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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

Trial Contacts

ContactsICMJE

Contact information is displayed when a study is open for participants to join.

Study Record Dates

First SubmittedICMJENot provided
First PostedICMJE

2026-01-12

Last Update Posted

2026-06-12

Last Verified*

2026-06

Outcome Measures

Primary Outcome Measures*ICMJE

Incidence of postnatal depression [Time Frame: Within 6 weeks of delivery]

Secondary Outcome Measures[*]ICMJE

Sensitivity and specificity of routine screening [Time Frame: 6 weeks]

Other Pre-specified Outcome MeasuresNot provided

See all versions of this study

Trial Description

Brief Title*ICMJE

Postnatal Depression Screening in Primary Health Centres

Official Title*§ICMJE

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

Acronym[*]Not provided
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.

Study Type*ICMJE

Observational

Study Phase*ICMJENot provided
Study Design*§ICMJE

Observational Model: Cohort

Time Perspective: Prospective

Patient Registry

No

BiospecimenNot provided
Sampling Method*Not provided
Study Population*Not provided
Condition*ICMJE

Postnatal Depression

Keywords

postnatal depression

screening

maternal mental health

Intervention*ICMJENot provided
Study Groups/Cohorts*ICMJENot provided
PublicationsNot provided

Recruitment Information

Recruitment Status*ICMJE

Active, not recruiting

Enrollment (Anticipated)*§ICMJE

1500

Study Start Date*§ICMJE

2026-01-15

Primary Completion Date*

2026-12-31 (Final data collection date for primary outcome measure)

Study Completion Date*§ICMJE

2027-03-31

Eligibility Criteria*ICMJE

<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>

Sex/Gender*ICMJE

Sexes Eligible for Study: Female

Ages*ICMJE

18 Years to 45 Years (Adult)

Accepts Healthy Volunteers*§ICMJE

No

Location CountriesICMJE

Bangladesh

Administrative Information

BDCTR NumberICMJE

BDCTR-2026-000057

Other Study ID Numbers[*]ICMJE

BMU-PSY-2026-001

Has Data Monitoring Committee

No

Studies a U.S. FDA-regulated Drug ProductNot provided
Studies a U.S. FDA-regulated Device ProductNot provided
Device Product Not Approved or Cleared by U.S. FDANot provided
Pediatric Postmarket Surveillance of a Device ProductNot provided
Product Manufactured in and Exported from the U.S.Not provided
IPD Sharing StatementICMJE

Plan to Share IPD: Not provided

Current Responsible Party*

Dr Sabrina Yeasmin

Current Study Sponsor*ICMJE

Bangladesh Medical University

CollaboratorsICMJENot provided
InvestigatorsICMJENot provided
Registry Account

Imported legacy public registry

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*
Required
*§
Required if Study Start Date is on or after January 18, 2017 — required for every BMU study
[*]
Conditionally required
No Symbol
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ICMJE
Data element required by the International Committee of Medical Journal Editors and the World Health Organization ICTRP