RECRUITING

Care for Veterans Post-COVID-19

Study Overview

This clinical trial focuses on testing the efficacy of different digital interventions to promote re-engagement in cancer-related long-term follow-up care for adolescent and young adult (AYA) survivors of childhood cancer.

Description

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.

Official Title

Leveraging Knowledge of Chronic Multisymptom Illness to Improve Care for Veterans

Quick Facts

Study Start:2025-01-01
Study Completion:2027-11-30
Study Type:Not specified
Phase:Not Applicable
Enrollment:Not specified
Status:RECRUITING

Study ID

NCT05787379

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Ages Eligible for Study:Not specified
Sexes Eligible for Study:ALL
Accepts Healthy Volunteers:No
Standard Ages:CHILD, ADULT, OLDER_ADULT
Inclusion CriteriaExclusion Criteria
  1. * Part 1 and Part 2, English-speaking VA primary care providers will be included.
  2. * Part 1, Veterans who self-identify as having Long-COVID will be included.
  3. * Part 2, Veterans who meet criteria for Long-COVID assessed with modified DePaul Symptom Questionnaire version 2 will be included;
  4. * 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.
  1. * Part 1 and Part 2, clinicians who have already taken Concordant Care training will be excluded.
  2. * Part 1, Veterans will be excluded if they are not receiving care in the VA.
  3. * Part 2, Veterans will be excluded if they were in the Intensive Care Unit (ICU) for COVID-19.

Contacts and Locations

Study Contact

Lisa M McAndrew, PhD
CONTACT
(862) 400-3317
Lisa.Mcandrew@va.gov
Shannon Nugent, PhD
CONTACT
(503) 220-8262
shannon.nugent@va.gov

Principal Investigator

Lisa Marie McAndrew, PhD
PRINCIPAL_INVESTIGATOR
East Orange Campus of the VA New Jersey Health Care System, East Orange, NJ

Study Locations (Sites)

East Orange Campus of the VA New Jersey Health Care System, East Orange, NJ
East Orange, New Jersey, 07018
United States

Collaborators and Investigators

Sponsor: VA Office of Research and Development

  • Lisa Marie McAndrew, PhD, PRINCIPAL_INVESTIGATOR, East Orange Campus of the VA New Jersey Health Care System, East Orange, NJ

Study Record Dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Registration Dates

Study Start Date2025-01-01
Study Completion Date2027-11-30

Study Record Updates

Study Start Date2025-01-01
Study Completion Date2027-11-30

Terms related to this study

Keywords Provided by Researchers

  • training
  • COVID-19
  • post-acute sequelae of COVID infection

Additional Relevant MeSH Terms

  • Post-Acute COVID-19 Syndrome