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

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
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
  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 September 30, 2014