- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT01812187
Designing a Mobile App for Veterans With Substance Use Problems
Development of an Interactive, Adaptable and Transportable Treatment for Veterans With Substance Use Disorders
Study Overview
Status
Intervention / Treatment
Detailed Description
Many Veterans returning from Iraq and Afghanistan experience problems with drinking. There are treatments for alcohol use disorders that can be very helpful, but sometimes it can be hard for Veterans to find or participate in the treatments. This can be because of the amount of time the treatments take and the long distance to places where substance abuse treatments are offered. For Veterans who live in rural areas, these types of issues can pose even bigger problems. To address these issues, new types of treatments and ways of delivering care are being studied.
We have developed a mobile application that will be accessed through the use of a mobile device such as an ipod. The application will contain an application dedicated to the treatment of substance abuse disorders. This application will provide the coping skills and educational information to aide in helping with problems associated with drinking alcohol.
Study Type
Enrollment (Anticipated)
Phase
- Not Applicable
Contacts and Locations
Study Contact
- Name: Ken Woods
- Phone Number: 2247 713-791-14141
Study Locations
-
-
Texas
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Houston, Texas, United States, 77545
- Recruiting
- Michael E. DeBakey VA Medical Center
-
Contact:
- Ken Woods
- Phone Number: 2247 713-791-1414
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Description
Inclusion Criteria:
- Veteran of the Armed Forces
- are part of the primary care - mental health (PC-MH)
- reside in a rural community, as defined by the US Census Bureau
- score greater than or equal to 8 on the Alcohol Use Disorder Identification Test (AUDIT)
- meet diagnostic criteria for alcohol abuse or dependence as assessed by the Mini International Neuropsychiatric Inventory (MINI) according to the Diagnostic and Statistical Manual (DSM-IV)
- Age 18 and older to participate. -
Exclusion Criteria:
- Have conditions that threaten your safety (e.g., active suicidal intent, current uncontrolled psychosis or bipolar disorders in the past month as assessed by the MINI).
Veterans with a diagnosed concurrent substance dependence (other than nicotine) and more than mild risk of alcohol withdrawal based on a score of greater than 8 on the Clinical Institute Withdrawal Assessment of Alcohol (CIWA-Ar) will be excluded.
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Study Plan
How is the study designed?
Design Details
- Primary Purpose: Treatment
- Allocation: N/A
- Interventional Model: Single Group Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
---|---|
Experimental: SHIFT Cognitive Behavioral Therapy
Service to Home for Individually-Focused Therapy (SHIFT), a Cognitive Behavioral Treatment for Substance Use Disorders
|
Manualized, evidence-based, cognitive behavioral therapy for the treatment of substance abuse disorders
Other Names:
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Time Frame |
---|---|
Change
Time Frame: Change from baseline AUDIT score at 3 months
|
Change from baseline AUDIT score at 3 months
|
Collaborators and Investigators
Investigators
- Principal Investigator: Jan A Lindsay, Ph.D., Baylor College of Medicine; Michael E. Debakey VA Medical Center
Study record dates
Study Major Dates
Study Start
Primary Completion (Anticipated)
Study Completion (Anticipated)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Estimate)
Study Record Updates
Last Update Posted (Estimate)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- H-30374
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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