Contingency Management to Reduce Alcohol Use in a Soup Kitchen Sample

NCT ID: NCT02499913

Last Updated: 2017-06-26

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Clinical Phase

NA

Total Enrollment

27 participants

Study Classification

INTERVENTIONAL

Study Start Date

2015-07-31

Study Completion Date

2016-11-30

Brief Summary

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Alcohol use and alcohol-related disorders are highly prevalent in soup kitchen users, and this population is overrepresented by minorities and disproportionately affected by alcohol-related morbidity and mortality. Contingency management is a behavioral intervention effective in reducing substance use, but few studies have evaluated the efficacy of contingency management in the context of soup kitchens or homeless programs. The investigators found that contingency management, using a twice weekly testing and reinforcement schedule, had benefits for decreasing drinking in individuals receiving services at a homeless shelter. This study will replicate and extend these earlier findings to a soup kitchen population using more sophisticated alcohol monitoring procedures to better assess the extent of drinking in this group and in response to a contingency management intervention reinforcing submission of negative breath samples. Specifically, 40 hazardous drinkers recruited from a soup kitchen will be randomly assigned to one of two conditions: alcohol monitoring or the same plus reinforcement for provision of daily negative breath alcohol samples. The interventions will be in effect for 3 weeks, and all participants will also wear transdermal continuous alcohol monitors during the intervention period. Objective and subjective indices of alcohol consumption will be evaluated and compared between and within the treatment conditions. This pilot project will provide information regarding the effect size of contingency management reinforcing negative breath samples in an important health disparities group, and results from this study will guide subsequent grant applications focusing on methods to decrease drinking in this underserved population.

Detailed Description

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Conditions

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Alcohol Abuse Contingency Management

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Primary Study Purpose

TREATMENT

Blinding Strategy

NONE

Study Groups

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breath alcohol monitoring

Breath alcohol samples and self-reports of drinking will be collected once daily at lunch and will be used as objective indicators of recent alcohol use.

Group Type ACTIVE_COMPARATOR

breath alcohol monitoring

Intervention Type BEHAVIORAL

Daily breath alcohol monitoring

breath monitoring plus prize contingency management

Breath alcohol samples and self-reports of drinking will be collected once daily at lunch and will be used as objective indicators of recent alcohol use. Participants of this group earn opportunities to draw cards from a prize bowl for negative breath samples.

Group Type EXPERIMENTAL

breath alcohol monitoring

Intervention Type BEHAVIORAL

Daily breath alcohol monitoring

contingency management

Intervention Type BEHAVIORAL

Participants can earn chance to win prizes for negative breath alcohol samples.

Interventions

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breath alcohol monitoring

Daily breath alcohol monitoring

Intervention Type BEHAVIORAL

contingency management

Participants can earn chance to win prizes for negative breath alcohol samples.

Intervention Type BEHAVIORAL

Eligibility Criteria

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Inclusion Criteria

* age ≥18
* frequent soup kitchen users who drink alcohol
* willing to wear transdermal alcohol monitor for 3 weeks
* willing to sign a property transfer form and return SCRAMx equipment

Exclusion Criteria

* uncontrolled, severe psychopathology and/or severe cognitive impairment
* non-English speaking
* in recovery for pathological gambling
* has a medical condition that would interfere with transdermal alcohol readings
* legal charges pending that are likely to lead to incarceration
Minimum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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National Institute on Alcohol Abuse and Alcoholism (NIAAA)

NIH

Sponsor Role collaborator

UConn Health

OTHER

Sponsor Role lead

Responsible Party

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Carla Rash

Professor

Responsibility Role PRINCIPAL_INVESTIGATOR

Principal Investigators

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Carla Rash, Ph.D.

Role: PRINCIPAL_INVESTIGATOR

UConn Health

Locations

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Friendship Center

New Britain, Connecticut, United States

Site Status

Countries

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United States

Other Identifiers

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P60AA003510

Identifier Type: NIH

Identifier Source: secondary_id

View Link

15-177-1

Identifier Type: -

Identifier Source: org_study_id

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