]. We defined quality of life using the World Health Organizations definition of “individual's perception of their position in life in the context of the culture and value systems in which they live and in relation to their goals, expectations, standards and concerns” [ 27 ].

Risk of Bias & Certainty of Evidence

To assess the risk of bias in the included studies, we used the Cochrane Risk of Bias Tool for Randomized Controlled Trials 2.0, which consists of five domains: (1) bias arising from the randomization process, (2) bias due to deviations from intended interventions, (3) bias due to missing outcome data, (4) bias in measurement of the outcome, and (5) bias in selection of the reported result [ 28 ]. Two reviewers (AC, VA) assessed the risk of bias of each study independently and in duplicate, with discrepancies resolved by a third reviewer (AT). For each outcome, the senior author (AT) assessed the certainty of the evidence using the Grading of Recommendations Assessment, Development and Evaluation (GRADE) framework [ 29 ]. We reported the results of the risk of bias and GRADE assessments in tables.

Statistical Analysis

To meet our primary objective, we conducted pairwise, DerSimonian and Laird random‐effects meta‐analyses of standardized mean differences (SMD) for each of the outcomes of interest. To perform these analyses, we utilized mean scores with the associated standard deviation (SD). If standard errors were reported, we converted them to standard deviations by multiplying the value by the square root of the sample size.

As each study reported data at variable time‐points, we stratified the analyses for each outcome into time‐point intervals based on the most frequently reported follow‐up timings across the included studies. This resulted in the following time‐points: immediate (0–6 days post‐intervention), 1–3 weeks post‐intervention, 4–6 weeks post‐intervention, 2–3 months post‐intervention, and 4–6 months post‐intervention. In the case of randomized trials with more than two experimental groups (i.e., CATs), we included the pairwise comparison of both experimental groups with the control group as separate studies (e.g., Arruda 2016a and Arruda 2016b). We assessed the statistical heterogeneity within each meta‐analyses via the I 2 statistic, considering an I 2 greater than 40% to represent substantial heterogeneity [ 30 ]. Finally, where more than 10 studies were included in a meta‐analysis, we assessed the risk of publication bias via visual inspection of a funnel plot. The pooled SMD from each analysis, with the associated 95% confidence interval (95% CI) are reported in forest plots and tables.

To meet our secondary objective, we conducted four exploratory subgroup meta‐analyses for each outcome (and time‐point) based on the following baseline characteristics: intervention type (i.e., art therapy; music therapy; other), session frequency (i.e., single session; multi‐session), setting (i.e., inpatient, outpatient), and region (i.e., North America; South America; East Asia; West Asia; Europe; Africa). The results of the subgroup analyses are presented narratively and in forest plots. Due to the large number of planned subgroup comparisons across multiple outcomes, subgroups, and time‐points, we felt that formal hypothesis testing using p ‐values would substantially increase the risk of false findings and reduce interpretability. We therefore focused on estimation rather than significance testing, with a subgroup considered to show evidence of benefit when the confidence interval of the effect size estimate did not cross zero.

We performed all analyses independently and in duplicate to minimize the risk of human error. The meta‐analyses were conducted in STATA Version 15 (TM) and R Software (version 4.3.2) via RStudio (AT) using the metagen and forest packages.

Qualitative Analysis

For studies that were unable to be included in the meta‐analyses due to lack of reporting of the necessary statistics, we qualitatively analyzed their results to determine whether a significant improvement was observed in each of the three outcomes of interest. We categorized each result in one of three categories: a significant positive benefit with CATs (green label), no significant effect with CATs (gray label), or a significant negative effect with CATs (red label). The results are summarized narratively and reported in a table.

Results

Literature Search

We identified 1168 studies in our database search. After removal of duplicates and title and abstract screening, 166 studies progressed to full‐text review. Upon completion of full text review, we included a total of 67 studies in the systematic review. The full literature search details can be found in Figure 1 .

FIGURE 1 Prisma flow diagram.
FIGURE 1 Prisma flow diagram.

Study Characteristics

The 67 randomized trials, which were published between 2003 and 2024, included a total of 6259 cancer patients. Most were simple, two‐arm parallel randomized trials ( n = 56), with some three‐arm designs ( n = 10), and one four‐arm design. A modest proportion were conducted in the United States ( n = 20), followed by Turkey ( n = 10) and China ( n = 10). Studies most commonly recruited breast cancer patients ( n = 25) or included all types of cancer patients ( n = 18). The most common CAT type studied was music therapy (i.e., music listening or music‐making interventions; n = 54). The majority of interventions were multi‐session ( n = 40) and took place in an inpatient setting ( n = 49). In almost every study, the control group was simply the standard of care ( n = 62); however, one study utilized a sham intervention [ 31 ], one intravenous midazolam [ 32 ], one oral escitalopram [ 33 ], and two meditation [ 34 , 35 ]. Duration of follow‐up ranged from immediately post‐intervention to 12 months post‐intervention. A complete table of study details can be found in Table 1 .

