N/A
N=80
Computerized Brief Intervention vs. Delayed Computerized Brief Intervention
Drug Abuse
Bottom Line
View on ClinicalTrials.gov: NCT01936623 ↗Enrolled (actual)
80
Serious AEs
0.0%
Results posted
Jul 2017
Primary outcome: Primary: Alcohol, Smoking, and Substance Involvement Screening Tests (ASSIST) Global Continuum of Illicit Drug Risk Score — 24.4; 27.8 units on a scale
Study Design & Population
- Study type
- Interventional
- Phase
- N/A
- Interventions
- Computerized Brief Intervention (Behavioral)
- Age
- Adult, Older Adult · 18+ yrs
- Sex
- All
- Sponsor
- Friends Research Institute, Inc.
- Primary completion
- Sep 2014
Outcome Measures
| Outcome | Result | p-value |
|---|---|---|
| PRIMARY Alcohol, Smoking, and Substance Involvement Screening Tests (ASSIST) Global Continuum of Illicit Drug Risk Score |
26.4; 27.1 | — |
| SECONDARY Alcohol, Smoking, and Substance Involvement Screening Tests (ASSIST) Global Continuum of Illicit Drug Risk Score |
26.4; 27.1 | — |
Summary
The purpose of the study is to determine whether a computerized brief intervention for moderate risk drug use among adult primary care patients is more effective than providing such patients with a substance abuse assessment alone.
Eligibility Criteria
Inclusion Criteria
- (1) minimum 18 years of age
- (2) primary care or dental patients at the participating clinics
- (3) score between 4 and 26 (moderate-risk) for illicit drug and/or nonmedical use of prescription drugs on any of the single item drug use risk scores of the ASSIST.
Exclusion Criteria
- (1) score in the high-risk range on the ASSIST for any drug (except tobacco) or alcohol use (i.e., ASSIST score > 26)
- (2) no reported drug use within the past 3 months
- (3) drug abuse treatment within the past 12 months
- (4) a BI at the clinic with the behavioral health counselor within the past month
- (5) prior enrollment in the parent study;
- (6) plans to move out of New Mexico in the next 6 months
Data sourced from ClinicalTrials.gov (NCT01936623). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication.