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

Sponsor
UConn Health (Other)
Overall Status
Completed
CT.gov ID
NCT02499913
Collaborator
National Institute on Alcohol Abuse and Alcoholism (NIAAA) (NIH)
27
1
2
16.1
1.7

Study Details

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.

Condition or Disease Intervention/Treatment Phase
  • Behavioral: breath alcohol monitoring
  • Behavioral: contingency management
N/A

Study Design

Study Type:
Interventional
Actual Enrollment :
27 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
None (Open Label)
Primary Purpose:
Treatment
Actual Study Start Date :
Jul 1, 2015
Actual Primary Completion Date :
Nov 1, 2016
Actual Study Completion Date :
Nov 1, 2016

Arms and Interventions

Arm Intervention/Treatment
Active Comparator: 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.

Behavioral: breath alcohol monitoring
Daily breath alcohol monitoring

Experimental: 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.

Behavioral: breath alcohol monitoring
Daily breath alcohol monitoring

Behavioral: contingency management
Participants can earn chance to win prizes for negative breath alcohol samples.

Outcome Measures

Primary Outcome Measures

  1. efficacy of contingency management relative to monitoring only [week 4]

    longest duration of abstinence

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
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

Contacts and Locations

Locations

Site City State Country Postal Code
1 Friendship Center New Britain Connecticut United States 06051

Sponsors and Collaborators

  • UConn Health
  • National Institute on Alcohol Abuse and Alcoholism (NIAAA)

Investigators

  • Principal Investigator: Carla Rash, Ph.D., UConn Health

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Carla Rash, Professor, UConn Health
ClinicalTrials.gov Identifier:
NCT02499913
Other Study ID Numbers:
  • 15-177-1
  • P60AA003510
First Posted:
Jul 16, 2015
Last Update Posted:
Jun 26, 2017
Last Verified:
Jun 1, 2017
Additional relevant MeSH terms:

Study Results

No Results Posted as of Jun 26, 2017