Integrated Psychological Program for Management of Postnatal Depression and Persistent Postpartum Pain After Childbirth (CODEPAD-II)
Depression, Postpartum
About this trial
This is an interventional prevention trial for Depression, Postpartum
Eligibility 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.
Sites / Locations
- KK Women's and Children's HospitalRecruiting
Arms of the Study
Arm 1
Arm 2
Experimental
No Intervention
Integrated psychological program (IPP) group
Non- 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.
Questionnaires on psychological and pain assessments will be administered before and after delivery, with the final time point being 2 months after delivery.