Understanding and Treating Substance Use Disorder and Comorbid Conditions in Veterans' Real-Life Settings

Status: Recruiting
Location: See location...
Intervention Type: Behavioral
Study Type: Interventional
Study Phase: Not Applicable
SUMMARY

An important part of substance use treatment for many people is learning what triggers their substance use and urges, and how they can better manage those triggers. In this study, the investigators will generate a model for each individual that shows likely causal links between their substance use, urges, and comorbid symptoms (e.g., anxiety, depression, and PTSD), and the investigators will examine these models as a group to draw conclusions about common causes for substance use (and recovery) among Veterans with substance use disorders. The investigators will also test whether receiving a personal model and clinical feedback improves substance use disorder and comorbid symptom outcomes. Results will include both patient-reported and statistically-determined causes of substance use for individuals and groups, clinical impact of a personalized model and feedback session, and participant feedback about the relevance of this study and intervention.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Healthy Volunteers: f
View:

• Inclusion criteria for this study are intended to include most Veterans with SUD

• inclusion criteria are current probable SUD as indicated by:

‣ a clinical score on the alcohol use disorders identification test (AUDIT) or drug use disorders identification test (DUDIT)

⁃ past-month substance use

⁃ a reliable access to a smartphone, tablet, or other device with capability of accessing and completing surveys throughout the day

∙ this will exclude those who are currently completing inpatient treatment

Locations
United States
Minnesota
Minneapolis VA Health Care System, Minneapolis, MN
RECRUITING
Minneapolis
Contact Information
Primary
Brittany Stevenson, PhD
Brittany.Stevenson@va.gov
(612) 467-3023
Backup
Kelvin O Lim, MD
kelvin.lim@va.gov
(612) 467-3323
Time Frame
Start Date: 2025-10-01
Estimated Completion Date: 2030-03-29
Participants
Target number of participants: 74
Treatments
Experimental: Intervention
Receive the personal causal model with a 1-hour, live clinical feedback session.
No_intervention: Control
No clinical feedback session. Personal causal models will be provided at the end of the study for those who wish to receive them.
Related Therapeutic Areas
Sponsors
Leads: VA Office of Research and Development
Collaborators: Emory University, University of Minnesota

This content was sourced from clinicaltrials.gov