Program to manage postnatal depression and pain after childbirth
Integrated Psychological Program for Management of Postnatal Depression and Persistent Postpartum Pain After Childbirth: CODEPAD - II (Collaborative Outcomes of DEpression and Pain Associated With Delivery- II)
This study is testing a new program that combines mindfulness, music, and online counseling to help new mothers with postnatal depression and pain after childbirth.
Quick facts
| Phase | Not applicable |
|---|---|
| Study type | Interventional |
| Enrollment | 1480 (estimated) |
| Ages | 21 Years to 50 Years |
| Sex | Female |
| Sponsor | KK Women's and Children's Hospital Government |
| Locations | 1 site (Singapore) |
| Trial ID | NCT05285215 on ClinicalTrials.gov |
What this trial studies
This integrated psychological program (IPP) aims to address postnatal depression (PND) and persistent postpartum pain (PPP) through a combination of mindfulness training, music listening, and digital health video counseling. The program leverages technology to provide outpatient care, making it accessible for new mothers. By monitoring and treating PND and PPP, the study seeks to improve maternal health outcomes and enhance mother-child bonding. A total of 1480 women will participate in this randomized controlled trial to evaluate the effectiveness of the IPP.
Who should consider this trial
Good fit: Ideal candidates are healthy women at term with a singleton fetus who are delivering at the participating institution.
Not a fit: Patients currently receiving active psychiatric care or with a history of chronic pain syndrome may not benefit from this program.
Why it matters
Potential benefit: If successful, this program could significantly reduce the incidence of postnatal depression and improve overall maternal well-being.
How similar studies have performed: Other studies have shown promise in using integrated psychological approaches for managing postpartum conditions, suggesting potential for success in this novel application.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: * healthy (American Society of Anesthesiologists physical status 2) * parturient women at term (36 weeks' gestation or more, nulliparous and multiparous); * with a singleton fetus; * to have delivery in this institution. Exclusion Criteria: * current active psychiatric care; * history of intravenous drug or opioid abuse; * previous history of chronic pain syndrome.
Where this trial is running
Singapore
- KK Women's and Children's Hospital — Singapore, Singapore (Recruiting)
Study contacts
- Principal investigator: Ban Leong Sng — KK Women's and Children's Hospital
- Study coordinator: Ban Leong Sng
- Email: sng.ban.leong@singhealth.com.sg
- Phone: +65 6394 1077
How to participate
- Review the eligibility criteria above with your treating physician.
- Visit the official trial page on ClinicalTrials.gov for the most current contact information and recruitment status.
- Contact the listed study coordinator or principal investigator to request pre-screening. Pre-screening is free and never obligates you to enroll.