Effect of Moxibustion Intervention on Insomnia Patients

Status Recruiting

Clinical Trial Summary

Clinical Trial Description

Type of study:clinical trial Purpose of research:To explore the efficacy and safety of moxibustion combined with Traditional Chinese and Western medicine in treating insomnia. Describe participant population/health conditions:120 insomnia patients The participants were enrolled according to the principle of randomization and single blindness, and the analysis was adjusted every quarter according to the research schedule. The study group was treated with traditional Chinese moxibustion and western medicine. The control group was treated with only western medicine. Clinical evaluation of the main efficacy indicators: The score of PSQI scale was assessed. The reduction rate of PSQI scale was ≥ 25% as effective, and the difference between the two groups was compared as the basis for evaluating the main efficacy indicators. The efficacy of insomnia symptoms was evaluated by the difference of PSQI score reduction rate between groups before and after intervention. Secondary clinical outcome measures: Quality of Life Scale (SQLS), SF-36 scale, Clinical Gross Impression Scale (CGI), adverse reaction（TESS） . ;

Study Design

Related Conditions & MeSH terms

Insomnia
Moxibustion
Sleep Initiation and Maintenance Disorders

Clinical Trial Details

NCT number	NCT06171308
Study type	Interventional
Source	Shanghai Mental Health Center
Contact	JING Cai, Undergraduate
Phone	13524000307
Email	1994510cj@163.com
Status	Recruiting
Phase	N/A
Start date	January 1, 2023
Completion date	December 31, 2025

View Details

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