Enhanced and Attendance-based Prize CM in Community Settings

Sponsor
UConn Health (Other)
Overall Status
Completed
CT.gov ID
NCT00606853
Collaborator
National Institute on Drug Abuse (NIDA) (NIH)
443
1
4
66
6.7

Study Details

Study Description

Brief Summary

The purpose of this study is to address the conditions under which prize contingency management (CM) for abstinence and attendance may improve outcomes of cocaine-dependent patients.

For patients who initiate treatment with a cocaine-positive urine specimen, we will evaluate the efficacy of two CM procedures relative to standard, non-CM treatment. The two CM procedures will be provided as additions to standard care and will reinforce drug abstinence but will differ in expected magnitudes of prizes patients can earn, especially during early stages of abstinence. They will provide expected magnitudes of winning about $250 and $560, respectively. We expect that both CM conditions will improve retention and abstinence relative to the standard treatment, non-CM condition. If the enhanced CM condition engenders better outcomes than the $250 CM condition, this finding would suggest that patients initiating treatment while actively using cocaine may best be treated with relatively high reinforcement prize CM as an adjunct to standard care.

For patients who initiate treatment with a cocaine-negative urine specimen, we will evaluate the efficacy of a CM procedure that reinforces treatment attendance. The expected magnitude of winnings will be about $250, and again CM treatment will be in addition to standard care. This CM condition will be compared to standard treatment without CM as well as to a CM treatment that provides a similar magnitude of reinforcement, but contingent upon abstinence. Results from this study will inform an important clinical question of whether simply reinforcing attendance can improve clinical outcomes. Increased retention may result in greater exposure to therapeutic processes that may reduce drug use, especially among patients who begin treatment having already achieved some abstinence. We will also evaluate the cost-effectiveness of CM by examining the effects of the interventions on hospitalizations, medical and psychiatric care, criminal justice costs, and productivity.

Condition or Disease Intervention/Treatment Phase
  • Behavioral: Contingency Management
N/A

Study Design

Study Type:
Interventional
Actual Enrollment :
443 participants
Allocation:
Randomized
Intervention Model:
Factorial Assignment
Masking:
None (Open Label)
Primary Purpose:
Treatment
Official Title:
Enhanced and Attendance-based Prize CM in Community Settings
Study Start Date :
Oct 1, 2003
Actual Primary Completion Date :
Apr 1, 2009
Actual Study Completion Date :
Apr 1, 2009

Arms and Interventions

Arm Intervention/Treatment
Experimental: 1

Standard Treatment plus prize contingency management for abstinence with an expected probability of winning about $250 in prizes and twice-weekly breath and urine samples.

Behavioral: Contingency Management
Rewards valued $1-$100 for abstinence or treatment attendance

Experimental: 2

Standard Treatment plus prize contingency management for abstinence with an expected probability of winning about $560 in prizes and twice-weekly breath and urine samples.

Behavioral: Contingency Management
Rewards valued $1-$100 for abstinence or treatment attendance

Experimental: 3

Standard Treatment plus prize contingency management for attendance with an expected probability of winning about $250 in prizes and twice-weekly breath and urine samples.

Behavioral: Contingency Management
Rewards valued $1-$100 for abstinence or treatment attendance

No Intervention: 4

Standard Treatment

Outcome Measures

Primary Outcome Measures

  1. longest continuous period of cocaine abstinence [baseline and at each follow-up]

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • Age > 18 years

  • Current DSM-IV diagnosis of cocaine dependence

  • A cocaine-positive urine sample submitted during the first two scheduled treatment days at the center

  • Willing to provide names, addresses and phone numbers of individuals to assist in locating the patient for follow-up evaluations

  • English speaking

  • Willing to sign informed consent.

Exclusion Criteria:
  • Serious, uncontrolled psychiatric illness (e.g., acute schizophrenia, bipolar disorder, severe or psychotic major depression, or suicide risk)

  • Dementia (<23 on the Mini Mental State Exam; Folstein et al. 1975)

  • In recovery from pathological gambling

Contacts and Locations

Locations

Site City State Country Postal Code
1 UConn Health Center Farmington Connecticut United States 06030

Sponsors and Collaborators

  • UConn Health
  • National Institute on Drug Abuse (NIDA)

Investigators

  • Principal Investigator: Nancy M Petry, Ph.D., UConn Health Center

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
UConn Health
ClinicalTrials.gov Identifier:
NCT00606853
Other Study ID Numbers:
  • 04-008
  • P50DA009241
First Posted:
Feb 5, 2008
Last Update Posted:
Apr 9, 2019
Last Verified:
Apr 1, 2019
Keywords provided by UConn Health
Additional relevant MeSH terms:

Study Results

No Results Posted as of Apr 9, 2019