Alcohol Use Disorder Clinical Trial
— ARMS IIOfficial title:
Automated Reinforcement Management Systems, Phase II
NCT number | NCT06456905 |
Other study ID # | 19909 |
Secondary ID | |
Status | Recruiting |
Phase | N/A |
First received | |
Last updated | |
Start date | June 7, 2024 |
Est. completion date | September 1, 2025 |
The Automated Reinforcement Management Systems Phase II (ARMS II) study is a phase II trial is a randomized controlled, non-medicated assisted trial to determine the effectiveness of Contingency Management (CM) treatment for reducing alcohol drinking among adults who want to quit or reduce their alcohol consumption.
Status | Recruiting |
Enrollment | 125 |
Est. completion date | September 1, 2025 |
Est. primary completion date | September 1, 2025 |
Accepts healthy volunteers | Accepts Healthy Volunteers |
Gender | All |
Age group | 18 Years to 70 Years |
Eligibility | Inclusion Criteria: - Age 18-70 years - Have consumed 3 or more drinks in once occasion 4 or more times in the previous 30 days 3 - Have the ability to read and speak English - Have the ability to provide written informed consent - Have a breath alcohol value of 0.00 during informed consent - Owns a smartphone with an active service provider that is compatible with the study application. Exclusion Criteria: - Severe alcohol use disorder that our medical staff deems too risky for safe participation; - Significant risk of dangerous alcohol withdrawal, defined as history of seizure due to alcohol withdrawal in the last 12 months and/or expression of concern by the participant about dangerous withdrawal - Anyone aged 71 or older. - Anyone with a suicide attempt in the last 2 years. - Individuals who express concern regarding dangerous withdrawal or who exhibit dangerous withdrawal symptoms. - Individuals who do not test BrAC = 0.00 on the breathalyzer during the baseline visit. - Any other condition that investigators determine a medical or psychiatric condition that would compromise safe study participation. |
Country | Name | City | State |
---|---|---|---|
United States | Washington State University | Spokane | Washington |
Lead Sponsor | Collaborator |
---|---|
Washington State University | Managed Health Connections |
United States,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Change in days abstinent | Increase in days abstinent as verified through three consecutive negative breathalyzer samples submitted at designated time slots over a period of 12 hours. | 45 months |
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