Effectiveness of Mindfulness-Based Resilience Promotion Programs
Not Applicable
- Conditions
- Healthy adults
- Registration Number
- JPRN-UMIN000051536
- Lead Sponsor
- Kawasaki University of Medical Welfare
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Pending
- Sex
- All
- Target Recruitment
- 50
Inclusion Criteria
Not provided
Exclusion Criteria
Those who practice mindfulness or mindfulness-like yoga, meditation or breathing exercises on a daily basis. Those who are currently undergoing cognitive behavioural therapy. Those at significant risk of postpartum depression, dementia, intellectual disability, self-harm or other harm. Those taking multiple antipsychotic medications (chlorpromazine equivalent 600 mg/day or more).
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method The primary outcome measures are skin potential and heart rate, and fluctuations in skin potential and heart rate due to stress loading are assessed. Skin potential is measured using Thought Technology's "ProComp Vital Monitor FlexComp". Heart rate is measured using "myBeat" by UNION TOOL. Three evaluation periods were used. Specifically, immediately before the intervention (T0), immediately after the 4-week intervention (T1) and 4 weeks after the intervention (T2).
- Secondary Outcome Measures
Name Time Method