Postpartum Depression Clinical Trials

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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)

Status: Completed
Location: See location...
Intervention Type: Procedure
Study Type: Interventional
Study Phase: Not Applicable
SUMMARY

The integrated psychological program (IPP) is based on evidence from the local population showing that the interventional components (mindfulness training, music listening, video counselling) are amenable to implementation in the outpatient care setting. Incorporating innovative digital mobile and electronic applications in the care of an increasingly technology-savvy population will be strategic. The proposal will transform the healthcare model for treating postnatal depression (PND) and persistent postpartum pain (PPP).

Eligibility
Participation Requirements
Sex: Female
Minimum Age: 21
Maximum Age: 50
Healthy Volunteers: f
View:

• 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.

Locations
Other Locations
Singapore
KK Women's and Children's Hospital
Singapore
Time Frame
Start Date: 2022-04-18
Completion Date: 2025-12-05
Participants
Target number of participants: 1720
Treatments
Experimental: Integrated psychological program (IPP) group
Patients are assigned to have mindfulness training and music listening before and after delivery. Video counselling will be offered if patient is found to have Edinburgh Postnatal Depression Scale (EPDS) equal to or more than 10. Questionnaires on psychological and pain assessments will be administered before and after delivery, with the final time point being 2 months after delivery.
No_intervention: Non- Integrated psychological program (IPP) group
Questionnaires on psychological and pain assessments will be administered before and after delivery, with the final time point being 2 months after delivery.
Related Therapeutic Areas
Sponsors
Leads: KK Women's and Children's Hospital

This content was sourced from clinicaltrials.gov