Online PHN CBT for PPD
Postpartum Depression
About this trial
This is an interventional treatment trial for Postpartum Depression
Eligibility Criteria
Inclusion Criteria:
- Eligible women will be >18 years of age, understand and speak English (so that they can participate in the CBT group and complete study measures), have an EPDS score between of 10 or more and meet diagnostic criteria for current major depressive disorder on the Mini International Neuropsychiatric Interview-Plus (MINI-Plus). They will also all be within 12 months of delivering an infant.
Exclusion Criteria:
- In order to increase the relevance and generalizability of our findings, women can have psychiatric comorbidities with the exception of bipolar disorder, a current psychotic, substance or alcohol use disorder, or antisocial or borderline personality disorder. These are predictors of significant difficulty participating in therapy groups and/or non-response to CBT.
Sites / Locations
- McMaster University
Arms of the Study
Arm 1
Arm 2
Experimental
No Intervention
Treatment (9-week online CBT group)
Control (treatment as usual)
Participants assigned to the treatment group will participate in a 9-week group CBT intervention for PPD delivered via Zoom by two public health nurses. This intervention was developed by Dr. Van Lieshout (PI) at the Women's Health Concerns Clinic (WHCC) at St. Joseph's Healthcare Hamilton. It was designed to be brief, simple, and applicable to women in community settings. It consists of 9 weekly 2-hour sessions where core CBT skills are learned and practiced, and a new psychoeducational topic is introduced and discussed by women each week. All participants in the treatment group will be mailed a hardcopy of the program manual.
The control group will receive standard postnatal care from Niagara Region Public Health, their obstetrician, midwife, and/or family physician.