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Search / Trial NCT06932237

Immune-mediated Pathogenic Mechanisms of Neuro-PASC in Veterans

Launched by VA OFFICE OF RESEARCH AND DEVELOPMENT · Apr 9, 2025

Trial Information

Current as of July 27, 2025

Recruiting

Keywords

Covid 19 Veterans Cognitive Post Acute Covid 19 Syndrome

ClinConnect Summary

This clinical trial is looking into the long-lasting effects of COVID-19 on mental health, specifically for Veterans who are experiencing issues like "brain fog" and other cognitive problems after their infection. The researchers want to learn more about how COVID-19 affects the brain and identify specific markers that could help in developing treatments. To do this, they will be studying Veterans who have had COVID-19 and are currently experiencing ongoing symptoms. The study will take place at two VA medical centers and aims to track cognitive function and mental health over time, while also collecting biological data to understand the connection between these symptoms and the body’s immune response.

To participate, individuals must be between the ages of 18 and 80, have tested positive for COVID-19 at least four weeks prior, and currently have symptoms related to what is known as Neuro-PASC (a term used to describe ongoing neurological issues following COVID-19). Participants will need to provide informed consent, which means they will be informed about the study and must understand what it involves. However, individuals with certain pre-existing conditions, like dementia or severe mood disorders, cannot join the study. Those who do participate can expect to engage in assessments of their cognitive and mental health over time, contributing to important research that could lead to better treatment options for those affected.

Gender

ALL

Eligibility criteria

  • Inclusion Criteria:
  • Eligible participants will:
  • have a history of SARS-CoV-2 infection 4 weeks prior to enrollment, defined as a positive PCR or home antigen test
  • be able to give informed consent as determined by brief cognitive exam and evaluation of understanding of the risks, benefits, and voluntary nature of the study
  • Additionally, participants enrolled as part of the neuro-PASC group must also:
  • currently experience neuro-PASC symptoms, not present prior to infection, as confirmed by the "Long COVID-19 Symptom Assessment" scale, a self-report measure that consists of 46 common COVID-19 sequela symptoms
  • Exclusion Criteria:
  • Exclusion criteria for all groups:
  • diagnosed with dementia, traumatic brain injury, a neurological syndrome (e.g. Parkinson disease, Alzheimer disease), or other progressive cognitive disorder before SARS-CoV-2 infection
  • diagnosed with a mood or psychotic disorder before SARS-CoV-2 infection
  • history of fibromyalgia or chronic fatigue syndrome prior to SARS-CoV-2 infection
  • unstable medical conditions or active uncontrolled autoimmune or inflammatory conditions

About Va Office Of Research And Development

The VA Office of Research and Development (ORD) is dedicated to advancing the health and well-being of veterans through innovative research initiatives. As a pivotal sponsor of clinical trials, ORD focuses on a broad spectrum of health-related topics, including mental health, rehabilitation, and chronic disease management, ensuring that findings are directly applicable to the unique needs of the veteran population. With a commitment to scientific excellence and collaboration, ORD promotes rigorous study designs and ethical standards, facilitating the translation of research discoveries into improved clinical practices and policies that enhance veteran care.

Locations

Portland, Oregon, United States

Mountain Home, Tennessee, United States

Patients applied

0 patients applied

Trial Officials

Jennifer M Loftis, MA PhD

Principal Investigator

VA Portland Health Care System, Portland, OR

Timeline

First submit

Trial launched

Trial updated

Estimated completion

Not reported