TABLE 1
Study characteristics.
a Median age. b Mean age of all participants from all groups. c Estimated from 2 cycles of chemotherapy. Abbreviations: BAI (C) = Beck Anxiety Inventory (Chinese), BDI = Beck Depression Inventory, CES‐D = Center for Epidemiologic Studies Depression Scale, EORTC‐QLQ‐C30 = European Organisation for Research and Treatment of Cancer Quality of Life Questionnaire Core 30, FACT (G/B) = Functional Assessment of Cancer Therapy (General/Breast), HADS (A/D) = Hospital Anxiety and Depression Scale (Anxiety/Depression), HAMD‐24 = Hamilton Depression Rating Scale 24‐item, HQLI‐R = Hospice Quality of Life Index‐Revised, NVAAS = Numeric Visual Analog Anxiety Scale, PAI (A/D) = Personality Assessment Inventory (Anxiety/Depression), POMS (A/D) = Profile of Mood States (Anxiety/Depression), PROMIS = Patient‐Reported Outcomes Measurement Information System, QMS (A/D) = 12‐item Quick Mood Scale (Anxiety/Depression), QoL = Quality of Life, SAI = State Anxiety Scale, SAS = Zung Self‐Rating Anxiety Scale, SCL‐90‐R (A/D) = Symptom Checklist‐90‐Revised (Anxiety/Depression), SF‐36 = 36‐item Short‐Form Health Survey, STAI (Y/6) = State‐Trait Anxiety Inventory (20‐item/6‐item scale), VAS = Visual Analogue Scale, WHOQOL‐BREF = World Health Organization Quality of Life ‐ Abbreviated, ZSDS = Zung Self‐Rating Depression Scale.

