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NCT00055081 Clinical Trial

The Impact of Family CTI on Homeless Children

Mental Health Clinical Trial

Official title:
The Impact of Family CTI on Homeless Children

Clinical Trial Details — Status: Completed

Administrative data
NCT number NCT00055081
Other study ID # R01MH067148
Secondary ID R01MH067148DSIR
Status Completed
Phase N/A
First received February 19, 2003
Last updated December 5, 2013
Start date July 2002
Est. completion date November 2005

Study information
Verified date December 2013
Source Nathan Kline Institute for Psychiatric Research
Contact n/a
Is FDA regulated No
Health authority United States: Federal Government
Study type Interventional

Clinical Trial Summary

The purpose of this study is to examine how services and housing provided for homeless families affect the mental health and behavior of homeless children over time.

Description:

This study is a supplement to a parent study which concentrates on the outcomes of homeless mothers who are provided with services and housing. This study will focus on the effects of housing and services on children, who may be the major beneficiaries of such assistance.

Participants are randomly assigned to either receive services and permanent housing or to remain in a homeless shelter without additional assistance. Children and their parents are interviewed separately 3, 9, and 15 months after study entry. The teachers of participating children are surveyed twice during the study.

Recruitment information / eligibility
Status Completed
Enrollment 320
Est. completion date November 2005
Est. primary completion date November 2005
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Both
Age group 18 Months to 16 Years
Eligibility Inclusion Criteria:

- Enrollment in the parent study

- Homeless and living at a shelter with mother/maternal guardian at the time of study enrollment

Study Design

Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Treatment

Related Conditions & MeSH terms

Intervention

Behavioral:
• Critical Time Intervention

Locations
Country Name City State
United States The Nathan S. Kline Institute for Psychiatric Research Orangeburg New York

Sponsors (2)
Lead Sponsor Collaborator
Nathan Kline Institute for Psychiatric Research National Institute of Mental Health (NIMH)

Country where clinical trial is conducted

United States, 

Outcome
Type Measure Description Time frame Safety issue
Primary Internalizing, externalizing, school outcomes 18 months post enrollment No
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