RecruitingRecruiting
Care for Veterans Post-COVID-19
NCT05787379 · VA Office of Research and Development
In plain English
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Official title
Leveraging Knowledge of Chronic Multisymptom Illness to Improve Care for Veterans
About this study
This is a two-part study. Part 1 of the study will optimize and test if a Concordant Care training improves VA clinicians' engagement in recommended practices to provide Concordant Care (i.e., validate, shared understanding, action plan) for Veterans with Long-COVID. The evidence-based Concordant Care approach involves engaging in processes that: 1) validate the patient's experience, 2) develop a shared understanding of the condition, and 3) create a patient-centered, whole health-oriented action plan to manage the condition. Concordant Care will be adapted through interviews and focus groups with Veterans with Long-COVID (estimated n=9) and primary care providers (estimated n=21). Feedback from the participants will help refine and test Concordant Care training. Part 2 of this study will determine if Concordant Care training increases clinicians' engagement in recommended practices to provide Concordant Care and will explore the effectiveness of Concordant Care on care outcomes including satisfaction, adherence to care, \& disability for Veterans with Long-COVID. Part 2 will be a randomized parallel cluster trial with primary care clinicians (n=60) separated into a Concordant Care training group and an education packet control group. Veterans (n=240) who have an upcoming appointment with their primary care provider who is a participant in the study will be recruited. The Veterans will be assessed at baseline before their appointment and approximately 3-months later after their appointment. Veterans treated by clinicians receiving Concordant Care training will report their clinician more frequently engaged in recommended conversations (i.e., ask about Long-COVID, validate experience with Long-COVID, create a shared understanding and action plan), and Veterans will perceive greater shared understanding of Long-COVID with their clinicians than Veterans treated by clinicians in the control arm.
Eligibility criteria
Inclusion Criteria:
* Part 1 and Part 2, English-speaking VA primary care providers will be included.
* Part 1, Veterans who self-identify as having Long-COVID will be included.
* Part 2, Veterans who meet criteria for Long-COVID assessed with modified DePaul Symptom Questionnaire version 2 will be included;
* Part 2, Veterans must also have a scheduled appointment with one of the participating clinicians within one to six months of the clinician being consented.
Exclusion Criteria:
* Part 1 and Part 2, clinicians who have already taken Concordant Care training will be excluded.
* Part 1, Veterans will be excluded if they are not receiving care in the VA.
* Part 2, Veterans will be excluded if they were in the Intensive Care Unit (ICU) for COVID-19.
Study design
Enrollment target: 348 participants
Allocation: randomized
Masking: none
Age groups: child, adult, older_adult
Timeline
Starts: 2025-01-01
Estimated completion: 2027-11-30
Last updated: 2025-12-24
Interventions
Behavioral: Concordant Care TrainingBehavioral: Education Packet Training
Primary outcomes
- • Concordant Care Practice Change (Baseline and 3-months)
- • Concordance of Illness Perceptions Questionnaire Change (Baseline and 3-months)
Sponsor
VA Office of Research and Development · fed
Contacts & investigators
ContactLisa M McAndrew, PhD · contact · Lisa.Mcandrew@va.gov · (862) 400-3317
ContactShannon Nugent, PhD · contact · shannon.nugent@va.gov · (503) 220-8262
InvestigatorLisa Marie McAndrew, PhD · principal_investigator, East Orange Campus of the VA New Jersey Health Care System, East Orange, NJ
All locations (1)
East Orange Campus of the VA New Jersey Health Care System, East Orange, NJRecruiting
East Orange, New Jersey, United States