Online workshops to prevent postpartum depression
Online 1-Day CBT-Based Workshops for Preventing Postpartum Depression: A Randomized Controlled Trial
NA · McMaster University · NCT05753176
This study tests if an online workshop can help pregnant women in their third trimester lower their chances of developing postpartum depression after giving birth.
Quick facts
| Phase | NA |
|---|---|
| Study type | Interventional |
| Enrollment | 408 (estimated) |
| Ages | 18 Years and up |
| Sex | Female |
| Sponsor | McMaster University (other) |
| Locations | 1 site (Hamilton, Ontario) |
| Trial ID | NCT05753176 on ClinicalTrials.gov |
What this trial studies
This clinical trial examines the effectiveness of an online cognitive behavioral therapy (CBT)-based workshop designed to prevent postpartum depression (PPD) in pregnant women during their third trimester. The study will involve 408 participants who will be randomly assigned to either the workshop plus usual treatment or usual treatment alone. The primary outcome will be measured using the Edinburgh Postnatal Depression Scale (EPDS) two months postpartum. The goal is to provide an accessible and efficient intervention to reduce the incidence of PPD, which affects many new mothers.
Who should consider this trial
Good fit: Ideal candidates for this study are pregnant women aged 18 and older, currently in their third trimester, residing in Ontario, Canada, and at risk for postpartum depression.
Not a fit: Patients currently experiencing a major depressive episode or those with certain psychiatric disorders may not benefit from this study.
Why it matters
Potential benefit: If successful, this intervention could significantly reduce the rates of postpartum depression among new mothers.
How similar studies have performed: Other studies have shown success with similar CBT-based interventions for mental health, indicating potential for this approach in preventing postpartum depression.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: * 18 years of age or older * Currently residing in Ontario, Canada * Currently in 3rd trimester of pregnancy (28-36 weeks gestation) * EPDS score \>6 * Past history of major depressive disorder (determined using the Mini International Neuropsychiatric Interview (MINI) Exclusion Criteria: * positive score on the MINI for a current major depressive episode * positive score on the MINI subsections of bipolar, psychotic, or borderline personality disorder
Where this trial is running
Hamilton, Ontario
- McMaster University — Hamilton, Ontario, Canada (RECRUITING)
Study contacts
- Principal investigator: Ryan J Van Lieshout, MD, PhD — McMaster University
- Study coordinator: Ryan J Van Lieshout, MD, PhD
- Email: vanlierj@mcmaster.ca
- Phone: 905-522-1155
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.
Conditions: Postpartum Depression, Postpartum Anxiety, cognitive behavioral therapy, CBT, postpartum depression, PPD, randomized controlled trial, RCT