Leveraging Transdermal Alcohol Monitoring to Reduce Drinking Among DWI Defendants
NCT ID: NCT03638596
Last Updated: 2024-05-07
Study Results
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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COMPLETED
NA
158 participants
INTERVENTIONAL
2017-05-01
2021-03-15
Brief Summary
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Detailed Description
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Conditions
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Study Design
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RANDOMIZED
PARALLEL
TREATMENT
NONE
Study Groups
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Contingency Management
Incentive delivery contingent upon maintaining transdermal alcohol concentration below cut-off
Contingency Management
Incentive provided for changing alcohol drinking patterns based on ankle monitor
Control
Incentive delivery not contingent on transdermal alcohol concentration
Control
Incentive provided is not contingent on alcohol drinking patterns based on ankle monitor
Interventions
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Contingency Management
Incentive provided for changing alcohol drinking patterns based on ankle monitor
Control
Incentive provided is not contingent on alcohol drinking patterns based on ankle monitor
Eligibility Criteria
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Inclusion Criteria
Exclusion Criteria
* medical condition that would contraindicate participation (e.g., pregnancy, scheduled surgery)
* inability to comprehend the informed consent process or study instructions
* presence of a DSM-5 psychiatric disorder with symptoms of psychosis and/or delirium
* incarceration
21 Years
ALL
Yes
Sponsors
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National Institute on Alcohol Abuse and Alcoholism (NIAAA)
NIH
The University of Texas Health Science Center at San Antonio
OTHER
Responsible Party
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Principal Investigators
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Nathalie Hill-Kapturczak, PhD
Role: PRINCIPAL_INVESTIGATOR
The University of Texas Health Science Center San Antonio
Locations
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University of Texas Health Science Center San Antonio
San Antonio, Texas, United States
Countries
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Other Identifiers
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HSC20160425H
Identifier Type: -
Identifier Source: org_study_id
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