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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT00840151
Other study ID # 09-053-2
Secondary ID P50DA009241-16
Status Completed
Phase N/A
First received
Last updated
Start date January 2009
Est. completion date August 2014

Study information

Verified date April 2019
Source UConn Health
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The purpose of this study is to compare different forms of treatment for substance abuse. This study will involve a type of treatment called contingency management, in which patients receive incentives (prizes) for attending outpatient treatment. This study will compare contingency management to standard treatment that does not involve incentives. This study will also compare contingency management treatment that lasts 6 weeks to contingency management that lasts 12 weeks. Finally, this study will compare contingency management treatment delivered at the beginning of outpatient treatment to contingency management treatment delivered later during outpatient treatment. The investigators hypothesize that (1) a 12-week attendance-based contingency management intervention will improve retention and enhance drug abstinence versus standard treatment, (2) initial short-term exposure to attendance-based contingency management (in weeks 1-6 only) will improve substance abuse treatment outcomes compared to standard treatment alone, and (3) contingency management in weeks 7-12 will be particularly useful for those with sporadic attendance or continued drug use during initial stages of treatment.


Recruitment information / eligibility

Status Completed
Enrollment 360
Est. completion date August 2014
Est. primary completion date August 2014
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria:

- age > 18 years

- current DSM-IV diagnosis of cocaine abuse or dependence or recent cocaine use (self-reported use in past 30 days or positive urine toxicology screen)

- willing to sign informed consent and able to pass an informed consent quiz

Exclusion Criteria:

- serious, uncontrolled psychiatric illness (e.g., acute schizophrenia, bipolar disorder, severe or psychotic major depression, or suicide risk) on the basis of history or medical examination

- in recovery from pathological gambling (meet DSM-IV criteria for lifetime pathological gambling and are actively trying to refrain from gambling)

- do not speak English (all treatment is provided in English at these clinics)

Study Design


Related Conditions & MeSH terms


Intervention

Behavioral:
contingency management
Participants randomized to a contingency management treatment condition can earn the chance to win prizes for attending substance abuse treatment.

Locations

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

Sponsors (2)

Lead Sponsor Collaborator
UConn Health National Institute on Drug Abuse (NIDA)

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary longest duration of negative drug and alcohol samples submitted throughout active phase and at each follow-up assessment
Secondary proportions of samples testing negative for drugs and alcohol during active phase and at each follow-up assessment
Secondary psychosocial functioning and HIV risk behaviors baseline, active phase and at each follow-up assessment
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