Universal Screening for Maternal Depression With the CHICA System

This study has been completed.

Sponsor:

Collaborator:

National Library of Medicine (NLM)

Information provided by:

Indiana University

ClinicalTrials.gov Identifier:

NCT01238614

First received: November 9, 2010

Last updated: NA

Last verified: November 2010

History: No changes posted

Purpose

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.

Condition	Intervention
Maternal Depression	Other: CHICA PSF plus JIT Other: CHICA maternal depression PSF Other: Control


Study Type:	Interventional
Study Design:	Allocation: Randomized Intervention Model: Factorial Assignment Masking: Single (Outcomes Assessor) Primary Purpose: Screening
Official Title:	Universal Screening for Maternal Depression With the CHICA System

Further study details as provided by Indiana University:

Primary Outcome Measures:

Percent of mothers screening positive for maternal depression. [ Time Frame: 1 year after child's birth ]

Secondary Outcome Measures:

Percent of mothers diagnosed with maternal depression [ Time Frame: one year after child's birth ]


Enrollment:	3250
Study Start Date:	October 2007
Study Completion Date:	September 2010
Primary Completion Date:	July 2009 (Final data collection date for primary outcome measure)

Arms	Assigned Interventions
Experimental: PSF-JIT Mothers in this arm receive prescreening questions and clinicians receive just-in-time handouts to aid in diagnosis.	Other: CHICA PSF plus JIT
Experimental: PSF Mothers in this arm receive screening questions on the prescreener form	Other: CHICA maternal depression PSF
Placebo Comparator: Control Mothers in this arm receive no maternal depression CHICA additional care	Other: Control

Eligibility


Ages Eligible for Study:	Child, Adult, Senior
Sexes Eligible for Study:	Female
Accepts Healthy Volunteers:	No

Criteria

Inclusion Criteria:

All families of patients age 0 to 15 months

Exclusion Criteria:

Contacts and Locations

Choosing to participate in a study is an important personal decision. Talk with your doctor and family members or friends about deciding to join a study. To learn more about this study, you or your doctor may contact the study research staff using the Contacts provided below. For general information, see Learn About Clinical Studies.

Please refer to this study by its ClinicalTrials.gov identifier: NCT01238614

Locations


United States, Indiana
CHSR
Indianapolis, Indiana, United States, 46202

Sponsors and Collaborators

Indiana University

National Library of Medicine (NLM)

More Information


Responsible Party:	Paul Biondich, IUPUI
ClinicalTrials.gov Identifier:	NCT01238614 History of Changes
Other Study ID Numbers:	MLM-CHICA-K-MD K22LM009160 ( U.S. NIH Grant/Contract )
Study First Received:	November 9, 2010
Last Updated:	November 9, 2010

Keywords provided by Indiana University:


maternal depression clinical decision support

Additional relevant MeSH terms:


Depression Depressive Disorder Behavioral Symptoms Mood Disorders Mental Disorders

ClinicalTrials.gov processed this record on August 18, 2017

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