Skip to content

Computerized Screening and Brief Physician Advice to Reduce Teen Drinking

Computerized Screening and Brief Physician Advice to Reduce Teen Drinking

Status
Withdrawn
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT00849589
Enrollment
0
Registered
2009-02-24
Start date
2010-01-31
Completion date
2014-12-31
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, Risk Behavior

Keywords

Screening, Brief intervention, Underage drinking

Brief summary

The goal of this project is to adapt a computerized Screening and Brief Advice (SBA) protocol that has demonstrated efficacy in reducing underage drinking among adolescent primary care patients and then to test it in a multi-site randomized controlled trial (RCT).

Detailed description

The specific aims of the proposed multisite RCT are: 1. To establish the efficacy of the computerized SBA protocol on alcohol use, on DWI/RWID, and other alcohol-related health risk behaviors; 2. To test the effect of Technological Extenders (TE) on prolonging the beneficial effects of the SBA protocol; 3. To identify moderators, mediators, and optimal responders to the SBA/TE interventions; 4. To examine the association between cessation of underage drinking and other health-risk behaviors in an adolescent primary care sample.

Interventions

BEHAVIORALComputerized screening and brief physician advice

Participants complete screening for alcohol use and other health risk behaviors on the computer, receive some related health information on the computer, and meet with a primary care provider for a short discussion of health risk behaviors

BEHAVIORALComputerized SBA with technological extenders

Participants complete screening for alcohol use and other health risk behaviors on the computer, receive some related health information on the computer, and meet with a primary care provider for a short discussion of health risk behaviors. In addition, the provider sends them a brief email or text message at 4 months and 9 months after study entry to reinforce the brief advice.

Sponsors

Cambridge Health Alliance
CollaboratorOTHER
Dartmouth-Hitchcock Medical Center
CollaboratorOTHER
Fallon Clinic
CollaboratorINDUSTRY
Tufts Medical Center
CollaboratorOTHER
University of Vermont
CollaboratorOTHER
Boston Children's Hospital
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
SCREENING
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
12 Years to 21 Years
Healthy volunteers
Yes

Inclusion criteria

* 12-21 years old * patients arriving for routine medical care * provide informed assent (for those \<18) or informed consent (for those 18-21)

Exclusion criteria

* medically or psychologically unstable at time of visit * receiving behavioral health services * cannot read or understand English at a 6th grade reading level * unavailable for follow-up assessments

Design outcomes

Primary

MeasureTime frame
Initiation of underage drinkingBaseline, 3-months, 6-months, 12-months

Secondary

MeasureTime frame
Cessation of underage drinkingBaseline, 3-months, 6-months, 12-months

Countries

United States

Outcome results

None listed

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