COPEWeb Training for Providers

Sponsor
VA Office of Research and Development (U.S. Fed)
Overall Status
Not yet recruiting
CT.gov ID
NCT05812131
Collaborator
Medical University of South Carolina (Other), National Center for PTSD (U.S. Fed)
150
1
2
43.1
3.5

Study Details

Study Description

Brief Summary

PTSD and substance use disorders (SUD) are two of the most common and debilitating mental health conditions afflicting military Veterans. PTSD and SUD frequently co-occur and are associated with poorer treatment outcomes. The investigators' team developed a trauma-focused intervention, Concurrent Treatment of PTSD and Substance Use Disorders Using Prolonged Exposure (COPE), which is identified by the VA as a gold standard of behavioral healthcare. However, a critical barrier to ensuring that Veterans with co-occurring PTSD/SUD receive evidence-based treatment is a lack of provider training. This project directly addresses this critical gap by developing a new web-based training program for providers (COPEWeb).

Condition or Disease Intervention/Treatment Phase
  • Behavioral: COPEWeb online training
  • Behavioral: COPE In Person
N/A

Detailed Description

Background: PTSD is the most common mental health disorder among Veterans seeking treatment at Veterans Affairs (VA) hospitals, and more than half of Veterans with PTSD also meet criteria for a substance use disorder (SUD). To address the critical need for PTSD/SUD treatment, members of the investigative team developed Concurrent Treatment of PTSD and Substance Use Disorders Using Prolonged Exposure (COPE), an evidence-based, integrated, trauma-focused treatment identified by the VA as a gold standard of behavioral healthcare. Randomized controlled trials among Veterans demonstrate COPE's efficacy in significantly reducing PTSD and substance use. The majority of Veterans with PTSD/SUD prefer integrated treatment. Significance/Impact: At present, there is a critical shortage of clinicians trained to deliver COPE. Traditional in-person workshops are inefficient and costly. A poll of VA PTSD/SUD Specialists across the country found that 96.9% are interested in receiving COPE training and 99.1% would use a web-based training for COPE if available. A web-based resource for providers is ideal, as it can be rapidly disseminated, is easily accessible, and provides a significant amount of information in a standardized way. This project will directly address this critical gap in provider training to improve the care of Veterans with comorbid PTSD/SUD, enhance treatment delivery using innovative in-session provider assistance tools, and enhance knowledge of cost-benefit of technology-enhanced training. COPEWeb may be particularly useful for providers in rural clinic settings where mental health training is less accessible. This proposal has the potential for high military relevance and an immediate impact on dissemination and uptake of COPE, as well as a long-term impact on the overall health of the millions of Veterans suffering from co-occurring PTSD/SUD. Innovation: A new web-based provider training for COPE will be developed along with a highly innovative provider assistance toolkit to guide clinicians in real-time during sessions to enhance delivery and fidelity to the protocol and reduce provider burden. A panel of national VA experts and dissemination leaders will develop a best practice VA dissemination guideline on disseminating web-based provider trainings. The proposed project has the potential to significantly enhance provider training and increase patient access to evidence-based care. Furthermore, COPEWeb has the potential to serve a novel role in disaster planning to ensure mental health care providers are equipped to address the anticipated post-pandemic needs of Veterans given the rise in post-traumatic stress and alcohol/drug use during the pandemic. Specific Aims: This project aims to 1) develop a new web-based training protocol and innovative delivery aid system to strengthen providers' delivery of COPE to treat Veterans with PTSD/SUD with a high level of fidelity and competence, and 2) compare the COPEWeb training to in-person training on measures of knowledge, satisfaction, and behavior (i.e., fidelity). The cost effectiveness of web-based vs. in-person training will be examined. Methodology: The proposed methods and timeline for the development of COPEWeb are based on the team's prior success developing other widely-used provider training protocols (e.g.,

PEWeb, CBTIWeb). COPEWeb will be built and refined over the course of three strategic phases:

content development, alpha-testing, and beta-testing. Following beta testing, the investigators will compare COPEWeb to in-person training among clinicians. Ongoing assessment will obtain qualitative and quantitative data on measures of provider satisfaction, knowledge, and behavior. Implementation/Next Steps: In collaboration with the investigators' operations partners, VA leadership, and EBP Coordinators, COPEWeb will be rapidly disseminated to mental health providers to increase adoption of evidence-based treatment for PTSD/SUD and improve the quality of mental health care for Veterans and the nation.

