Viewing Study NCT00251342



Ignite Creation Date: 2024-05-05 @ 12:07 PM
Last Modification Date: 2024-10-26 @ 9:20 AM
Study NCT ID: NCT00251342
Status: UNKNOWN
Last Update Posted: 2007-04-05
First Post: 2005-11-09

Brief Title: Outcome of Postnatal Depression Screening Using Edinburgh Postnatal Depression Scale
Sponsor: Chinese University of Hong Kong
Organization: Chinese University of Hong Kong

Study Overview

Official Title: Outcome of Postnatal Depression Screening Using Edinburgh Postnatal Depression Scale
Status: UNKNOWN
Status Verified Date: 2007-04
Last Known Status: RECRUITING
Delayed Posting: No
If Stopped, Why?: Not Stopped
Has Expanded Access: False
If Expanded Access, NCT#: N/A
Has Expanded Access, NCT# Status: N/A
Acronym: None
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: None

Study Oversight

Has Oversight DMC: None
Is a FDA Regulated Drug?: None
Is a FDA Regulated Device?: None
Is an Unapproved Device?: None
Is a PPSD?: None
Is a US Export?: None
Is an FDA AA801 Violation?: None
Secondary IDs
Secondary ID Type Domain Link
CUHK_CCT00019 None None None