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Clinical Trials/NCT00840151
NCT00840151
Completed
Not Applicable

A SMART Design for Attendance-based Prize CM

UConn Health1 site in 1 country360 target enrollmentJanuary 2009
ConditionsSubstance Abuse

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Substance Abuse
Sponsor
UConn Health
Enrollment
360
Locations
1
Primary Endpoint
longest duration of negative drug and alcohol samples submitted
Status
Completed
Last Updated
7 years ago

Overview

Brief Summary

The purpose of this study is to compare different forms of treatment for substance abuse. This study will involve a type of treatment called contingency management, in which patients receive incentives (prizes) for attending outpatient treatment. This study will compare contingency management to standard treatment that does not involve incentives. This study will also compare contingency management treatment that lasts 6 weeks to contingency management that lasts 12 weeks. Finally, this study will compare contingency management treatment delivered at the beginning of outpatient treatment to contingency management treatment delivered later during outpatient treatment. The investigators hypothesize that (1) a 12-week attendance-based contingency management intervention will improve retention and enhance drug abstinence versus standard treatment, (2) initial short-term exposure to attendance-based contingency management (in weeks 1-6 only) will improve substance abuse treatment outcomes compared to standard treatment alone, and (3) contingency management in weeks 7-12 will be particularly useful for those with sporadic attendance or continued drug use during initial stages of treatment.

Registry
clinicaltrials.gov
Start Date
January 2009
End Date
August 2014
Last Updated
7 years ago
Study Type
Interventional
Study Design
Factorial
Sex
All

Investigators

Sponsor
UConn Health
Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • age \> 18 years
  • current DSM-IV diagnosis of cocaine abuse or dependence or recent cocaine use (self-reported use in past 30 days or positive urine toxicology screen)
  • willing to sign informed consent and able to pass an informed consent quiz

Exclusion Criteria

  • serious, uncontrolled psychiatric illness (e.g., acute schizophrenia, bipolar disorder, severe or psychotic major depression, or suicide risk) on the basis of history or medical examination
  • in recovery from pathological gambling (meet DSM-IV criteria for lifetime pathological gambling and are actively trying to refrain from gambling)
  • do not speak English (all treatment is provided in English at these clinics)

Outcomes

Primary Outcomes

longest duration of negative drug and alcohol samples submitted

Time Frame: throughout active phase and at each follow-up assessment

Secondary Outcomes

  • proportions of samples testing negative for drugs and alcohol(during active phase and at each follow-up assessment)
  • psychosocial functioning and HIV risk behaviors(baseline, active phase and at each follow-up assessment)

Study Sites (1)

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