- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT01948700
Assessing the Fit of Motivational Interviewing by Cultures With Adolescents (AMICA)
March 9, 2024 updated by: University of New Mexico
AMICA: Assessing the Fit of Motivational Interviewing by Cultures With Adolescents
Hispanic adolescents experience more severe alcohol-related consequences due to their alcohol abuse and yet significantly fewer Hispanic adolescents receive alcohol treatment, particularly among justice-involved youth.
Despite the level of research that has been conducted on motivational interviewing (MI) with mainstream samples, no published studies have investigated the efficacy of this brief, individual intervention with Hispanic adolescents.
The overarching objective of this application is to evaluate the efficacy of a brief individual intervention (MI) for problem drinking behaviors with a sample of justice-involved Hispanic and Caucasian adolescents to determine if this intervention is differentially effective between Hispanic and Caucasian adolescents.
Specifically, the first aim is to determine whether an MI intervention targeting alcohol abuse is effective at reducing alcohol use and related risk behavior in a sample of adolescent alcohol abusers.
The second aim is to examine whether the effects of MI on problem drinking outcomes (e.g., alcohol problems, quantity of drinking, frequency of binging) are different between Hispanic versus Caucasian adolescents.
Because it is important to determine the mechanisms that mediate the effects of MI and determine whether these mechanisms differ between Caucasian and Hispanic adolescents, the third aim is to examine whether group (Hispanic vs. Caucasian) moderates the mediational linkages in the overall model using a cross-groups approach to moderated mediation.
To accomplish these aims, 453 Caucasian and Hispanic justice-involved alcohol abusing adolescents (ages 14-17) will be randomized to either two 60 minute MI interventions (one at baseline and a second, one week later) or an education condition.
All adolescents will receive behavioral assessments at baseline, 3, 6 and 12 months.
The proposed research is expected to take a significant step towards reducing current racial/ethnic health disparities in alcohol treatment for Hispanic adolescents.
Study Overview
Status
Terminated
Conditions
Intervention / Treatment
Study Type
Interventional
Enrollment (Actual)
506
Phase
- Not Applicable
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
-
-
New Mexico
-
Albuquerque, New Mexico, United States, 87106
- University of New Mexico Center on Alcoholism, Substance Abuse, and Addictions
-
-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
13 years to 18 years (Child, Adult)
Accepts Healthy Volunteers
No
Description
Inclusion Criteria:
- Age 13 - 18
- Provision of informed assent (or self-consent if age 18)
- Parent/ guardian consent if under age 18
- Regular substance use (use at least 1 per month for past 6 months)
Exclusion Criteria:
- active psychosis
- mental retardation
- neurodevelopmental disorder
- severe medical illness
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Primary Purpose: Prevention
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Single
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Other: Brief Intervention
Motivational Interviewing (MI)
|
|
|
Other: Standard Intervention
Education
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Time Frame |
|---|---|
|
Frequency of alcohol use
Time Frame: Change from baseline in frequency of alcohol use at 3 , 6 , & 12 month follow-up
|
Change from baseline in frequency of alcohol use at 3 , 6 , & 12 month follow-up
|
Secondary Outcome Measures
Outcome Measure |
Time Frame |
|---|---|
|
Quantity of alcohol use
Time Frame: Change from baseline in quantity of alcohol use at 3 , 6 , & 12 month follow-up
|
Change from baseline in quantity of alcohol use at 3 , 6 , & 12 month follow-up
|
Other Outcome Measures
Outcome Measure |
Time Frame |
|---|---|
|
Number of alcohol-related problems as indicated in the Rutgers Alcohol Problems Index
Time Frame: Change from baseline in number of alcohol-related problems at 3 , 6 , & 12 month follow-up
|
Change from baseline in number of alcohol-related problems at 3 , 6 , & 12 month follow-up
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Collaborators
Investigators
- Principal Investigator: Sarah W. Feldstein Ewing, Ph. D., Assistant Professor UNM
Publications and helpful links
The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (Actual)
October 1, 2009
Primary Completion (Actual)
July 1, 2015
Study Completion (Actual)
July 1, 2015
Study Registration Dates
First Submitted
September 16, 2013
First Submitted That Met QC Criteria
September 18, 2013
First Posted (Estimated)
September 24, 2013
Study Record Updates
Last Update Posted (Actual)
March 12, 2024
Last Update Submitted That Met QC Criteria
March 9, 2024
Last Verified
March 1, 2024
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- 5R01AA017878-05 (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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