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Universal Screening for Maternal Depression With the CHICA System

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ClinicalTrials.gov Identifier: NCT01238614
Recruitment Status : Completed
First Posted : November 10, 2010
Last Update Posted : November 10, 2010
Sponsor:
Collaborator:
Information provided by:

Study Description
Brief 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.

Condition or disease Intervention/treatment
Maternal Depression Other: CHICA PSF plus JIT Other: CHICA maternal depression PSF Other: Control

Study Design

Study Type : Interventional  (Clinical Trial)
Actual Enrollment : 3250 participants
Allocation: Randomized
Intervention Model: Factorial Assignment
Masking: Single (Outcomes Assessor)
Primary Purpose: Screening
Official Title: Universal Screening for Maternal Depression With the CHICA System
Study Start Date : October 2007
Primary Completion Date : July 2009
Study Completion Date : September 2010
Arms and Interventions

Arm Intervention/treatment
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


Outcome Measures

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

Secondary Outcome Measures :
  1. Percent of mothers diagnosed with maternal depression [ Time Frame: one year after child's birth ]

Eligibility Criteria

Information from the National Library of Medicine

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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

Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its ClinicalTrials.gov identifier (NCT number): 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 )
First Posted: November 10, 2010    Key Record Dates
Last Update Posted: November 10, 2010
Last Verified: November 2010

Keywords provided by Indiana University:
maternal depression
clinical decision support

Additional relevant MeSH terms:
Depression
Depressive Disorder
Behavioral Symptoms
Mood Disorders
Mental Disorders