Universal Screening for Maternal Depression With the CHICA System
This study has been completed.
Sponsor:
Indiana University
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
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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| Ages Eligible for Study: | Child, Adult, Senior |
| Genders 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
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 |
| 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 27, 2016