First author Year CountrySettingDesignOutcomesCancerStageArmNMean age (SD)% femaleDuration, # of sessions
Alcântara‐silva 2018 Brazil [ 36 ]Cancer centerParallel groupDepression (BDI), QoL (FACT‐G)Breast or gynecologicalNRMusic therapy5351.85 (10.6)1005+ weeks, 10+ sessions
Control6352.9 (10.26)100
Akbulak 2023 Turkey [ 37 ]Outpatient chemotherapy unitParallel groupAnxiety (STAI)BreastI‐IIIMandala coloring4146.1 (7.7)1001 day, 1 session
Control4350.8 (9.2)100
Alam 2016 United States [ 38 ]HospitalParallel groupAnxiety (STAI)Basal or cutaneous squamous cell carcinoma of the faceNRGuided imagery5062.7 (NR)46.001 day, 1 session
Pre‐recorded music listening5462.4 (NR)40.74
Control5164.2 (NR)39.22
An 2022 China [ 33 ]HospitalParallel groupDepression (HAMD‐24), QoL (QLQ‐C30)AnyNRChaihu plus longgu muli decoction with five‐element music therapy6056.05 (8.73)38.3320 days, 40 sessions
Control (escitalopram 10 mg/d)6055.76 (8.81)41.67
Arruda 2016 Brazil [ 39 ]HospitalParallel groupDepression (BDI)AnyNRPre‐recorded music listening22NR (NR)72.733 days, 3 sessions
Pre‐recorded recited poem listening22NR (NR)72.73
Control21NR (NR)71.43
Bates 2017 United States [ 32 ]HospitalParallel groupAnxiety (POMS‐tension), depression (POMS‐depression)Multiple myeloma or lymphomaNRMusic therapy3758 a (NR)51.356 days, 2 sessions
Control4558 a (NR)40.00
Binns‐turner 2011 United States [ 40 ]HospitalParallel groupAnxiety (SAI)BreastNRPre‐recorded music listening1556.63 b (NR)1001 day, 1 session
Control1556.63 b (NR)100
Bradt 2024 United States [ 41 ]HospitalParallel groupAnxiety (PROMIS anxiety)AnyIII‐IVMusic therapy4557.4 (11.54)73.3312 weeks, 6 sessions
Control (social attention)4754.94 (11.7)70.21
Bro 2019 Denmark [ 42 ]HospitalParallel groupAnxiety (STAI‐Y), QoL (EORTC‐QLQ‐30)Hodgkin or non‐Hodgkin lymphomaNRLive music listening4759 (18)51.06NR, 5 sessions
Pre‐recorded music listening4761 (15)40.43
Control4959 (18)40.82
Bulfone 2009 Italy [ 43 ]HospitalParallel groupAnxiety (STAI‐Y)BreastI‐IIPre‐recorded music listening3049.2 (6.9)1001 day, 1 session
Control3052.7 (6.1)100
Cassileth 2003 United States [ 44 ]Cancer centerParallel groupAnxiety (POMS‐tension), depression (POMS‐depression)HematologicNRMusic therapy3653 (11)38.8910 days, 5 sessions
Control3351 (12)69.70
Chen 2013 Taiwan [ 45 ]HospitalParallel groupAnxiety (STAI)Head and neck, gynecological, breast, digestive tract, lung, or prostateI‐IVPre‐recorded music listening10055.06 (13.5)36.001 day, 1 session
Control10055.66 (11.41)43.00
Chen 2018 Taiwan [ 46 ]Meditation room (group music therapy) or home (self‐directed music therapy)Parallel groupAnxiety (HADS‐A), depression (HADS‐D)BreastNRGroup music therapy20NR (NR)1008 weeks, 8 sessions
Self‐directed music therapy20NR (NR)100
Control20NR (NR)100
Chen 2020 Taiwan [ 47 ]Outpatient chemotherapy unitParallel groupAnxiety (HADS‐A), depression (HADS‐D)Breast0‐IIMusic therapy5051.16 (9.21)1001 day, 1 session
Control5049.56 (9.78)100
Cho 2024 South Korea [ 48 ]HospitalParallel groupAnxiety (STAI)BladderNRPre‐recorded music listening8069.3 (9.7)01 day, 1 session
Control8069.2 (12.6)0
Chuang 2024 Taiwan [ 49 ]HospitalParallel groupAnxiety (STAI), QoL (WHOQOL‐BREF)Breast0‐IVPre‐recorded music listening6352 (10)10012 weeks, 12 sessions
Control6553.2 (9.6)100
Clark 2006 United States [ 50 ]Cancer centerParallel groupAnxiety (HADS‐A), depression (HADS‐D)AnyNRPre‐recorded music listening3558.61 (13.8)37.141 day, 1 session
Control2856.71 (11.0)39.29
Conrad 2016 United States [ 51 ]HospitalParallel groupAnxiety (VAS)BreastNRLive music listening6858.8 (14.4)1001 day, 1 session
Pre‐recorded music listening6858.2 (17.6)100
Control6561.3 (14.9)100
Czamanski‐Cohen 2019 Israel [ 31 ]Cancer centerParallel groupDepression (CES‐D)BreastNRArt therapy4NR (NR)1008 weeks, 8 sessions
Mandala coloring (sham art therapy)5NR (NR)100
Danhauer 2010 United States [ 52 ]Cancer centerParallel groupAnxiety (STAI)HematologicNRPre‐recorded music listening2950.2 (14.1)65.521 day, 1 session
Control3051.6 (13.8)53.33
Deng 2022 China [ 53 ]HospitalParallel groupAnxiety (VAS)BreastNRAromatherapy4054.4 (11.5)1001 day, 1 session
Pre‐recorded music listening4054.2 (9.8)100
Aromatherapy + pre‐recorded music listening4052.4 (12.5)100
Control4050.2 (10.6)100
Du 2024 China [ 54 ]HospitalParallel groupAnxiety (STAI)Non‐small cell lung carcinomaI‐IVMusic therapy3157 (NR)22.581 day, 2 sessions
Control3157 (NR)25.81
Duzgun 2024 Turkey [ 55 ]HospitalParallel groupAnxiety (STAI)Lung, pancreas, gastric, colon, or breastNRMusic therapy30NR (NR)20.00NR, 6 sessions
Control30NR (NR)20.00
Ferrer 2007 United States [ 56 ]Outpatient chemotherapy unitParallel groupAnxiety (VAS)AnyNRLive music listening25NR (NR)NR1 day, 1 session
Control25NR (NR)NR
Firmeza 2017 Brazil [ 57 ]Outpatient clinicParallel groupAnxiety (STAI)Head and neckNRPre‐recorded music listening20NR (NR)NR1 day, 1 session
Control20NR (NR)NR
Gezgin Yazici 2024 Turkey [ 58 ]Outpatient chemotherapy unitParallel groupAnxiety (STAI)AnyNRPre‐recorded music listening3060.13 (10.77)50.004–6 weeks c , 3 sessions
Control3061.07 (13.78)40.00
Giordano 2023 Italy [ 32 ]HospitalParallel groupAnxiety (VAS)Micro‐invasive oral cancerI‐IIMusic therapy3061 (12)93.331 day, 1 session
Control (IV midazolam 0.02 mg/kg)3061 (12)86.67
Hanser 2006 United States [ 59 ]Cancer centerParallel groupAnxiety (HADS‐A), depression (HADS‐D), QoL (FACT‐G)BreastIVMusic therapy3553 a (NR)1009–15 weeks, 3 sessions
Control3550 a (NR)100
He 2022 China [ 60 ]HospitalParallel groupQoL (FACT‐B)BreastI‐IIIDance therapy8847.99 (8.62)10016 weeks, 86 sessions
Control (health consultation)8848.32 (10)100
Hilliard 2003 United States [ 61 ]In‐home hospiceParallel groupQoL (HQLI‐R)AnyNR (terminal)Music therapy4066 (NR)50.00NR, 2‐13 sessions
Control (routine hospice care)4065 (NR)50.00
Ho 2016 Hong Kong [ 62 ]Hospital and community cancer support centerParallel groupAnxiety (HADS‐A), depression (HADS‐D), QoL (FACT‐B)Breast0‐IIIDance therapy6948.6 (7.7)1003 weeks, 6 sessions
Control7049.1 (8.7)100
Jang 2016 South Korea [ 63 ]ClinicParallel groupAnxiety (PAI‐A), depression (PADI‐D), QoL (EORTC‐QLQ‐30)Breast0‐IIIMindfulness‐based art therapy1251.75 (5.32)10012 weeks, 12 sessions
Control1251.42 (6.33)100
Joly 2022 France [ 64 ]HospitalParallel groupQoL (FACT‐G)BreastNRArt therapy12555 (8)1008 weeks, 8 sessions
Control12755 (9)100
Karadag 2019 Turkey [ 65 ]Outpatient radiation oncology clinicParallel groupAnxiety (HADS‐A), depression (HADS‐D)BreastI‐IIPre‐recorded music listening3062.2 (12.49)1005 weeks, 25 sessions
