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OpenTrials
Completed

NCT Number: NCT02499913

Contingency Management to Reduce Alcohol Use in a Soup Kitchen Sample

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.

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Friendship Center

New Britain, Connecticut, 06051, United States

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

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

Treatment and study plan

breath alcohol monitoring

Behavioral

Daily breath alcohol monitoring

Contingency Management

Behavioral

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

Primary outcomes

  1. efficacy of contingency management relative to monitoring only

    Time frame: week 4

    longest duration of abstinence

Sponsors and collaborators

Lead sponsor

UConn Health

Other

Collaborators

  • National Institute on Alcohol Abuse and Alcoholism (NIAAA)

Registry information

Acronym: SK

Important dates

Study start
2015
Primary completion
2016
Study completion
2016
First posted
Jul 16, 2015
Registry last updated
Jun 26, 2017

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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