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Postnatal Depression Screening in Primary Health Centres

BDCTR ID
BDCTR-2026-000057
Sponsor
Bangladesh Medical University
Information provided by
Dr Sabrina Yeasmin (Responsible Party)
Last Update Posted
2026-06-12

Active, not recruiting

No longer looking for participants

Study Overview

Brief Summary

This observational cohort estimates the incidence of postnatal depression and the performance of routine screening in primary health centres.

Detailed Description

Women are followed from delivery to six weeks postpartum with routine screening. Incidence and screening performance are assessed.

Official Title

A Prospective Cohort of Postnatal Depression Incidence and Screening Performance in Primary Health Centres

Conditions

  • Postnatal Depression

Other Study ID Numbers

BMU-PSY-2026-001

Study Start

2026-01-15

Primary Completion

2026-12-31

Study Completion

2027-03-31

Enrollment (Estimated)

1,500

Study Type

Observational

Phase

Not Applicable

Resource links provided by the National Library of Medicine

Contacts and Locations

This section provides contact details for people who can answer questions about joining this study, and information on where this study is taking place.

To learn more, please see the Contacts and Locations section in How to Read a Study Record.

This study has 1 location

Bangladesh

  • Khulna, Khulna, Bangladesh, 9000

    Active, not recruiting

    Primary health centres, Khulna

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

For general information about clinical research, read Learn About Studies.

Eligibility Criteria

<p>Inclusion Criteria:</p><ul><li>Women aged 18 to 45 years who have given birth at a participating centre.</li></ul><p>Exclusion Criteria:</p><ul><li>Diagnosed depression before pregnancy.</li></ul>

Ages Eligible for Study

18 Years to 45 Years (Adult)

Sexes Eligible for Study

Female

Accepts Healthy Volunteers

No

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

Observational Model:
Cohort
Time Perspective:
Prospective

What is the study measuring?

Primary Outcome Measures

Outcome MeasureMeasure DescriptionTime Frame
Incidence of postnatal depressionWithin 6 weeks of delivery

Secondary Outcome Measures

Outcome MeasureMeasure DescriptionTime Frame
Sensitivity and specificity of routine screening6 weeks

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Sponsor

Bangladesh Medical University

Study Record Dates

These dates track the progress of study record and summary results submissions to the registry. Study records and reported results are reviewed by the Registry Office to make sure they meet specific quality control standards before being posted on the public website.

Study Registration Dates

First Submitted that Met QC Criteria

2026-01-12

First Posted

2026-01-12

Study Record Updates

Last Update Submitted that Met QC Criteria

2026-06-12

Last Update Posted

2026-06-12

Last Verified

2026-06

More Information

Record History

Terms related to this study

Keywords Provided by Bangladesh Medical University

  • postnatal depression
  • screening
  • maternal mental health

Plan for Individual Participant Data (IPD)

Plan to Share Individual Participant Data (IPD)?

Not provided

Drug and device information, study documents, and helpful links

Data Monitoring Committee

No
Postnatal Depression Screening in Primary Health Centres (BDCTR-2026-000057) | BMU Clinical Trial Registry