Tailored Teen Alcohol and Violence Prevention in the Emergency Room (ER)
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Purpose
This study is designed to address both alcohol misuse and violence among adolescents ages 14-18 seeking care in an urban emergency department (ED). The study is a randomized controlled trial comparing the effectiveness of a combined Adapted Motivational Interviewing and Skills Training intervention, delivered either by a computer or by a counselor, and an informational handout control condition.
| Condition | Intervention |
|---|---|
|
Violence Alcohol Abuse |
Behavioral: Adapted Motivational Interviewing & Skills Training |
| Study Type: | Interventional |
| Study Design: | Allocation: Randomized Endpoint Classification: Efficacy Study Intervention Model: Factorial Assignment Masking: Single Blind (Outcomes Assessor) Primary Purpose: Prevention |
| Official Title: | Tailored Teen Alcohol and Violence Prevention in the ER |
- Primary outcome variables include alcohol misuse and violent behaviors. [ Time Frame: 12-months ] [ Designated as safety issue: Yes ]
- Secondary outcome measures include illicit drug use, unintentional injury, delinquency and weapon carriage. [ Time Frame: 12-months ] [ Designated as safety issue: Yes ]
| Estimated Enrollment: | 3000 |
| Study Start Date: | September 2006 |
| Estimated Study Completion Date: | October 2013 |
| Primary Completion Date: | October 2010 (Final data collection date for primary outcome measure) |
| Arms | Assigned Interventions |
|---|---|
|
Active Comparator: 1
Therapist delivered adapted motivational enhancement therapy and skills training
|
Behavioral: Adapted Motivational Interviewing & Skills Training
Single session, 45 minute brief intervention during Emergency Department Visit
Other Names:
|
|
Active Comparator: 2
Computer delivered adapted motivational enhancement therapy and skills training
|
Behavioral: Adapted Motivational Interviewing & Skills Training
Single session, 45 minute brief intervention during Emergency Department Visit
Other Names:
|
|
No Intervention: 3
3: Control brochure
|
Detailed Description:
This study will screen ~3000 adolescents in the ED (ages 14-18) over 30 months. Eligible adolescents will be asked to participate in the longitudinal study, stratified by age and gender and randomized to conditions (n=225/group): Computer Prevention Program, Counselor Prevention Program, or an informational handout control condition. Primary outcomes will be evaluated at 3, 6 and 12-months and include alcohol use/misuse, violent behaviors, illicit drug use, unintentional injury, delinquency, and weapon carriage. The proposed study integrates brief intervention strategies for alcohol misuse and violent behaviors using state-of-the-art technology to tailor the interventions to the specific risk factors of the adolescent. Tailored computerized programs use available technology to replace the need for clinical staff in the ED setting, where there is limited staff time to effect behavior change. This project will provide the critical first step toward the implementation of an integrated prevention program addressing overlapping risk factors that has the potential to be delivered to the millions of adolescents visiting urban Emergency Departments each year.
Eligibility| Ages Eligible for Study: | 14 Years to 18 Years |
| Genders Eligible for Study: | Both |
| Accepts Healthy Volunteers: | No |
Inclusion Criteria:
- adolescents (ages 14-18) presenting to the ED for a medical injury or illness (except exclusions as noted below)
- adolescents ability to provide informed assent/consent depending on age
- access to a parent or guardian to provide informed consent
Exclusion Criteria:
- adolescents who do not understand English
- prisoners
- adolescents classified by medical staff as "Level 1" trauma
- adolescents deemed unable to provide informed consent
- adolescents treated in the ED for suicide attempts
- adolescents triaged to the psychiatric ED
Contacts and Locations
More Information
Publications:
Additional publications automatically indexed to this study by ClinicalTrials.gov Identifier (NCT Number):
| Responsible Party: | Maureen A Walton, Professor, University of Michigan |
| ClinicalTrials.gov Identifier: | NCT00251212 History of Changes |
| Other Study ID Numbers: | AA-014889-01A1 |
| Study First Received: | November 7, 2005 |
| Last Updated: | October 9, 2012 |
| Health Authority: | United States: Institutional Review Board |
Keywords provided by University of Michigan:
|
Alcohol Violence Alcohol consumption Alcohol, drinking |
Additional relevant MeSH terms:
|
Alcoholism Alcohol-Related Disorders Substance-Related Disorders Mental Disorders |
ClinicalTrials.gov processed this record on May 23, 2013