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CompletedNCT02135237Updated Nov 1, 2019

Contingency Management for Alcohol Use Disorders

An interventional study of Prize Contingency Management for Alcohol Abstinence and Standard Care in Alcohol Use Disorder and Contingency Management, sponsored by UConn Health. Completed at 3 sites in United States. Open to participants aged 18 Years and older. Per ClinicalTrials.gov, last updated 2019-11-01.

Sponsored by UConn Health · Not applicable, Interventional, and Treatment

Phase
Not applicable
Study type
Interventional
Enrollment
120
Allocation
Randomized
Ages
18 Years and older
Sex
All
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Study summary

Contingency management (CM) treatments are highly efficacious in improving outcomes of substance abusing patients. However, CM has rarely been applied to individuals with alcohol use disorders, primarily because of technological limitations in monitoring drinking. The Secure Continuous Remote Alcohol Monitor (SCRAMx®) is a new technology designed to continuously monitor alcohol consumption 24 hours a day for 7 days per week. The purpose of this study is to evaluate the efficacy of CM in reducing alcohol use using SCRAMx. In total, 120 alcohol abusing or dependent patients initiating outpatient treatment at community-based clinics will be randomly assigned to one of two conditions: standard care, or standard care plus CM with reinforcement based on results of SCRAMx readings. Compared with standard care, it is expected that CM will result in fewer drinking days and longer durations of continuous non-drinking days.

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Conditions studied

  • Alcohol Use Disorder
  • Contingency Management
03

In context

Alcoholism

1,606 studies on the registry are indexed under Alcoholism; 329 are open to participants now.

This study's enrollment of 120 is above the median of 87 across 1,371 interventional studies indexed under Alcoholism.

Browse Alcoholism studies →

Lead sponsor

UConn Health is the lead sponsor of 182 studies on the registry; 18 are open to participants now.

Of its 9 completed or terminated interventional studies of FDA-regulated products, 6 (67%) have results posted.

Counted across the registry records on this site, refreshed daily.

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Who can participate

Ages eligible
18 Years and older
Sexes eligible
All
Accepts healthy volunteers
No

Inclusion criteria

  • age 18 years or older
  • current diagnosis of alcohol use disorder and self report of recent alcohol use
  • pass an informed consent quiz
  • agree to wear a SCRAMx monitor for 12 weeks
  • have a standard SCRAMx compatible phone line in their home or agree to attend the clinic weekly for brief research visits/downloads
  • agree to sign an off-campus property transfer form and return SCRAMx equipment

Exclusion criteria

Exclusion Criteria:

  • serious, uncontrolled psychiatric illness
  • in recovery from pathological gambling
  • have an unstable address
  • intend to participate in activities incompatible with SCRAMx over the next 3 months
  • are wearing SCRAMx for legal purposes
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Study design

Phase
Not applicable
Primary purpose
Treatment
Allocation
Randomized
Intervention model
Parallel assignment
Masking
None (open label)
Enrollment
120 participants (actual)

Study arms

  • Active comparator
    Control Group

    Standard Care

    Behavioral: Standard Care

  • Experimental
    Experimental Group

    Standard Care plus Prize Contingency Management for Alcohol Abstinence

    Behavioral: Prize Contingency Management for Alcohol Abstinence · Behavioral: Standard Care

Interventions

  • BehavioralPrize Contingency Management for Alcohol Abstinence

    The systematic reinforcement of desired behaviors and the withholding of reinforcement for undesired behaviors

  • BehavioralStandard Care
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What researchers measure

Primary outcomes

  1. longest duration of abstinence from alcohol

    objective report of alcohol use as measured by SCRAMx device

    Time frame: three months

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Study locations

3 sites
  • The Hospital of Central Connecticut at New Britain General
    New Britain, Connecticut 06050, United States
  • Farrell Treatment Center
    New Britain, Connecticut 06051, United States
  • Behavioral Health Network, Inc.
    Springfield, Massachusetts 01104, United States
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Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Nov 1, 2019, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
09

Registry details

Key details

Study ID
NCT02135237
Lead sponsor
UConn Health
Collaborators
National Institute on Alcohol Abuse and Alcoholism (NIAAA)
Responsible party
Sheila Alessi (Associate Professor, UConn Health) — Principal investigator
First posted
May 9, 2014
Start date
Jan 2014
Primary completion
Jun 2019
Completion
Jun 2019
Last update
Nov 1, 2019

Study contacts

Sheila Alessi, Ph.D.
principal investigator · UConn Health

Oversight

Data monitoring committee
Yes
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is completed, as verified in Oct 2019. You cannot join it, but the record below documents what was studied.

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