Universal Screening for Maternal Depression With the CHICA System

This study has been completed.
Sponsor:
Collaborator:
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 Blind (Outcomes Assessor)
Primary Purpose: Screening
Official Title: Universal Screening for Maternal Depression With the CHICA System

Resource links provided by NLM:


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 ] [ Designated as safety issue: No ]

Secondary Outcome Measures:
  • Percent of mothers diagnosed with maternal depression [ Time Frame: one year after child's birth ] [ Designated as safety issue: No ]

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

Genders Eligible for Study:   Female
Accepts Healthy Volunteers:   No
Criteria

Inclusion Criteria:

  • All families of patients age 0 to 15 months

Exclusion Criteria:

  • None
  Contacts and Locations
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
  More Information

No publications provided

Responsible Party: Paul Biondich, IUPUI
ClinicalTrials.gov Identifier: NCT01238614     History of Changes
Other Study ID Numbers: MLM-CHICA-K-MD, K22LM009160
Study First Received: November 9, 2010
Last Updated: November 9, 2010
Health Authority: United States: Federal Government

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 April 17, 2014