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Contingency Management to Reduce Alcohol Use in a Soup Kitchen Sample (SK)

Primary Purpose

Alcohol Abuse, Contingency Management

Status
Completed
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
breath alcohol monitoring
contingency management
Sponsored by
UConn Health
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Alcohol Abuse

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

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

Sites / Locations

  • Friendship Center

Arms of the Study

Arm 1

Arm 2

Arm Type

Active Comparator

Experimental

Arm Label

breath alcohol monitoring

breath monitoring plus prize contingency management

Arm Description

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.

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.

Outcomes

Primary Outcome Measures

efficacy of contingency management relative to monitoring only
longest duration of abstinence

Secondary Outcome Measures

Full Information

First Posted
July 14, 2015
Last Updated
June 22, 2017
Sponsor
UConn Health
Collaborators
National Institute on Alcohol Abuse and Alcoholism (NIAAA)
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1. Study Identification

Unique Protocol Identification Number
NCT02499913
Brief Title
Contingency Management to Reduce Alcohol Use in a Soup Kitchen Sample
Acronym
SK
Study Type
Interventional

2. Study Status

Record Verification Date
June 2017
Overall Recruitment Status
Completed
Study Start Date
July 2015 (Actual)
Primary Completion Date
November 2016 (Actual)
Study Completion Date
November 2016 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
UConn Health
Collaborators
National Institute on Alcohol Abuse and Alcoholism (NIAAA)

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
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.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Alcohol Abuse, Contingency Management

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
27 (Actual)

8. Arms, Groups, and Interventions

Arm Title
breath alcohol monitoring
Arm Type
Active Comparator
Arm Description
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.
Arm Title
breath monitoring plus prize contingency management
Arm Type
Experimental
Arm Description
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.
Intervention Type
Behavioral
Intervention Name(s)
breath alcohol monitoring
Intervention Description
Daily breath alcohol monitoring
Intervention Type
Behavioral
Intervention Name(s)
contingency management
Intervention Description
Participants can earn chance to win prizes for negative breath alcohol samples.
Primary Outcome Measure Information:
Title
efficacy of contingency management relative to monitoring only
Description
longest duration of abstinence
Time Frame
week 4

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
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
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Carla Rash, Ph.D.
Organizational Affiliation
UConn Health
Official's Role
Principal Investigator
Facility Information:
Facility Name
Friendship Center
City
New Britain
State/Province
Connecticut
ZIP/Postal Code
06051
Country
United States

12. IPD Sharing Statement

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Contingency Management to Reduce Alcohol Use in a Soup Kitchen Sample

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