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NCT06770244

Positive Psychology-Based Intervention Program for Postpartum Depression Within Primary Healthcare System

ENROLLING BY INVITATION NA Last updated 21 February 2025
What this trial tests

NA trial testing positive psychology-based intervention package in Postpartum Depression (PPD) in 1,438 participants. Enrolling by invitation.

Timeline
1 February 2025
Primary endpoint
1 May 2026
31 October 2026

Quick facts

Lead sponsorHuazhong University of Science and Technology
PhaseNA
StatusENROLLING BY INVITATION
Study typeINTERVENTIONAL
Allocationrandomized
Designparallel
Maskingsingle
Primary purposeprevention
Enrollment1,438
Start date1 February 2025
Primary completion1 May 2026
Estimated completion31 October 2026
Sites1 location across China

Drugs / interventions tested

Conditions studied

Sponsor

Huazhong University of Science and Technology

Who can join

18 and older, female only, with Postpartum Depression (PPD). Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

This study is a prospective, two-arm parallel cluster randomized controlled trial that will compare the intervention effects of a positive psychology-based intervention package with usual care for postpartum depression.

Publications & conference data

1 peer-reviewed publication reference this trial (live from Europe PMC):

  1. Positive psychology-based intervention programme for postpartum depression among pregnant women within the primary healthcare system: protocol for a randomised controlled trial.
    Fan Z, Weng M, Su J, Yu R, et al · · 2025 · PMID 40780718 · DOI 10.1136/bmjopen-2025-101115

Verify or expand the search:

Other recruiting trials for Postpartum Depression (PPD)

Currently open trials in the same condition.

Other Huazhong University of Science and Technology trials

Trials by the same sponsor.

Verify against primary sources

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/NCT06770244.

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