Control3056.6 (13.66)100
Kwekkeboom 2003 United States [ 66 ]Outpatient oncology clinicParallel groupAnxiety (STAI)AnyNRDistraction (listening to book on tape)1455.5 (14.12)85.711 day, 1 session
Pre‐recorded music listening2451.96 (15.21)62.50
Control2053.3 (17.83)65.00
Lazaro‐Garcia 2024 Spain [ 67 ]HospitalParallel groupAnxiety (HADS‐A), depression (HADS‐D), QoL (FACT‐G)Acute myeloid leukemiaNRPre‐recorded music listening4053.01 (NR)45.0019–42 days, 19‐42 sessions
Control3153.89 (NR)41.94
Li 2012 China [ 68 ]HospitalParallel groupAnxiety (STAI)BreastNRPre‐recorded music listening6044.88 (9.37)10051.4 days, ∼100 sessions
Control6045.13 (9.48)100
Liao 2013 China [ 69 ]HospitalParallel groupQoL (HQLI‐R)AnyIVChinese‐medicine five‐element music listening6663.09 (12.46)53.033 weeks, 15 sessions
Western music listening6363.52 (14.65)49.21
Control3162.68 (13.87)54.84
Lima 2020 Brazil [ 34 ]HospitalParallel groupAnxiety (Bai), depression (BDI‐II), QoL (WHOQOL‐BREF)BreastNRPre‐recorded music listening1649.5 (10.65)1004–6 weeks c , 3 sessions
Control (self‐relaxation without music)1750.76 (9.45)100
Lin 2011 Taiwan [ 70 ]Outpatient chemotherapy unitParallel groupAnxiety (Chinese STAI)AnyNRMusic therapy3450.2 (13.5)61.761 day, 1 session
Verbal relaxation3054.3 (9.4)70.00
Control3454.3 (13.6)67.65
McCabe 2013 Ireland [ 71 ]Stem cell transplant centerParallel groupAnxiety/Depression (HADS)HematologicNRArt therapy (Open Window)96NR (NR)39.581+ week, 3+ sessions
Control103NR (NR)41.75
Mollaoglu 2023 Turkey [ 72 ]HospitalParallel groupAnxiety (Bai), QoL (FACT‐G)BreastI‐IIIMarbling + Ney music30NR (NR)1005 weeks, 10 sessions
Control30NR (NR)100
Mondanaro 2021 United States [ 73 ]HospitalParallel groupAnxiety/Depression (HADS)Lung, breast, or gastrointestinalNRMusic therapy4355 (13.05)76.741–3 months, 3 sessions
Control4453.41 (11.94)79.55
Monti 2006 United States [ 74 ]NRParallel groupAnxiety (SCL‐90‐R‐A), depression (SCL‐90‐R‐D), QoL (SF‐36‐mental)AnyNRMindfulness‐based art therapy5653.1 (12.4)1008 weeks, 8 sessions
Control5554.1 (10.7)100
Monti 2012 United States [ 75 ]NRParallel groupAnxiety (SCL‐90‐R‐A)BreastNRMindfulness‐based art therapy855 (5)1008 weeks, 8 sessions
Control1056 (7)100
Monti 2013 United States [ 76 ]NRParallel groupAnxiety (SCL‐90‐R‐A), depression (SCL‐90‐R‐D), QoL (SF‐36‐mental)Breast0‐IVMindfulness‐based art therapy9856.9 (NR)1008 weeks, 8 sessions
Breast cancer support group9356.4 (NR)100
Control4457.4 (NR)100
Mou 2020 China [ 77 ]Cancer centerParallel groupAnxiety (NVAAS)LungNRPre‐recorded music listening15056.99 (9.84)20.671 day, 1 session
Control15057.63 (10.38)18.67
O'steen 2020 China [ 78 ]University radiation therapy centerParallel groupAnxiety (STAI)AnyNRPre‐recorded + live music listening5163 a (NR)1001 day, 1 session
Control5162 a (NR)100
Puig 2006 United States [ 79 ]NRParallel groupAnxiety (POMS‐tension), depression (POMS‐depression)BreastI‐IICreative arts therapy (meditation + poetry)20NR (NR)1004 weeks, 4 sessions
Control19NR (NR)100
Rabinowitch 2023 Israel [ 35 ]OnlineParallel groupAnxiety (STAI‐6)AnyNRMusic therapy14NR (NR)NR1 day, 1 session
Control (meditation)16NR (NR)NR
Raglio 2021 Italy [ 80 ]Cancer centerParallel groupAnxiety (STAI)BreastNRIndividualized pre‐recorded music listening2054.5 a (NR)1002 weeks, 6 sessions
Algorithm‐based pre‐recorded music listening2058 a (NR)100
Control2059 a (NR)100
Romito 2013 Italy [ 81 ]Outpatients in cancer research centerParallel groupAnxiety (emotion thermometer Tool‐A), depression (emotion thermometer Tool‐D)BreastNRMusic therapy and emotional expression3154.14 (NR)1001 day, 1 session
Control3154.21 (NR)100
Rossetti 2017 United States [ 82 ]Cancer centerParallel groupAnxiety (STAI)Breast, head and neckNRMusic therapy3958 a (NR)61.541 day, 1 session
Control3960 a (NR)69.23
Sahan 2024 Turkey [ 83 ]HospitalParallel groupAnxiety (STAI)HematologicNRPre‐recorded music listening3250.7 (13.89)53.131 day, 1 session
Control3252.34 (14.67)59.38
Svensk 2009 Sweden [ 84 ]HospitalParallel groupQoL (WHOQOL‐BREF)BreastNon‐metastaticArt therapy2059.5 a (NR)1005 weeks, 5 sessions
Control2155 a (NR)100
Tang 2021 China [ 85 ]Cancer hospitalParallel groupAnxiety (SAS)Small cell lung carcinomaNRMusic therapy5054.28 (5.59)38.001 day, 1 session
Control5054.28 (5.18)40.00
Tanriverdi 2023 Turkey [ 86 ]HospitalParallel groupAnxiety (STAI), depression (BDI)ColorectalII‐IIIPre‐recorded music listening3251 a (NR)40.632 days, 6 sessions
Control3053 a (NR)40.00
Thyme 2009 Sweden [ 87 ]HospitalParallel groupAnxiety (SCL‐90‐A), depression (SCL‐90‐D)BreastNon‐metastaticArt therapy2059.5 a (NR)1005 weeks, 5 sessions
Control2155 a (NR)100
Tollabzadeh 2023 Iran [ 88 ]HospitalParallel groupAnxiety (Bai)AnyNRPre‐recorded music listening2547.74 (13.96)84.008 weeks, 16 sessions
Control (counseling)2941.14 (9.87)86.21
Tuinmann 2017 Germany [ 89 ]University cancer centerParallel groupAnxiety (HADS‐A), depression (HADS‐D), QoL (EORTC‐QLQ‐C30)Non‐Hodgkin and Hodgkin lymphoma, multiple myeloma, testicular, or leukemiaNRMusic therapy3350.7 (14.6)39.394 weeks, 8 sessions
Control3350.5 (15.4)33.33
UnalToprak 2024 Turkey [ 90 ]HospitalParallel groupAnxiety (HADS‐A), depression (HADS‐D)GynecologicalNRPre‐recorded music listening3059 (12.28)1001 day, 1 session
Control2555.2 (10.54)100
Vachiramon 2013 United States [ 91 ]Dermatologic surgery clinicParallel groupAnxiety (STAI, VAS)SkinNRPre‐recorded music listening5062.6 (14.3)32.001 day, 1 session
Control5066 (13.9)34.00
Yang 2024 Taiwan [ 92 ]HospitalParallel groupAnxiety (Bai‐C)AnyNRPre‐recorded music listening5059.9 (9.6)50.0010 days, 10 sessions
Control5060.3 (11.3)54.00
Yates 2015 United States [ 93 ]Post‐surgical oncology unitParallel groupAnxiety (QMS‐A), depression (QMS‐D)AnyNRLive music listening1357.73 (10.6)84.621 day, 1 session
Control1357.45 (14.24)84.62
Yildirim 2024 Turkey [ 94 ]HospitalParallel groupAnxiety (STAI), depression (BDI)AnyNRMindfulness‐based breathing + music therapy (listening)6057.85 (11.02)36.6710 days, 3 sessions
Control6058.36 (11.09)38.30
Zengin 2013 Turkey [ 95 ]Emergency departmentParallel groupAnxiety (STAI)Any requiring port catheter placementNRPre‐recorded music listening5049 (15.58)44.001 day, 1 session
Control5050.74 (14.01)52.00
Zhou 2011 China [ 96 ]HospitalParallel groupDepression (ZSDS)BreastNRPre‐recorded music listening6044.88 (9.37)10051.4 days, ∼100 sessions
Control6045.13 (9.48)100

