Alcohol Use Disorder Clinical Trial
Official title:
BioWare to Enhance Treatment for Alcohol Use Disorder and Posttraumatic Stress Disorder
NCT number | NCT05187364 |
Other study ID # | 00115253 |
Secondary ID | |
Status | Completed |
Phase | N/A |
First received | |
Last updated | |
Start date | May 5, 2022 |
Est. completion date | February 20, 2023 |
Verified date | April 2023 |
Source | Medical University of South Carolina |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
This study examines the ability of an innovative telehealth technology system to enhance Concurrent Treatment of PTSD and Substance Use Disorders using Prolonged Exposure (COPE) talk-therapy for individuals with posttraumatic stress disorder (PTSD) and alcohol use disorder.
Status | Completed |
Enrollment | 4 |
Est. completion date | February 20, 2023 |
Est. primary completion date | February 20, 2023 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 18 Years to 70 Years |
Eligibility | Inclusion Criteria: 1. Male or female; aged 18-70 years. 2. Able to provide written informed consent. 3. Meet DSM-5 diagnostic criteria for current moderate to severe alcohol use disorder. 4. Meet DSM-5 diagnostic criteria for current PTSD. 5. Participants taking psychotropic medications will be required to be maintained on a stable dose for at least 4 weeks before study initiation. Exclusion Criteria: 1. Meet DSM-5 criteria for a history of or current psychotic or bipolar disorders. 2. Current suicidal or homicidal ideation and intent. 3. Psychotropic medications which have been initiated during the past 4 weeks. 4. Acute alcohol withdrawal. 5. Pregnancy or breastfeeding for people of childbearing potential. 6. Currently enrolled in evidence based behavioral treatment for AUD or PTSD. 7. Implanted electronic devices of any kind, including pacemakers, electronic infusion pumps, stimulators, defibrillators or similar. |
Country | Name | City | State |
---|---|---|---|
United States | Medical University of South Carolina | Charleston | South Carolina |
Lead Sponsor | Collaborator |
---|---|
Medical University of South Carolina |
United States,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Percentage of participants who turn on and off equipment in 5 minutes or less | Feasibility is 80% of participants turning on and off equipment in 5 minutes or less | In-Session Visit (approximately 1 week from baseline) | |
Primary | Mean score of System Usability Scale | Acceptability is mean score of 68 or greater on System Usability Scale | Week 12 |
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