← Back to Clinical Trials
Recruiting NCT06275217

NCT06275217 Mindful Yoga for Postpartum Depression

◆ AI Clinical Summary
Plain-language summary for patients
Clinical Trial Summary
NCT ID NCT06275217
Status Recruiting
Phase
Sponsor The Hong Kong Polytechnic University
Condition Mood Disorders
Study Type INTERVENTIONAL
Enrollment 198 participants
Start Date 2021-01-08
Primary Completion 2025-07-15

Trial Parameters

Condition Mood Disorders
Sponsor The Hong Kong Polytechnic University
Study Type INTERVENTIONAL
Phase N/A
Enrollment 198
Sex FEMALE
Min Age 18 Years
Max Age 60 Years
Start Date 2021-01-08
Completion 2025-07-15
Interventions
Mindfulness-based yoga programPsychoeducation

Eligibility Fast-Check

Enter your details for a quick preliminary check. This does not replace medical advice.

Brief Summary

This is a parallel-group randomized controlled trial. A total of 198 postpartum women with depressive symptoms (EPDS scores≥8 at baseline) will be recruited and randomized into two groups: 10-week mindful yoga intervention and 10-week psychoeducation program. Clinical assessment of depression, self-report questionnaires and salivary cortisol tests will be performed at baseline, after 10-week intervention, and at 6-month and 12-month follow-ups. The investigators expected that the mindful yoga intervention will reduce depression after 10 weeks compared to psychoeducation. The mindful yoga intervention will further reduce anxiety, stress, improve quality of life and sleep, and steepen diurnal cortisol slopes. These effects will be maintained for at least six months.

Eligibility Criteria

Inclusion Criteria: * Postpartum women aged 18-60 years old. * The scores of EPDS ≥ 10. * At least 6 week and up to 1 year after childbirth. * Giving birth to a single full-term healthy baby (gestation between 37-41 weeks, body weight \> 2.5kg, APGAR score at 5 minutes \> 7). * Fewer than 10 hours of yoga/Qi gong/Tai Chi or mindfulness/meditation practice in the previous 3 months. Exclusion Criteria: * Severe complications after delivery, or their infants are admitted to NICU. * Regular psychiatric follow-up. * Currently taking antipsychotic drugs. * Known pragnancy, or other contraindications to physical exercise (e.g., wound healing situation) according to the body examination by O\&G clinicians at 6 weeks after delivery.

Related Trials

ClinicalMetric — Independent clinical trial intelligence platform. Not affiliated with NIH, ClinicalTrials.gov, the U.S. FDA, or any pharmaceutical company, hospital, or clinical research organization. Trial data is sourced from ClinicalTrials.gov for informational purposes only and does not constitute medical advice. Do not make any treatment, enrollment, or health decisions based solely on information found here — always consult a qualified healthcare professional. Full Disclaimer  ·  Last Reviewed: April 2026  ·  Data Methodology