Status:

COMPLETED

Assessing Screening Plus Brief Intervention's Resulting Efficacy (ASPIRE) to Stop Drug Use

Lead Sponsor:

Boston Medical Center

Collaborating Sponsors:

National Institute on Drug Abuse (NIDA)

Boston University

Conditions:

Drug Usage

Drug Abuse

Eligibility:

All Genders

18+ years

Phase:

PHASE3

Brief Summary

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 consequ...

Detailed Description

The efficacy of screening and brief intervention (SBI) for drug use among primary care patients is unknown. National organizations do not recommend universal screening. But policy is at odds with the ...

Eligibility Criteria

Inclusion

  • 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

  • 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)

Key Trial Info

Start Date :

April 1 2009

Trial Type :

INTERVENTIONAL

Allocation :

ACTUAL

End Date :

September 1 2014

Estimated Enrollment :

589 Patients enrolled

Trial Details

Trial ID

NCT00876941

Start Date

April 1 2009

End Date

September 1 2014

Last Update

October 2 2014

Active Locations (1)

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Page 1 of 1 (1 locations)

1

Boston Medical Center

Boston, Massachusetts, United States, 02118