Risk of Bias

We determined all studies to be of either moderate or high risk of bias, mainly due to the lack of participant blinding which was not possible given the nature of the intervention. This raised concerns around deviations from intended interventions and measurement of the outcomes, which were largely participant‐reported. We also found many studies to have concerns regarding the randomization process, most commonly due to lack of allocation concealment. A summary of the risk of bias assessments can be found in Figure 2 , and a complete analysis of each individual study's assessments in Supporting Information S2 : Appendix A2.

FIGURE 2 Cochrane risk of bias 2.0 summary plot.
FIGURE 2 Cochrane risk of bias 2.0 summary plot.

Anxiety

For the primary analyses, we found CATs to have a positive effect on anxiety at the immediate (0–6 days) (SMD −0.62 [95% CI −1.01, −0.24]), 4–6 weeks (−1.21 [−2.08, −0.34]), and 2–3 months intervals (−1.19 [−2.14, −0.24]). No significant effect was observed at 1–3 weeks (−0.62 [−1.26, 0.02]) or 4–6 months (−0.85 [−1.92, 0.23]). The results of the meta‐analyses are presented in Table 2 .

TABLE 2
Summary of standardized mean differences (SMD) from meta‐analyses.
Note: For SMD, < 0 indicates improvement (reduction) in Anxiety and Depression and > 0 indicates improvement (increase) in Quality of Life. Abbreviation: k = number of studies.

< 1 week1–3 weeks4–6 weeks2–3 months4–6 months
OutcomekPooled effect (SMD)I 2 (%)kPooled effect (SMD)I 2 (%)kPooled effect (SMD)I 2 (%)kPooled effect (SMD)I 2 (%)kPooled effect (SMD)I 2 (%)
Anxiety22−0.62 [−1.01, −0.24]93.65−0.62 [−1.26, 0.02]92.58−1.21 [−2.08, −0.34]94.87−1.19 [−2.14, −0.24]93.73−0.85 [−1.92, 0.23]89.0
Depression7−0.15 [−0.47, 0.18]64.75−0.44 [−0.87, −0.00]85.05−1.14 [−1.76, −0.52]81.42−0.95 [−3.34, 1.43]93.62−0.18 [−1.19, 0.83]81.1
Quality of life———40.65 [0.05, 1.25]88.741.17 [0.02, 2.32]96.271.42 [0.55, 2.29]94.740.42 [0.04, 0.80]69.0

Subgroup analyses revealed a greater reduction in anxiety at 1–3 weeks for interventions performed in inpatient (−1.11 [−1.62, −0.59]) compared to outpatient settings (0.04 [−0.36, 0.45]) [ 47 ]. Additionally, we found a subgroup effect by region/continent at the 4–6 months interval, with anxiety improving more in West Asian (−1.82 [−2.43, −1.21]) than North American studies (0.04 [−0.56, 0.65]). No subgroup effects were observed for intervention type or session frequency. All forest plots can be found in Supporting Information S3 : Appendix A3.

