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NCT00249639 Clinical Trial

Contingency Management for Attendance - 2

Substance Abuse Clinical Trial

Official title:
Contingency Management for Attendance

Clinical Trial Details — Status: Completed

Administrative data
NCT number NCT00249639
Other study ID # NIDA-16855-2
Secondary ID R01-16855-2
Status Completed
Phase N/A
First received November 3, 2005
Last updated January 11, 2017
Start date January 2004
Est. completion date January 2006

Study information
Verified date May 2008
Source National Institute on Drug Abuse (NIDA)
Contact n/a
Is FDA regulated No
Health authority United States: Federal GovernmentUnited States: Institutional Review Board
Study type Interventional

Clinical Trial Summary

The purpose of this study is to evaluate the effectiveness of a low-cost contingency management procedure as compared to standard treatment. Using a cross-over design, CM is implemented at different community-based clinics and compared with non-CM in the same facilities. Research staff collects information regarding patients' demographic characteristics, attendance, and outcomes at the clinics. During Phase A (non-CM), standard clinical practice is in place. During Phase B (CM), all patients have the chance to win prizes by coming to treatment. Each participating clinic is randomly assigned to receive either the A or B phase first; each phase is in effect for 16 weeks.

Recruitment information / eligibility
Status Completed
Enrollment 300
Est. completion date January 2006
Est. primary completion date January 2006
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Subjects will be patients in treatment at one of the participating clinics during the study period. There are no other inclusion or exclusion criteria because we wish to make enrollment open to increase generalizability.

Study Design

Allocation: Non-Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Crossover Assignment, Masking: Open Label, Primary Purpose: Treatment

Related Conditions & MeSH terms

Intervention

Behavioral:
• Contingency management
Rewards valued $1-$100

Locations
Country Name City State
United States University of Connecticut Health Center Farmington Connecticut

Sponsors (2)
Lead Sponsor Collaborator
National Institute on Drug Abuse (NIDA) UConn Health

Country where clinical trial is conducted

United States, 

Outcome
Type Measure Description Time frame Safety issue
Primary Drug use baseline and each follow-up No
Primary Retention baseline and each follow-up No
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