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Clinical Trials/NCT00249626
NCT00249626
Completed
Not Applicable

Therapists to Administer Contingency Management-Therapist Phase

UConn Health1 site in 1 country42 target enrollmentJanuary 2004
ConditionsSubstance Abuse

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Substance Abuse
Sponsor
UConn Health
Enrollment
42
Locations
1
Primary Endpoint
urinalysis results
Status
Completed
Last Updated
14 years ago

Overview

Brief Summary

The purpose of this study is to train therapists to administer contingency management (CM). This project will train up to 42 community-based treatment providers about the rationale for and the specifics of administering CM. Initial training will occur in 2-day workshops, followed by weekly supervision in delivery of CM with test cases. We expect that the majority of therapists will achieve high levels of competence and adherence in administering CM treatment within 3-5 test cases, as measured by ratings of audiotapes. To examine the efficacy of CM, each therapist who achieves adherence and competence in delivering CM will administer standard treatment alone or standard treatment plus CM to substance-abusing outpatients. In the CM condition, patients will have the opportunity to win prizes for submission of negative samples, and the treatment will be in effect for 12 weeks. In total, up to 200 patients will be randomly assigned to one of the two conditions. A research evaluator will conduct follow-up assessments, scheduled for 3, 6 and 9 months after treatment initiation.

Registry
clinicaltrials.gov
Start Date
January 2004
End Date
March 2009
Last Updated
14 years ago
Study Type
Interventional
Study Design
Single Group
Sex
All

Investigators

Sponsor
UConn Health
Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • Therapists who volunteer must have:
  • at least one-year experience treating substance abusers, and at least 6 months employment at that center
  • must commit to being available for both the workshop and individual training
  • must be willing to allow random assignment of their patients to CM and non-CM treatments

Exclusion Criteria

  • Not provided

Outcomes

Primary Outcomes

urinalysis results

Time Frame: baseline and at each follow-up

Study Sites (1)

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