Depression

In the primary analyses, we found CATs to have a positive effect on depression at the 1–3 weeks (−0.44 [−0.87, −0.00]) and 4–6 weeks intervals (−1.14 [−1.76, −0.05]). The results of the meta‐analyses are presented in Table 2 .

We found evidence of a subgroup effect by intervention type at 4–6 weeks, with music therapy demonstrating a greater effect (−1.60 [−2.02, −1.18]) than art therapy (−0.19 [−0.80, 0.42]). We also observed an effect of intervention setting, with inpatient interventions demonstrating a superior effect to outpatient interventions at the immediate time interval (−0.30 [−0.54, −0.06] vs. 0.43 [0.03, 0.82]) and at 1–3 weeks (−0.77 [−1.12, −0.41] vs. 0.13 [−0.27, 0.54]). Subgroup analyses by region/continent also revealed a subgroup effect at 4–6 weeks with greater improvements observed among East Asian studies (−1.93 [−2.40, −1.47]) compared to those conducted in Europe (−0.19 [−0.80, 0.42]) and North America (−0.82 [−1.47, −0.16]). No subgroup effects were observed for session frequency. Forest plots can be found in Supporting Information S3 : Appendix A3.

Quality of Life

In the primary analyses, we found CATs to have a positive effect on quality of life at all four reported time‐intervals: 1–3 weeks (0.65 [0.05, 1.25]), 4–6 weeks (1.17 [0.02, 2.32]), 2–3 months (1.42 [0.55, 2.29]), and 4–6 months (0.42 [0.04, 0.80]). The results of the meta‐analyses are presented in Table 2 .

We observed a subgroup effect of region/continent at 4–6 weeks and 2–3 months, favoring West Asian studies at both timepoints. At 4–6 weeks, studies conducted in West Asia (4.28 [3.34, 5.22]) produced a greater effect than East Asian (−0.11 [−0.46, 0.23]), European (0.12 [−0.13, 0.38]), and South American studies (0.79 [0.08, 1.50]). At 2–3 months, West Asian studies (1.42 [0.55, 2.29]) produced a greater effect than East Asian (0.74 [0.01, 1.46]), European (0.61 [−0.01, 1.24]), and North American studies (0.38 [−0.87, 1.64]). No subgroup effects were observed for intervention type or setting. We were unable to perform subgroup analyses by session frequency because there were insufficient studies within each subgroup that reported quality of life at comparable time points. Forest plots can be found in Appendix A3.

Publication Bias

The only meta‐analysis with more than 10 studies was anxiety at the immediate time interval, in which we found no evidence of publication bias upon visual inspection of the funnel plot. Funnel plot can be found in Appendix A3.

Qualitative Results

Twenty‐two studies were not included in the meta‐analyses due to lack of reporting of the necessary statistics (i.e., sample sizes, central tendencies, and/or measure of dispersion). Of these, 21 reported on anxiety, 11 on depression, and 5 on quality of life. CATs were associated with a significant reduction in anxiety in 66.7% of studies ( n = 14); for depression, CATs were associated with a significant reduction in 45.5% of studies ( n = 5); for quality of life, CATs were associated with a significant improvement in quality of life in 40% of studies ( n = 2). A table summarizing the results of the qualitative analysis can be found in Table 3 .

TABLE 3
Summary of qualitative results.
Abbreviations: = significant improvement ( p < 0.05) with CAT, = no change ( p > 0.05) with CAT, = significant negative effect ( p < 0.05) with CAT.

StudyAnxietyDepressionQuality of life
Alam 2016——
Alcântara‐silva 2018—
Bradt 2024——
Bro 2019——
Bulfone 2009——
Cassileth 2003—
Chen 2013——
Chen 2018—
Clark 2006—
Du 2024——
Firmeza 2017——
Giordano 2023——
Lazaro‐Garcia 2024
McCabe 2013—
Mondanaro 2021—
Monti 2006
Monti 2013
O'steen 2020——
Raglio 2021——
Romito 2013—
Rossetti 2017——
Tuinmann 2017

GRADE Assessment

The GRADE assessment of the certainty of the evidence revealed low‐to‐very low certainty evidence for all of the outcomes, mostly due to the substantial risk of bias among included studies and unexplained heterogeneity. The GRADE assessments are summarized in Table 4 .

TABLE 4
GRADE evidence profile.
Note: For SMD, < 0 indicates improvement (reduction) in Anxiety and Depression and > 0 indicates improvement (increase) in Quality of Life. Abbreviation: SMD = standardized mean difference.

