- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT01193114
Stage 1 Treatment Development With Homeless Mothers
Stage 1 Treatment Development With Homeless Mothers and Their 2-6 Year Old Children
Aim 1. Identify specific targets and processes of intervention among homeless substance abusing mothers with children between the ages of 2 and 6 years from information collected in focus groups and assessment interviews. Translate that information for the refinement of the ecologically based treatment manual.
Aim 2. Test the efficacy of the treatment in a nonrandomized pilot study and revise the manual based upon those findings.
Aim 3. Test the efficacy of the experimental intervention compared to treatment as usual (TAU) in a randomized pilot, with the goal to improve maternal substance abuse problems, social stability, and mental health. It is expected that the experimental intervention will be associated with lower substance use and related problem behaviors than TAU.
Aim 4. Test whether intended change processes (mediators) associated with the intervention produce the desired change in mother's substance use, social stability, and mental health. It is expected that self-efficacy will mediate substance use outcomes.
Aim 5. Explore how length of homelessness, age and ethnicity of the mother predict treatment response (moderators).
Aim 6. Explore the impact of the experimental intervention (Ecologically-Based Therapy)on interpersonal stress and child's mental health.
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
-
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Ohio
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Columbus, Ohio, United States, 43210
- The Ohio State University Department of Human Development and Family Science
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Description
Inclusion Criteria:
- residing at a homeless shelter for families
- meet diagnostic criteria for psychoactive substance use or alcohol disorder
- has physical custody of a biological child between the ages of 2 to 6 years old
Exclusion Criteria:
- evidence of unremitted psychosis or other condition that would impair the mothers' ability to understand and participate in the intervention research.
Study Plan
How is the study designed?
Design Details
- Primary Purpose: TREATMENT
- Allocation: RANDOMIZED
- Interventional Model: PARALLEL
- Masking: NONE
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Ecologically-Based Behavioral Treatment
Ecologically-Based Treatment was provided over a period of 6 months.
The treatment integrated independent housing, case management services and substance abuse counseling.
Specifically, the mothers were housed in an apartment of their choice and received three months of utility and rental assistance of up to $600 per month.
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Substance abuse treatment (the Community Reinforcement Approach), case management and housing.
|
|
Active Comparator: Treatment as Usual
The Mothers were offered services provided through the family shelter.
|
Treatment/intervention as normally provided by community service agencies that service substance abusing homeless families.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Time Frame |
|---|---|
|
Percent Days of Substance Use in the Prior 3 Months.
Time Frame: 3 months post-baseline measure
|
3 months post-baseline measure
|
|
Percent Days of Substance Use in the Prior 3 Months.
Time Frame: 6 months post-baseline measure
|
6 months post-baseline measure
|
|
Percent Days of Substance Use in the Prior 3 Months.
Time Frame: 9 months post-baseline measure
|
9 months post-baseline measure
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
BDI Depression Score
Time Frame: 3 months post-baseline measure
|
Beck Depression Inventory - II (BDI - II) Range from 0 (no depression) to 63 (severe depression)
|
3 months post-baseline measure
|
|
BDI Depression Score
Time Frame: 6 months post-baseline measure
|
Beck Depression Inventory - II (BDI - II) Range from 0 (no depression) to 63 (severe depression)
|
6 months post-baseline measure
|
|
BDI Depression Score
Time Frame: 9 months post-baseline measure
|
Beck Depression Inventory - II (BDI - II) Range from 0 (no depression) to 63 (severe depression)
|
9 months post-baseline measure
|
Collaborators and Investigators
Sponsor
Collaborators
Study record dates
Study Major Dates
Study Start
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Estimate)
Study Record Updates
Last Update Posted (Estimate)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- 2008B0309
- R01DA023908 (U.S. NIH Grant/Contract)
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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