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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 Record Versions

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Viewing V1 (2026-06-12)

Study Details

Study Identification

Unique Protocol IDBMU-PSY-2026-001
Brief TitlePostnatal Depression Screening in Primary Health Centres
Official TitleA Prospective Cohort of Postnatal Depression Incidence and Screening Performance in Primary Health Centres
Secondary IDs

Study Status

Record Verification2026-06
Overall StatusActive, not recruiting
Study Start2026-01-15
Primary Completion2026-12-31
Study Completion2027-03-31
First Submitted
First Submitted that Met QC Criteria2026-01-12
First Posted2026-01-12 [Actual]
Last Update Submitted that Met QC Criteria2026-06-12
Last Update Posted2026-06-12 [Actual]

Oversight

U.S. FDA-regulated Drug
U.S. FDA-regulated Device
Product manufactured in and exported from the U.S.
Data MonitoringNo

Study Description

Brief SummaryThis observational cohort estimates the incidence of postnatal depression and the performance of routine screening in primary health centres.
Detailed DescriptionWomen are followed from delivery to six weeks postpartum with routine screening. Incidence and screening performance are assessed.

Conditions

ConditionPostnatal Depression
Keywordspostnatal depression screening maternal mental health

Study Design

Study TypeObservational
Patient RegistryNo
Observational Study ModelCohort
Time PerspectiveProspective
Biospecimen Retention
Biospecimen Description
Enrollment1500 [Estimated]

Arms and Interventions

Groups/CohortsInterventions

Outcome Measures

Primary Outcome MeasuresIncidence of postnatal depression Time Frame: Within 6 weeks of delivery
Secondary Outcome MeasuresSensitivity and specificity of routine screening Time Frame: 6 weeks

Eligibility

Minimum Age18 Years
Maximum Age45 Years
Ages18 Years to 45 Years (Adult)
SexFemale
Gender-based Eligibility
Gender Eligibility Description
Accepts Healthy VolunteersNo
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>
Study Population
Sampling Method

Contacts/Locations

Central Contact PersonDr Sabrina Yeasmin pnd-screen@bmu.ac.bd
Study Officials
LocationKhulna, Khulna, Bangladesh, 9000 Status: Active, not recruiting Facility: Primary health centres, Khulna

IPD Sharing

IPD informationPlan to Share IPD: Not provided

References

Citations
Links
Available IPD/Information

Document Section

Documents