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CM Treatment for Alcohol Dependence Using New Technology

CM Treatment for Alcohol Dependence Using New Technology

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02143037
Enrollment
114
Registered
2014-05-20
Start date
2013-05-31
Completion date
2018-03-31
Last updated
2019-05-17

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Alcohol Use Disorder, Contingency Management

Brief summary

Contingency management (CM) is highly efficacious for reducing substance use, and recent data suggest that reinforcing attendance at treatment can significantly improve treatment outcomes. Importantly, CM interventions that reinforce attendance are more likely to be adopted clinically than those that reinforce abstinence. Having objective indicators of drinking outcomes, nevertheless, is critical for quantifying the benefits of attendance-based CM treatment in alcohol abusing populations. New technology is now available to gauge alcohol use in patients' natural environments. The Secure Continuous Remote Alcohol Monitor (SCRAMx®) continuously monitors alcohol consumption 24 hours a day. As such, it may be ideal for objective evaluation of alcohol consumption during treatment intervention studies, including those that involve CM. In this study, 114 patients participating in community based outpatient treatment programs for alcohol use disorders will wear SCRAMx for a 12-week period. They will be randomized to standard care or standard care plus CM, with reinforcement contingent upon attendance at treatment. The investigators will assess treatment attendance and alcohol use via SCRAMx and self reports. The investigators expect that patients randomized to the CM intervention will remain in treatment longer and show reductions in both SCRAMx assessed and self reported drinking days relative to those randomized to standard care.

Interventions

BEHAVIORALprize contingency management for attending treatment
BEHAVIORALusual care

Sponsors

National Institute on Alcohol Abuse and Alcoholism (NIAAA)
CollaboratorNIH
UConn Health
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* age 18 years or older * current diagnosis of alcohol use disorder * able to 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 at least every other week for data downloads * agree to sign an off-campus property transfer form and return SCRAMx equipment in 12 weeks

Exclusion criteria

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

Design outcomes

Primary

MeasureTime frameDescription
longest duration of actively attending treatment3 monthspatient attendance to treatment groups as verified by clinic records (number of days attended out of number of days expected to treatment)

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026