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NCT00249600 Clinical Trial

Lower-Cost Contingency Management in a Group Setting - 1

Substance Abuse Clinical Trial

Official title:
Lower-Cost Contingency Management in a Group Setting

Clinical Trial Details — Status: Completed

Administrative data
NCT number NCT00249600
Other study ID # NIDA-14618-1
Secondary ID R01DA014618R01-1
Status Completed
Phase N/A
First received November 3, 2005
Last updated November 17, 2011
Start date March 2003
Est. completion date December 2007

Study information
Verified date November 2011
Source University of Connecticut Health Center
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 efficacy of prize contingency management (CM) in enhancing attendance, reducing drug use, and improving health among clients attending two HIV drop-in centers. Specifically, 172 clients are randomly assigned to one of two 6-month treatment conditions: standard 12-step oriented group treatment, or CM group treatment. In the CM group, clients earn the chance to win prizes for submitting clean urine specimens and for complying with steps toward their treatment goals. Activities related to improving health will be emphasized, such as attending medical appointments, recording daily medication consumption, getting prescriptions filled, and attending medication adherence support groups. Group attendance, drug use, medical problems, services received, and risky drug use and sexual behaviors will be measured pre-treatment and at months 1, 3, 6, 9 and 12.

Recruitment information / eligibility
Status Completed
Enrollment 172
Est. completion date December 2007
Est. primary completion date December 2007
Accepts healthy volunteers No
Gender Both
Age group 18 Years and older
Eligibility Inclusion criteria:

- HIV-positive and a member of The Living Center or the Manchester Area Network on AIDS

- DSM-IV diagnosis of current opioid or cocaine abuse or dependence

- willingness to accept random assignment to one of the two treatment groups

Exclusion criteria:

- inability to comprehend the study (Mini-mental status score <21; Folstein & Folstein, 1975; or inability to pass an informed consent quiz)

- severely disruptive behavior

- in recovery for pathological gambling (due to potential similarity between the CM procedure and gambling)

- non-English speaking

Study Design

Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Treatment

Related Conditions & MeSH terms

Intervention

Behavioral:
• Contingency management

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

Sponsors (2)
Lead Sponsor Collaborator
University of Connecticut Health Center National Institute on Drug Abuse (NIDA)

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
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