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Life sciences · Interventional Study
ClinicalTrials.gov · October 2, 2026
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Interventional Study.
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Registry record from ClinicalTrials.gov (NCT07669805). This is a study registration, not published results. Lead sponsor: Buddhist Tzu Chi General Hospital. Recruitment status: RECRUITING. Phase: NA. Study type: INTERVENTIONAL. Enrollment: 50 participants (ESTIMATED). Conditions: Depression and/or Anxiety in the Mild-to-moderate Range, Loneliness, Social Isolation. Interventions: BEHAVIORAL: Mindfulness Lifestyle Social Prescribing Program. Primary outcome measures: Changes in Geriatric Depression Scale (GDS-15) score , Baseline and Week 8; Changes in UCLA Loneliness Scale score , Baseline and Week 8; Changes in WHOQOL-BREF questionnaire score , Baseline and Week 8. Brief summary: The goal of this clinical trial is to evaluate the effectiveness of an 8-week mindfulness lifestyle social prescribing program in community-dwelling older adults aged 55 and older. The main questions it aims to answer are: To establish a mindfulness lifestyle social prescribing model applied to the psychological and social health promotion of middle-aged and older populations. To evaluate the effectiveness of the intervention on improving depressive symptoms, loneliness, and quality of life in this population. Participants will receive an 8-week group intervention program, with each weekly session lasting approximately 3 hours. The structured curriculum integrates mindfulness awareness, body scanning, mindfulness stretching, breathing training, healthy dietary education, and art practices (such as herbal therapy and leaf printing). Researchers will collect and evaluate data from pre- and post-intervention assessments to measure changes in depressive symptoms, loneliness risk, and overall quality of life.