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NCT06597448
Public Health Nurse-Peer Co-Led Group Cognitive Behavioral Therapy for Postpartum Depression
NA trial testing Cognitive Behavioral Therapy for Postpartum Depression (PPD) in Postpartum Depression in 170 participants. Participants enrolled and being followed up; not accepting new ones.
1 June 2027
Quick facts
| Lead sponsor | McMaster University |
|---|---|
| Phase | NA |
| Status | Active, enrolled |
| Study type | INTERVENTIONAL |
| Allocation | randomized |
| Design | parallel |
| Masking | double |
| Primary purpose | treatment |
| Enrollment | 170 |
| Start date | 16 September 2024 |
| Primary completion | 1 June 2027 |
| Estimated completion | 1 January 2028 |
| Sites | 1 location across Canada |
Drugs / interventions tested
- Cognitive Behavioral Therapy for Postpartum Depression (PPD)
Conditions studied
- Postpartum Depression — all drugs for Postpartum Depression →
Sponsor
McMaster University
Who can join
18 and older, female only, with Postpartum Depression. Patients with the condition only — healthy volunteers not accepted.
Sponsor's own description
The purpose of this study is to determine the effectiveness of an online 9-week group Cognitive Behavioural Therapy (CBT; a type of talking therapy) intervention that is co-led by public health nurses (PHNs) and individuals who have previously recovered (i.e., lay peers) from postpartum depression (PPD) for treating PPD when delivered in addition to treatment as usual (TAU) compared to TAU alone. The study will also assess the impact of the intervention on common comorbidities (anxiety) and complications (parenting stress, mother-infant relationship, social support, and infant temperament) of PPD and whether it is cost-effective.
Publications & conference data
No peer-reviewed publications indexed yet for this trial.
Verify or expand the search:
- PubMed search for NCT06597448
- Europe PMC full search
- ASCO Meeting Library
- ESMO Meeting Library
- bioRxiv preprints
- medRxiv preprints
- Google Scholar
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Verify against primary sources
- ClinicalTrials.gov — authoritative US registry record
- WHO ICTRP — international registry index
- EU Clinical Trials Register
- Sponsor press releases (Google)
- Trial protocol + status: ClinicalTrials.gov NCT06597448 (US National Library of Medicine, public domain)
- Drug + disease cross-links: matched in real time against Drug Landscape's normalised drug + company + condition tables
- Sponsor: as reported to ClinicalTrials.gov by McMaster University
- Last refreshed: 9 December 2025
Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT06597448.
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