Contingency Management for Attendance - 2
Completed · Not applicable
Conditions studied: Substance Abuse
In brief
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.
Key facts
- Study ID
- NCT00249639
- Run by
- National Institute on Drug Abuse (NIDA)
- People needed
- 300
- Starts
- 2004-01-01
- Expected to finish
- 2006-01-01
- Last updated by the study team
- 2017-01-12
Who can join
Age: 18 and older. Sex: any. Healthy volunteers: not accepted.
Where it is running
- University of Connecticut Health Center — Farmington, Connecticut, United States
Full record on ClinicalTrials.gov
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