OutcomeTimeframeStudies ( n )Certainty assessmentCertainty of evidence rating & relative effect size
Risk of biasInconsistencyIndirectnessImprecisionPublication bias
AnxietyImmediate22 (1967)Some limitationsSome limitationsNo limitationsNo limitationsNo limitationsLow
SMD −0.62 [−1.01, −0.24]
1–3 weeks5 (549)Some limitationsSome limitationsNo limitationsSome limitationsNo limitationsVery low
SMD −0.62 [−1.26, 0.02]
4–6 weeks8 (526)Some limitationsSome limitationsNo limitationsNo limitationsNo limitationsLow
SMD −1.21 [−2.08, −0.34]
2–3 months7 (386)Some limitationsSome limitationsNo limitationsNo limitationsNo limitationsLow
SMD −1.19 [−2.14, −0.24]
4–6 months3 (143)Some limitationsSome limitationsNo limitationsSome limitationsNo limitationsVery low
SMD −0.85 [−1.92, 0.23]
DepressionImmediate7 (465)Some limitationsSome limitationsNo limitationsSome limitationsNo limitationsVery low
SMD −0.15 [−0.47, 0.18]
1–3 weeks5 (569)Some limitationsSome limitationsNo limitationsNo limitationsNo limitationsLow
SMD −0.44 [−0.87, 0.00]
4–6 weeks5 (278)Some limitationsSome limitationsNo limitationsNo limitationsNo limitationsLow
SMD −1.14 [−1.76, −0.52]
2–3 months2 (66)Some limitationsSome limitationsNo limitationsSome limitationsNo limitationsVery low
SMD −0.95 [−3.34, 1.43]
4–6 months2 (83)Some limitationsSome limitationsNo limitationsSome limitationsNo limitationsVery low
SMD −0.18 [−1.19, 0.83]
Quality of life1–3 weeks4 (430)Some limitationsSome limitationsNo limitationsNo limitationsNo limitationsLow
SMD 0.65 [0.05, 1.25]
4–6 weeks4 (460)Some limitationsSome limitationsNo limitationsNo limitationsNo limitationsLow
SMD 1.17 [0.02, 2.32]
2–3 months7 (540)Some limitationsSome limitationsNo limitationsNo limitationsNo limitationsLow
SMD 1.42 [0.55, 2.29]
4–6 months4 (440)Some limitationsSome limitationsNo limitationsNo limitationsNo limitationsLow
SMD 0.42 [0.04, 0.80]

Discussion

The results of this systematic review and meta‐analyses of 67 randomized controlled trials suggest that creative arts therapies may be effective in improving psychological outcomes in cancer patients. In particular, our meta‐analyses found that creative arts therapies may reduce depression and anxiety for up to 6 weeks and 3 months post‐treatment, respectively, and improve quality of life up to 6 months post‐treatment. The qualitative analyses support these findings, particularly in the outcome of anxiety.

Our results, which found CATs to reduce anxiety and depression among cancer patients, are in alignment with previous evidence syntheses on the topic [ 17 , 18 , 20 , 21 , 97 ]. This effect is likely driven by the ability of CATs to induce relaxation and regulate the cognitive and emotional systems [ 98 ]. While the exact mechanism behind this remains unclear, preliminary evidence suggests that creative arts consistently activate neural circuits involved in emotional regulation, including the medial prefrontal cortex and amygdala; this may indicate a shared cognitive pathway between creative expression and emotional processing [ 99 ]. We also found that CATs were most effective in treating anxiety and depression when applied in an inpatient setting compared to an outpatient setting. Given that hospitalized cancer patients are likely to have a higher baseline level of anxiety and depression [ 100 ], it may be that psychological relief is simply most needed in the hospital.

Interestingly, we found that music therapy had the largest effect on depression, although it is important to note that this was observed only at the 4–6 weeks timepoint. There is substantial evidence supporting the ability of music to regulate mood [ 101 , 102 ]. These benefits are likely due to music's ability to engage interconnected brain regions involved in emotion and reward processing, including the amygdala, hippocampus, nucleus accumbens, and prefrontal cortex; ultimately, this activation is thought to improve emotional regulation, reduce stress, and enhance feelings of pleasure [ 103 ]. Moreover, music is intrinsically enjoyable and facilitates verbal and non‐verbal expression of emotion [ 104 ], which likely further contributes to its benefits. While CATs broadly appear to reduce depression, music may be the most effective way of providing system regulation in cancer patients.

We found CATs to improve quality of life up to 6 months post‐treatment. Previous reviews report mixed results: while most report an improvement in overall quality of life [ 17 , 19 , 20 , 21 , 97 ], some report no benefit at all or only in specific sub‐dimensions like social or physical quality of life [ 18 , 19 , 22 ]. In addition to the psychophysiological benefits described previously, CATs have been said to promote a sense of personal agency, hope, personal connection, emotional awareness, and flow state [ 104 ] that may not only induce improvements in clinical outcomes, but also provide existential relief and a sense of meaning for cancer patients.

The only subgroup effect consistently observed across all three outcomes was the effect of region. We found that studies conducted in Asian countries, and thus Asian populations, were associated with a higher effect size. It is first important to acknowledge the risk of bias and large effect sizes observed in some of the included studies; effect estimates should be interpreted cautiously. That being said, these geographic differences may be a result of cultural differences between Western and Asian societies: Asian cultures tend to be more collectively oriented, have traditional roots in mindfulness and acceptance‐based philosophies, and place less emphasis on emotional expression [ 105 ]. CATs typically encourage creative expression and self‐engagement, both of which also contribute to their therapeutic effect [ 104 ]. CATs may therefore be particularly effective in populations where emotional expression is not the norm and there is an established amenability to artistic or mindfulness interventions.

Clinical and Research Implications

Both our meta‐analyses and qualitative findings support the use of creative arts therapies as a potentially effective psychosocial intervention for improving anxiety, depression, and quality of life in cancer patients.