Study Design

Study Type:
Interventional
Anticipated Enrollment :
150 participants
Allocation:
Randomized
Intervention Model:
Factorial Assignment
Intervention Model Description:
Providers will be randomly assigned to COPEWeb online training or in-person COPE trainingProviders will be randomly assigned to COPEWeb online training or in-person COPE training
Masking:
None (Open Label)
Primary Purpose:
Health Services Research
Official Title:
Web-Based Provider Training for Concurrent Treatment of PTSD and Substance Use Disorders Using Prolonged Exposure (COPEWeb)
Anticipated Study Start Date :
Aug 31, 2023
Anticipated Primary Completion Date :
Jan 1, 2027
Anticipated Study Completion Date :
Apr 5, 2027

Arms and Interventions

Arm Intervention/Treatment
Experimental: COPEWEb

online COPEWeb training

Behavioral: COPEWeb online training
COPE training delivered via online COPEWEb to providers

Active Comparator: COPE In person

COPE training delivered in person

Behavioral: COPE In Person
COPE training provided in person to providers

Outcome Measures

Primary Outcome Measures

  1. IBM Computer Usability Satisfaction Questionnaires (CSUQ) [Through study completion, an average of 8 weeks]

    The CSUQ is a 19-item Likert-type (7-point [strongly agree to strongly disagree]) questionnaire that provides an overall usability satisfaction score along with subscales that measure program usefulness, information quality, and interface quality. The CSUQ measure and subscales have good reliability, sensitivity, and validity.

  2. COPE Knowledge Test [Change from baseline to study completion, an average of 8 weeks]

    Pre- and post-module knowledge questions and beliefs about the effectiveness of COPE will be assessed. Two 20-item "alternate forms" versions of the knowledge measure will be created. Knowledge and beliefs will be assessed before and after completing the modules, with corrective feedback on knowledge items provided post-module.

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
Yes
Inclusion Criteria:
  • currently a provider in a behavioral health field (e.g., psychology, psychiatry) in the VA

  • at least 18 years old

  • English speaking

  • able to consistently obtain reliable internet access

  • willing to attend a 2-day "live" in-person (or virtual) COPE training if randomly assigned to that condition

  • willing to engage in a standardized patient assessment after training

  • has no prior formal training in the COPE therapy

Exclusion Criteria:
  • received prior training in COPE

  • not a provider in the behavioral health field in the VA

  • non-English speaking

  • lack of reliable internet access

  • younger than 18 years old

Contacts and Locations

Locations

Site City State Country Postal Code
1 Ralph H. Johnson VA Medical Center, Charleston, SC Charleston South Carolina United States 29401-5703

Sponsors and Collaborators

  • VA Office of Research and Development
  • Medical University of South Carolina
  • National Center for PTSD

Investigators

  • Principal Investigator: Sudie E. Back, PhD, Ralph H. Johnson VA Medical Center, Charleston, SC

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
VA Office of Research and Development
ClinicalTrials.gov Identifier:
NCT05812131
Other Study ID Numbers:
  • IIR 21-005
First Posted:
Apr 13, 2023
Last Update Posted:
Apr 13, 2023
Last Verified:
Mar 1, 2023
Individual Participant Data (IPD) Sharing Statement:
No
Plan to Share IPD:
No
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Product Manufactured in and Exported from the U.S.:
No
Keywords provided by VA Office of Research and Development
Additional relevant MeSH terms:

Study Results

No Results Posted as of Apr 13, 2023