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Clinical Trials/NCT01784653
NCT01784653
Withdrawn
Phase 1

Randomized Controlled Trial of Computerized MET for Adolescent Substance Use

Boston Children's Hospital1 site in 1 countryOctober 2013

Overview

Phase
Phase 1
Intervention
Not specified
Conditions
Drug Abuse
Sponsor
Boston Children's Hospital
Locations
1
Primary Endpoint
Treatment engagement
Status
Withdrawn
Last Updated
9 years ago

Overview

Brief Summary

The purpose of this study is to test the effects of a computerized, self-directed Motivational Enhancement Therapy program for adolescent substance use (iMET), in comparison to clinician-delivered MET and Treatment As Usual (TAU), on treatment engagement and substance use. The investigators hypothesize that both iMET and MET will be more effective than TAU in engaging/retaining patients in treatment and in reducing substance use during a 12-month follow-up period. The investigators also hypothesize that Self-directed iMET will be as effective as the clinician-guided MET in increasing treatment engagement and abstinence during the 12-months follow-up period.

Registry
clinicaltrials.gov
Start Date
October 2013
End Date
January 2017
Last Updated
9 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Sion Kim Harris

Co-Director, Center for Adolescent Substance Abuse Research

Boston Children's Hospital

Eligibility Criteria

Inclusion Criteria

  • completed initial visit at the treatment program;
  • be available to return for iMET/MET sessions (if assigned)
  • be available to complete all follow-up measurements
  • a past-12-month CRAFFT score \>1
  • have used substances on \>6 days (not including tobacco use) during the 90 days preceding their visit

Exclusion Criteria

  • unable to speak and understand English, or read English at a 5th grade reading level
  • youth deemed by the clinical team to require immediate hospitalization or referral to more intensive residential treatment

Outcomes

Primary Outcomes

Treatment engagement

Time Frame: 12 months

We will compare the number of individual visits in the program, the number of group sessions completed, and the number of urine screens completed during a 12 month follow-up period by each participant in the three study arms.

Secondary Outcomes

  • Days abstinent(past-90-days)
  • Driving/Riding Risk(past-90-days)
  • HIV Risk Behavior(past-90-days)

Study Sites (1)

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