Drug Abuse Clinical Trial
— ASPIREOfficial title:
Efficacy/Effectiveness of Unhealthy Drug Use Screening/Brief Intervention Models
Verified date | February 2012 |
Source | Boston Medical Center |
Contact | n/a |
Is FDA regulated | No |
Health authority | United States: Federal Government |
Study type | Interventional |
The objective of this study is to test whether screening and brief intervention for drug use among primary care patients leads to improved drug-related outcomes (such as decreased drug use and consequences).
Status | Completed |
Enrollment | 589 |
Est. completion date | September 2014 |
Est. primary completion date | October 2012 |
Accepts healthy volunteers | No |
Gender | Both |
Age group | 18 Years and older |
Eligibility |
Inclusion Criteria: - 18 years of age or older - Arrived for a visit in primary care - ASSIST Substance Specific Involvement Score of greater than or equal to 4 for subjects included in primary analyses; ASSIST Substance-Specific Involvement Scores of 2 or 3 for subjects included only in exploratory analyses - No previous MASBIRT intervention in the past 3 months - Fluent in English or Spanish - Two contacts who can assist with locating the subject for follow-up - Able to return to Boston Medical Center in the next 6 months for research study visits - Not pregnant (because care systems and resources differ greatly for such subjects) - Able to be interviewed by trained research staff (excluding those in acute discomfort or with significantly impaired cognition) Exclusion Criteria: - NOT 18 years of age or older - NOT Arrived for a visit in primary care - NO ASSIST Substance Specific Involvement Score of greater than or equal to 4 for subjects included in primary analyses; or NO ASSIST Substance-Specific Involvement Scores of 2 or 3 for subjects included only in exploratory analyses - ANY previous MASBIRT intervention in the past 3 months - NOT Fluent in English or Spanish - FEWER THAN two contacts who can assist with locating the subject for follow-up - NOT able to return to Boston Medical Center in the next 6 months for research study visits - Pregnant (because care systems and resources differ greatly for such subjects) - UN-Able to be interviewed by trained research staff (excluding those in acute discomfort or with significantly impaired cognition) |
Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Treatment
Country | Name | City | State |
---|---|---|---|
United States | Boston Medical Center | Boston | Massachusetts |
Lead Sponsor | Collaborator |
---|---|
Boston Medical Center | Boston University, National Institute on Drug Abuse (NIDA), RTI International |
United States,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Drug use | Six Months | No | |
Secondary | Drug use consequences | Six Months | No | |
Secondary | HIV risk behaviors | Six Months | No | |
Secondary | Substance abuse treatment utilization | Six Months | No | |
Secondary | Costs | Six Months | No |
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