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Trial of Computerized SBI to Reduce Teen Alcohol Use

Randomized Controlled Trial of Computerized SBI to Reduce Teen Alcohol Use

Status
Withdrawn
Phases
Phase 1
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01784627
Enrollment
0
Registered
2013-02-06
Start date
2015-01-31
Completion date
2017-10-31
Last updated
2016-10-07

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Alcohol Abuse, Cannabis Abuse, Nicotine Dependence

Keywords

substance use, alcohol abuse, cannabis abuse, nicotine dependence, adolescents

Brief summary

The goal of this project is to test the effectiveness of a computer-facilitated alcohol screening and brief intervention (c-ASBI) system for 12- to 18-year-old primary care patients in a multi-site, randomized comparative effectiveness trial. The investigators hypothesize that, among 12- to 18-year olds patients coming for annual well-care, those receiving c-ASBI will have lower rates of any alcohol use at 3-, 6-, and 12-month follow-ups compared to Treatment As Usual (TAU).

Detailed description

The Specific Aims are to 1) Test the effects of c-ASBI on any alcohol use; 2) Test the effects of c-ASBI separately as a prevention, therapeutic, and risk-reduction intervention; 3) Test the effects of c-ASBI separately on cannabis and tobacco use; explore its effects on other drug use; and 4) Assess potential moderators (e.g., age, gender, race/ethnicity, substance use history +/-, parent/sibling/peer substance use), mediators (e.g., Youth to Provider Connectedness,20 perceived harmfulness of alcohol and drug use), and explore c-ASBI's mechanism of action.

Interventions

BEHAVIORALc-ASBI

Participants in the c-ASBI group will complete a computerized screen for alcohol, cannabis, tobacco and other drugs, then view their screen score and 10 pages of information about the health effects of substance use and true-life stories on the computer. Their provider will see a report of their screen results and provide advice to stop or decrease their use, or, for those at high risk, referral to complete a computerized motivational enhancement therapy intervention.

Sponsors

Boston Children's Hospital
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
PREVENTION
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
9 Years to 20 Years
Healthy volunteers
No

Inclusion criteria

* Arriving for well or non-emergent care at one of participating study sites * Have an email address * Have internet address

Exclusion criteria

* Unable to read or understand English * Living away at college at the time of the recruitment visit * Not available for computer/telephone follow-ups * Judged by the provider to be medically or emotionally unstable at time of visit

Design outcomes

Primary

MeasureTime frameDescription
Days of alcohol use12 monthsWe will compare rates of any alcohol use over the past twelve months between the groups.

Secondary

MeasureTime frameDescription
Drinking initiation12 monthsWe will compare rates of drinking initiation over the past 12-months between groups.
Drinking cessation12 monthsWe will compare rates of drinking cessation over the past 12 months between groups.
Driving/Riding risk12 monthsWe will compare the rates of driving under the influence or riding with a driver under the influence between groups.

Other

MeasureTime frameDescription
Cannabis use12 monthsWe will compare the rates of cannabis use over the past twelve months between groups.
Tobacco use12 monthsWe will compare the rates of tobacco use over the past twelve months between groups.

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026