Contingency Management for Attendance - 2



Status:Completed
Conditions:Psychiatric
Therapuetic Areas:Psychiatry / Psychology
Healthy:No
Age Range:18 - Any
Updated:1/13/2017
Start Date:January 2004
End Date:January 2006

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Trial Summary
Trial Overview
Inclusion Criteria

Contingency Management for Attendance

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.


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.
We found this trial at
1
site
University of Connecticut Health Center
263 Farmington Ave
Farmington, Connecticut 06030
(860) 679-2000
University of Connecticut Health Center UConn Health is a vibrant, integrated academic medical center that...
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from
Farmington, CT
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