Lower-Cost Contingency Management in a Group Setting - 1

This study has been completed.
Sponsor:
Collaborator:
Information provided by (Responsible Party):
University of Connecticut Health Center
ClinicalTrials.gov Identifier:
NCT00249600
First received: November 3, 2005
Last updated: November 17, 2011
Last verified: November 2011
  Purpose

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.


Condition Intervention
Substance Abuse
Behavioral: Contingency management

Study Type: Interventional
Study Design: Allocation: Randomized
Endpoint Classification: Efficacy Study
Intervention Model: Single Group Assignment
Masking: Open Label
Primary Purpose: Treatment
Official Title: Lower-Cost Contingency Management in a Group Setting

Further study details as provided by University of Connecticut Health Center:

Primary Outcome Measures:
  • Drug use [ Time Frame: baseline and each follow-up ] [ Designated as safety issue: No ]

Enrollment: 172
Study Start Date: March 2003
Study Completion Date: December 2007
Primary Completion Date: December 2007 (Final data collection date for primary outcome measure)
  Eligibility

Ages Eligible for Study:   18 Years and older
Genders Eligible for Study:   Both
Accepts Healthy Volunteers:   No
Criteria

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
  Contacts and Locations
Choosing to participate in a study is an important personal decision. Talk with your doctor and family members or friends about deciding to join a study. To learn more about this study, you or your doctor may contact the study research staff using the Contacts provided below. For general information, see Learn About Clinical Studies.

Please refer to this study by its ClinicalTrials.gov identifier: NCT00249600

Locations
United States, Connecticut
University of Connecticut Health Center
Farmington, Connecticut, United States, 06030 2103
Sponsors and Collaborators
University of Connecticut Health Center
Investigators
Principal Investigator: Nancy Petry, Ph.D. University of Connecticut Health Center
  More Information

No publications provided

Responsible Party: University of Connecticut Health Center
ClinicalTrials.gov Identifier: NCT00249600     History of Changes
Other Study ID Numbers: NIDA-14618-1, R01DA014618, R01-14618-1
Study First Received: November 3, 2005
Last Updated: November 17, 2011
Health Authority: United States: Federal Government
United States: Institutional Review Board

Keywords provided by University of Connecticut Health Center:
contingency management
substance abuse

ClinicalTrials.gov processed this record on October 19, 2014