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NCT03793569

Does Enhancing Maternal Peer Interactions Decrease Rates of Postpartum Depression?

Completed NA Last updated 22 August 2019
What this trial tests

NA trial testing Peer discussion group in Postpartum Depression in 33 participants. Completed in 30 July 2019.

Timeline
27 August 2018
Primary endpoint
30 July 2019
30 July 2019

Quick facts

Lead sponsorMilton S. Hershey Medical Center
PhaseNA
StatusCompleted
Study typeINTERVENTIONAL
Allocationrandomized
Designparallel
Maskingnone
Primary purposeprevention
Enrollment33
Start date27 August 2018
Primary completion30 July 2019
Estimated completion30 July 2019
Sites1 location across United States

Drugs / interventions tested

Conditions studied

Sponsor

Milton S. Hershey Medical Center

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 long-term goal of this study is to validate a simple and inexpensive intervention to reduce the incidence and impact of Postpartum Depression (PPD). The central hypothesis is that enhancing social support of new mothers specifically via an organized peer get-together will decrease rates of postpartum depression. The rationale for the proposed research is that even though PPD is common and risk factors for developing PPD are known, simple and inexpensive interventions to prevent PPD need to be studied. Postpartum mothers will be recruited for the study and randomized into control versus intervention group. The intervention group will be placed in a peer discussion group. Incidence of PPD will be tracked.

Publications & conference data

No peer-reviewed publications indexed yet for this trial. Completed trials usually publish results within 12-18 months.

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Other recruiting trials for Postpartum Depression

Currently open trials in the same condition.

Other Milton S. Hershey Medical Center trials

Trials by the same sponsor.

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Data sources for this page

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/NCT03793569.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing