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NCT01238614 Clinical Trial

Universal Screening for Maternal Depression With the CHICA System

Maternal Depression Clinical Trial

Official title:
Universal Screening for Maternal Depression With the CHICA System

Clinical Trial Details — Status: Completed

Administrative data
NCT number NCT01238614
Other study ID # MLM-CHICA-K-MD
Secondary ID K22LM009160
Status Completed
Phase N/A
First received November 9, 2010
Last updated November 9, 2010
Start date October 2007
Est. completion date September 2010

Study information
Verified date November 2010
Source Indiana University
Contact n/a
Is FDA regulated No
Health authority United States: Federal Government
Study type Interventional

Clinical Trial Summary

The CHICA system is a clinical decision support system that uses adaptive turnaround documents to provide point-of-care information to clinicians. We will be studying whether it can help in the diagnosis and referral of mothers with maternal depression.

Recruitment information / eligibility
Status Completed
Enrollment 3250
Est. completion date September 2010
Est. primary completion date July 2009
Accepts healthy volunteers No
Gender Female
Age group N/A and older
Eligibility Inclusion Criteria:

- All families of patients age 0 to 15 months

Exclusion Criteria:

Study Design

Allocation: Randomized, Intervention Model: Factorial Assignment, Masking: Single Blind (Outcomes Assessor), Primary Purpose: Screening

Related Conditions & MeSH terms

Intervention

Other:
• CHICA PSF plus JIT

• CHICA maternal depression PSF

• Control

Locations
Country Name City State
United States CHSR Indianapolis Indiana

Sponsors (2)
Lead Sponsor Collaborator
Indiana University National Library of Medicine (NLM)

Country where clinical trial is conducted

United States, 

Outcome
Type Measure Description Time frame Safety issue
Primary Percent of mothers screening positive for maternal depression. 1 year after child's birth No
Secondary Percent of mothers diagnosed with maternal depression one year after child's birth No
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