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Life sciences · Interventional Study
ClinicalTrials.gov · November 9, 2026
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Interventional Study.
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Registry record from ClinicalTrials.gov (NCT07376395). This is a study registration, not published results. Lead sponsor: Istanbul University - Cerrahpasa. Recruitment status: RECRUITING. Phase: NA. Study type: INTERVENTIONAL. Enrollment: 60 participants (ESTIMATED). Conditions: Quality of Life, Depression, Anxiety, Stress. Interventions: BEHAVIORAL: General Health Education; BEHAVIORAL: Jin Shin Jyutsu®-Based Hand Application. Primary outcome measures: Descriptive Information Form , Day 1 (Baseline, Pre-Intervention); Coping Strategies , Day 1 (Baseline, before the Jin Shin Jyutsu intervention or standardized health education) and Day 14 (Post-intervention/follow-up assessment).; Menopause-Specific Quality of Life , Day 1 (Baseline, before the Jin Shin Jyutsu intervention or standardized health education) and Day 14 (Post-intervention/follow-up assessment).; Distress Thermometer , Day 1 (Baseline, before the Jin Shin Jyutsu intervention or standardized health education) and Day 14 (Post-intervention/follow-up assessment).; Depression, Anxiety, and Stress , Day 1 (Baseline, before the Jin Shin Jyutsu intervention or standardized health education) and Day 14 (Post-intervention/follow-up assessment).; Daily Practice Schedule for JSJ®-Based Hand Application , The intervention group will complete this chart for 14 days.. Brief summary: This randomized controlled study aims to evaluate the effect of a Jin Shin Jyutsu®-based hand application guided by the Transactional Model of Stress and Coping on quality of life and psychosocial status in perimenopausal women. Participants in both groups will receive standardized verbal health education related to perimenopause and menopause. In addition, participants in the experimental group will perform a standardized Jin Shin Jyutsu®-based hand application for 5 minutes daily for 14 consecutive days. Outcomes related to quality of life, coping, psychological distress, depression, anxiety, and stress will be assessed at baseline and after the 14-day study period.