Medicine · 2022
Efficacy and safety evaluation of adjuvant auricular acupuncture for smoking cessation: A study protocol of randomized, assessor-blinded, pragmatic pilot trial.
Протокол клинического исследованияСтатьяНазвание и аннотация: Перевод в очереди
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Sung Won-Suk, Choi In Suh, Moon Jeong-Hyun, Chae Soo-Yeon, Jo Min-Gi, Kim Jung-Hyun, Park Yeon-Cheol, Kim Eun-Jung, Baek Yong-Hyeon, Kim Geun-Woo, Seo Byung-Kwan
Аннотация
BACKGROUND: Smoking negatively impacts public health. There are several treatments to quit smoking, and nicotine replacement treatment (NRT) reportedly doubles the smoking cessation rate, with some limitations. Acupuncture is an alternative option with proven effects on smoking cessation. However, there has been no definite report that indicates the efficacy and safety of auricular acupuncture (AA) combined with NRT on smoking cessation.
METHODS: This is a randomized, assessor-blind, and pragmatic pilot study. We will recruit 40 participants who want to stop smoking and randomly allocate them into an NRT group and an NRT + AA group with a 1:1 ratio. Participants will receive NRT for 4 weeks and the NRT + AA group will receive additional AA treatment with 5 AA points (Shenmen (TF4), lung (CO14), throat (TF3), inner nose (TG4), and endocrine (CO18)) twice a week for 4 weeks. Follow-up will be conducted 1 and 3 months after intervention completion. The primary outcome will be tobacco consumption and abstinence rate determined by calculating the rate of change in cigarette use and a urine test. Secondary outcomes will be the quality of life (EuroQol-5D and visual analogue scale), nicotine dependence (Fagerstrom test for nicotine dependence), nicotine withdrawal (Minnesota nicotine withdrawal scale), physical effects, satisfaction, and safety measurement (adverse events).
RESULTS: We will investigate the efficacy and safety of AA combined with NRT treatment for smoking cessation.
CONCLUSION: Our study will provide additional clinical evidence for AA as an adjuvant treatment for smoking cessation.
TRIAL REGISTRATION NUMBER: Clinical Research Information Service (registration number: KCT0007212).
METHODS: This is a randomized, assessor-blind, and pragmatic pilot study. We will recruit 40 participants who want to stop smoking and randomly allocate them into an NRT group and an NRT + AA group with a 1:1 ratio. Participants will receive NRT for 4 weeks and the NRT + AA group will receive additional AA treatment with 5 AA points (Shenmen (TF4), lung (CO14), throat (TF3), inner nose (TG4), and endocrine (CO18)) twice a week for 4 weeks. Follow-up will be conducted 1 and 3 months after intervention completion. The primary outcome will be tobacco consumption and abstinence rate determined by calculating the rate of change in cigarette use and a urine test. Secondary outcomes will be the quality of life (EuroQol-5D and visual analogue scale), nicotine dependence (Fagerstrom test for nicotine dependence), nicotine withdrawal (Minnesota nicotine withdrawal scale), physical effects, satisfaction, and safety measurement (adverse events).
RESULTS: We will investigate the efficacy and safety of AA combined with NRT treatment for smoking cessation.
CONCLUSION: Our study will provide additional clinical evidence for AA as an adjuvant treatment for smoking cessation.
TRIAL REGISTRATION NUMBER: Clinical Research Information Service (registration number: KCT0007212).