Impact of VA's Clinical Resource Hub Primary Care Telehealth Program on Health Care Use and Costs.
Kritee Gujral, Jennifer Y Scott, Clara E Dismuke-Greer...
https://pubmed.ncbi.nlm.nih.gov/40981648/Actively Recruiting
Led by VA Office of Research and Development · Updated on 2026-08-06
248
Participants Needed
1
Research Sites
13 weeks
Total Duration
Post-traumatic stress disorder PTSD and substance use disorders SUD are common and challenging mental health conditions among military Veterans, often occurring together and linked to poorer treatment outcomes. The study evaluates a new web-based training program called COPEWeb for providers, developed to improve access to Concurrent Treatment of PTSD and Substance Use Disorders Using Prolonged Exposure COPE, a trauma-focused therapy identified as a gold standard by the VA and recommended in the 2025 APA Clinical Practice Guideline for PTSD. This training aims to address the critical shortage of clinicians trained in COPE and enhance treatment delivery for Veterans with co-occurring PTSD and SUD. The study compares the new online COPEWeb training to traditional in-person COPE training for behavioral health providers, such as psychologists, psychiatrists, and counselors. COPEWeb includes an innovative provider assistance toolkit to support clinicians during therapy sessions and aims to improve training accessibility, especially for providers in rural areas. The project will develop and test COPEWeb through phases of content development, alpha-testing, and beta-testing before comparing outcomes between web-based and in-person training methods. Participants, who are providers with no prior COPE training, will attend either the online or in-person training and complete standardized patient assessments after training. Researchers will collect data on provider satisfaction, knowledge acquisition, and practice fidelity through questionnaires and knowledge tests over approximately 8 weeks. The study also measures cost-effectiveness and aims to rapidly disseminate COPEWeb to enhance evidence-based care for Veterans coping with PTSD and SUD.
CONDITIONS
COPEWeb Training for Providers
S
Sudie E Back, PhD
S
Stacey S Sellers, MS
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VA Office of Research and Development
Lead Sponsor
Medical University of South Carolina
Collaborating Sponsor
This table compares participation in this trial with other options available for this condition. The information is drawn from published research and the trial’s study details and is provided for educational purposes only.
| Factors | COPEWeb online training | COPE In‑Person training |
|---|---|---|
| What it is | Web‑based COPE training program for behavioral health providers | Traditional in‑person COPE training for behavioral health providers |
| Role in trial | Investigational arm delivering COPE training via an online platform | Active comparator arm delivering COPE training in person |
| Primary use | Training providers to deliver COPE therapy remotely | Training providers to deliver COPE therapy in traditional in‑person workshops |
| How it is given or performed | Delivered entirely online via COPEWeb platform | Delivered live in person over a 2‑day workshop (and potentially virtual), including standardized patient assessment |
| Evidence status | Effectiveness of COPEWeb is being evaluated in this trial; external evidence supports the underlying COPE therapy as first‑line for PTSD with SUD | In‑person COPE training effectiveness is established through prior COPE therapy trials and adopted as gold‑standard training |
| Important limitations | Effectiveness and usability of online training are not yet proven; relies on provider access to reliable internet | In‑person training may be less accessible or efficient, especially for providers in remote settings |
Disclaimer: This comparison is created with the help of artificial intelligence(AI) and may contain errors or missing information. It is not medical advice and does not mean one option is better or safer than another. Clinical trials are still being studied, and joining a trial is your choice. Please consult your healthcare professional before making any decisions.
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Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
1 screening visit
Duration - Approximately 8 weeks
Participants receive either the COPEWeb online training or the in-person COPE training and complete standardized patient assessments.
Training sessions and assessments during this period
Duration - Up to study completion
Researchers collect data on provider satisfaction, knowledge, and fidelity to treatment protocols to compare the effectiveness of both training methods.
Periodic questionnaires and knowledge tests
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
RANDOMIZED
Model
FACTORIAL
Primary Purpose
HEALTH_SERVICES_RESEARCH
Number of Arms
2
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Kritee Gujral, Jennifer Y Scott, Clara E Dismuke-Greer...
https://pubmed.ncbi.nlm.nih.gov/40981648/VA Office of Research and Development
Lead Sponsor
Medical University of South Carolina
Collaborating Sponsor