Universal Screening for Maternal Depression With the CHICA System

NCT ID: NCT01238614

Last Updated: 2010-11-10

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.

Recruitment Status

COMPLETED

Clinical Phase

NA

Total Enrollment

3250 participants

Study Classification

INTERVENTIONAL

Study Start Date

2007-10-31

Study Completion Date

2010-09-30

Brief Summary

Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.

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.

Detailed Description

Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.

Conditions

See the medical conditions and disease areas that this research is targeting or investigating.

Maternal Depression

Keywords

Explore important study keywords that can help with search, categorization, and topic discovery.

maternal depression clinical decision support

Study Design

Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.

Allocation Method

RANDOMIZED

Intervention Model

FACTORIAL

Primary Study Purpose

SCREENING

Blinding Strategy

SINGLE

Outcome Assessors

Study Groups

Review each arm or cohort in the study, along with the interventions and objectives associated with them.

PSF-JIT

Mothers in this arm receive prescreening questions and clinicians receive just-in-time handouts to aid in diagnosis.

Group Type EXPERIMENTAL

CHICA PSF plus JIT

Intervention Type OTHER

PSF

Mothers in this arm receive screening questions on the prescreener form

Group Type EXPERIMENTAL

CHICA maternal depression PSF

Intervention Type OTHER

Control

Mothers in this arm receive no maternal depression CHICA additional care

Group Type PLACEBO_COMPARATOR

Control

Intervention Type OTHER

Interventions

Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.

CHICA PSF plus JIT

Intervention Type OTHER

CHICA maternal depression PSF

Intervention Type OTHER

Control

Intervention Type OTHER

Eligibility Criteria

Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.

Inclusion Criteria

* All families of patients age 0 to 15 months

Exclusion Criteria

* None
Eligible Sex

FEMALE

Accepts Healthy Volunteers

No

Sponsors

Meet the organizations funding or collaborating on the study and learn about their roles.

National Library of Medicine (NLM)

NIH

Sponsor Role collaborator

Indiana University

OTHER

Sponsor Role lead

Responsible Party

Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.

IUPUI

Locations

Explore where the study is taking place and check the recruitment status at each participating site.

CHSR

Indianapolis, Indiana, United States

Site Status

Countries

Review the countries where the study has at least one active or historical site.

United States

Other Identifiers

Review additional registry numbers or institutional identifiers associated with this trial.

K22LM009160

Identifier Type: NIH

Identifier Source: secondary_id

View Link

MLM-CHICA-K-MD

Identifier Type: -

Identifier Source: org_study_id