There may be greater clinical benefits of implementing CATs in the hospital compared to outpatient settings, particularly for anxiety and depression. However, this may owe to the higher baseline levels of anxiety and depression observed in hospitalized cancer patients [ 100 ], such that they are more likely to reap greater benefits from CATs. To explore this further, studies comparing the effect of CATs in hospitalized versus non‐hospitalized patients and controlling for baseline psychological symptom levels are of interest.

Compared to other intervention types, music‐based internventions may be the most effective in improving depression for cancer patients. These include music therapy sessions led by a registered music therapist (e.g., active “music‐making” interventions), but can also encompass lower‐cost alternatives such as listening to pre‐recorded music. For patients facing complex socioeconomic challenges, the latter may offer an affordable and accessible way to support mood regulation.

Across anxiety, depression, and quality of life, CATs appear to offer the greatest benefit in Asian countries. Clinicians working in Asian settings, or with Asian populations in other regions, may consider prioritizing CATs as a culturally responsive intervention. Additionally, this highlights the importance of tailoring psychosocial interventions to specific cultural contexts rather than adopting a one‐size‐fits‐all approach.

Strengths and Limitations

This study has many strengths. We conducted a quantitative and qualitative synthesis of 67 randomized trials on three clinically important psychological outcomes for cancer patients, utilizing the best practices in evidence synthesis (i.e., independent and in duplicate screening and extraction; risk of bias assessment; certainty of the evidence assessment). Our analyses were stratified by time‐point to reduce heterogeneity and provide important context on the longevity of effects from CATs in cancer patients. We also conducted several subgroup analyses of important factors that influence treatment effect, such as intervention type, session frequency, intervention setting, and region. These subgroup analyses help to identify optimal protocols.

This study was limited by our inclusion of English studies only; however, we identified 67 randomized trials and only excluded four studies due to non‐English language, which gives us confidence in the representativeness of our sample. Additionally, despite multiple subgroup analyses, we were unable to explain much of the heterogeneity observed in the primary analyses. Heterogeneity may also have been introduced by differences in measurement tools across studies. Although all tools used have established validity in oncology or psychosocial research, differences in sensitivity, specificity, scaling, and psychometric properties may have influenced the comparability of observed effects. Lastly, many studies were rated as having high risk of bias, which may have contributed to inflated effect estimates. Nevertheless, the observed effects of CATs were generally consistent in direction across studies and outcomes, suggesting an overall benefit despite limitations in study quality.In conjunction with the certainty of evidence ratings, the results of these meta‐analyses should be interpreted judiciously.

Conclusion

Creative arts therapies may reduce anxiety and depression and improve quality of life among cancer patients. Meta‐analyses suggest that reductions in depression may persist for up to 6 weeks post‐intervention, anxiety up to 3 months, and quality‐of‐life improvements up to 6 months. Music‐based interventions, including both therapist‐led sessions and lower‐cost listening interventions, may be particularly effective for improving depressive symptoms. Greater effects were observed in inpatient settings and in Asian countries, highlighting the importance of contextual and cultural considerations. Collectively, these findings support the integration of creative arts therapies into comprehensive cancer care to address anxiety, depression, and quality of life.

This review advances prior evidence syntheses by providing methodological elements that have been largely absent from earlier reviews, include a focused meta‐analysis of randomized controlled trials with stratification by follow‐up time points, subgroup analyses of potential sources of heterogeneity, and a certainty of evidence assessment using GRADE. At the same time, the findings highlight important limitations in the existing literature and underscore the need for high‐quality randomized controlled trials to strengthen the evidence base and inform clinical practice.

Author Contributions

Ashlyn S. L. Chou: conceptualization, formal analysis, methodology, project administration, software, validation, visualization, writing – original draft, writing – review and editing. Tyler McKechnie: conceptualization, formal analysis, methodology, validation, visualization. Vikram Arora: formal analysis, software, validation, visualization. Brianna DePestel: conceptualization, methodology, software, validation. Austine Wang: conceptualization, methodology, software, validation. Sameer Parpia: methodology, supervision, validation, writing – review and editing. Goran Calic: supervision, validation, writing – review and editing. Phillip Staibano: supervision, validation, writing – review and editing. Alexandra Derus: writing – review and editing. Akanksha Guleria: writing – review and editing. Mohit Bhandari: conceptualization, formal analysis, methodology, project administration, supervision, validation, writing – review and editing. Alex Thabane: conceptualization, formal analysis, methodology, project administration, software, supervision, validation, visualization, writing – original draft, writing – review and editing.

Ethics Statement

This review was exempt from ethical approval as it involved the analysis of published literature.

Consent

This review has been registered under PROSPERO as “Effectiveness of creative arts therapies in improving anxiety, depression and quality of life in adult cancer patients: A systematic review and meta‐analysis” and registration number CRD420251087592. A protocol was not prepared.

Conflicts of Interest

The authors declare no conflicts of interest.

Supporting information

Supporting Information S1

Supporting Information S2

Supporting Information S3

Acknowledgements

The authors have nothing to report.

Funding

The authors have nothing to report.

Data Availability Statement

The data that support the findings of this study are available from the corresponding author upon reasonable request.

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Associated Data

Supplementary Materials

Supporting Information S1

Supporting Information S2

Supporting Information S3

Data Availability Statement

The data that support the findings of this study are available from the corresponding author upon reasonable request.

ИП Урсолов Владлен Сергеевич

ИНН 500118482352 · ОГРНИП 314500117700049

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