- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT01616212
Early Intervention for Minors in Possession of Alcohol/Drugs: A Feasibility Study (MAST1)
The purpose of this study is to evaluate two brief, sustainable interventions for a sample of 280 adolescents charged with an initial drug-related offense: Motivational Enhancement Therapy (MET) intervention for youth and the Parenting Wisely (PW) intervention for parents. Families are assessed for adolescent substance use, HIV-risk, recidivist substance-related offenses, treatment entry, and other areas of individual and family functioning.
It is expected that the combined MET+PW interventions will be more effective than a treatment-as-usual intervention (drug education group) for adolescents with parents not participating in PW.
Study Overview
Status
Conditions
Detailed Description
Illicit substance use and related problems among adolescents has been consistently high over the past decade and remains one of the most pressing public health concerns in the United States. The objective of this study is to conduct a pilot investigation of the feasibility and effectiveness of two brief empirically based treatments for adolescent substance abuse when implemented as early interventions for youth arrested and charged with first- or second-offense possession of alcohol or drugs. The two examined interventions are Motivational Enhancement therapy (MET) and Parenting Wisely (PW).
Over a one-year period, 280 adolescents and their parents will be referred to the study by the Juvenile Justice Centers in two Oregon counties within the Portland metro area. Families will be randomized to one of four intervention conditions; youth will receive either MET or a drug education intervention (EDUC), and the PW intervention for parents is present or absent. Participants will be assessed for adolescent substance use, HIV-risk, recidivist substance-related offenses, treatment entry, and other areas of individual and family functioning at intake and at 3- and 6-month follow-ups.
Study Type
Enrollment (Actual)
Phase
- Phase 1
Contacts and Locations
Study Locations
-
-
Oregon
-
Portland, Oregon, United States, 97232
- Oregon Research Institute
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Description
Inclusion Criteria:
- 13 - 17 years of age
- Referral for a 1st or 2nd Minor in Possession (Alcohol) or Less Than an Ounce (Marijuana) offense
- Adolescents living at home with at least one parent willing to participate in the study
- Adolescents with sufficient English-language ability to permit participation in the interventions
- Parent(s) with sufficient English- or Spanish-language ability to complete the English- or Spanish-language versions of PW and the assessment
Exclusion Criteria:
- Evidence of psychotic or organic state of sufficient severity to interfere with understanding study procedures
- Danger to self and/or services other than outpatient treatment are required
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Treatment
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
---|---|
Experimental: TX1
Motivational Enhancement Therapy for adolescents, Parenting Wisely for parents
|
Motivational Enhancement Therapy for adolescents, Parenting Wisely for parents
Other Names:
|
Experimental: TX 2
Motivational Enhancement Therapy for adolescents
|
Motivational Enhancement Therapy for adolescents
Other Names:
|
Experimental: TX3
Drug Education for adolescents, Parenting Wisely for parents
|
Drug Education for adolescents, Parenting Wisely for parents
Other Names:
|
Experimental: TX4
Drug Education for adolescents
|
Drug Education for adolescents
Other Names:
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Adolescent Substance Use and Related Problems
Time Frame: Change from Baseline at 6 months
|
The questionnaire used is called the Time Line Follow Back.
|
Change from Baseline at 6 months
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Dysfunctional Discipline Practices
Time Frame: Change from Baseline at 6 months
|
The questionnaire used to obtain this information is called Parenting Scale.
|
Change from Baseline at 6 months
|
Collaborators and Investigators
Sponsor
Investigators
- Principal Investigator: Hyman Hops, Ph.D., Oregon Research Institute
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
- DA-12-033
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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