Outcome of Postnatal Depression Screening Using Edinburgh Postnatal Depression Scale

Phase 2

• Conditions: Depression, Postpartum

• Registration Number: NCT00251342
• Lead Sponsor: Chinese University of Hong Kong

Brief Summary

The objective of the present study is to evaluate the effectiveness of postnatal depression screening by comparing the mental health outcome (at 6 months postpartum) of mothers under the Edinburgh Postnatal Depression Scale (EPDS) screening programme versus usual clinical practice (usual practice), using randomized controlled trial design. With the use of the EPDS for the screening of postnatal depression, it is expected that more mothers in need of intervention (including mental health intervention, guidance in childcare and parenting, counseling in family relationships, etc) will be picked up and offered appropriate intervention, compared to the usual practice. It is hypothesized that the mental health of the group of women under the EPDS screening programme will be better than those under the usual practice, on subsequent follow-up.

Detailed Description

Not available

Study Timeline

• Study Start: 2005-10
• Study First Submitted: 2005-11-09
• Study First Submitted QC: 2005-11-09
• Study First Posted: 2005-11-10
• Status Verified: 2007-04
• Last Update Submitted: 2007-04-04
• Last Update Posted: 2007-04-05
• Study Completion: 2008-01

Recruitment & Eligibility

• Status: UNKNOWN
• Sex: Female
• Target Recruitment: 460

Inclusion Criteria

1. Chinese mothers of newborn babies <= 2 months who are registered with the 4 Maternal and Child Health Centres under study;
2. Normally resident in Hong Kong (Hong Kong ID card holder, or HK Birth Certificate [with status of permanent resident indicated established] holder, or people who have been granted unconditional stay in Hong Kong, or passport holders having valid travel document showing the right to land in Hong Kong, or permission to land, or eligibility of HK permanent ID card verified, or entitlement to the right of abode in HK)

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Exclusion Criteria

1. Those who do not use the Chinese language (in both the written and spoken form);
2. Those who are under active psychiatric contact;
3. Those who delivered in hospitals which are still conducting their own EPDS screening programme.

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Study & Design

• Study Type: INTERVENTIONAL
• Study Design: PARALLEL

Primary Outcome Measures

Name	Time	Method
Mother's mental health at 6 months postpartum, as measured on the EPDS and General Health Questionnaire-12 (GHQ-12), both being self-report questionnaires.

Secondary Outcome Measures

Name	Time	Method
Mother's parenting stress (measured by the Parenting Stress Index, a self-report questionnaire)
Marital relationship satisfaction (measured by the Chinese Kansas Marital Satisfaction Scale, a self-report questionnaire)
Marital status and employment status (both father and mother, where applicable) at 6 and 18 months postpartum
Child health measures, including weight at 6 and 18 months, number of hospitalizations and visits to doctors within the first 6 and 18 months as reported by mother
Mother's mental health outcome (EPDS and GHQ scores) at 18 months postpartum

Trial Locations

Locations (1)

Maternal and Child Health Centres, Department of Health; 🇨🇳 Hong Kong, China