Actively Recruiting
Care for Veterans Post-COVID-19
Led by VA Office of Research and Development · Updated on 2025-12-24
348
Participants Needed
1
Research Sites
151 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
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. This is consistent with published expert opinion that Concordant Care underlies patients' (and clinicians') positive experiences of care for poorly understood conditions. Despite strong evidence supporting this care approach, there are no interventions to train clinicians on practices to provide Concordant Care for Veterans with poorly understood conditions such as Long-COVID. 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. This study will adapt and refine Concordant Care training for Long-COVID. 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. 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.
CONDITIONS
Official Title
Care for Veterans Post-COVID-19
Who Can Participate
Eligibility Criteria
You may qualify if you...
- English-speaking VA primary care providers are eligible for both parts of the study
- Veterans who self-identify as having Long-COVID can participate in Part 1
- Veterans meeting Long-COVID criteria by modified DePaul Symptom Questionnaire version 2 are eligible for Part 2
- Veterans must have a scheduled appointment with a participating clinician within 1 to 6 months after clinician consent for Part 2
You will not qualify if you...
- Clinicians who have already completed Concordant Care training cannot participate
- Veterans not receiving care within the VA are excluded from Part 1
- Veterans who were treated in the Intensive Care Unit (ICU) for COVID-19 are excluded from Part 2
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 1 location
1
East Orange Campus of the VA New Jersey Health Care System, East Orange, NJ
East Orange, New Jersey, United States, 07018
Actively Recruiting
Research Team
L
Lisa M McAndrew, PhD
CONTACT
S
Shannon Nugent, PhD
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
HEALTH_SERVICES_RESEARCH
Number of Arms
2
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