Outcome of Postnatal Depression Screening Using Edinburgh Postnatal Depression Scale

The Chinese University of Hong Kong

Status and phase: Unknown; Phase 3; Phase 2

Conditions: Depression, Postpartum

Treatments: Procedure: Edinburgh Postnatal Depression Scale

Study type: Interventional

Funder types: Other

Identifiers

NCT00251342

CRE-2005.224-T

CUHK_CCT00019

Details and patient eligibility

About

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.

Sex: Female

Volunteers: Accepts Healthy Volunteers

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)

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.

Trial design

Primary purpose: Diagnostic

Allocation: Randomized

Interventional model: Parallel Assignment

Masking: Double Blind