Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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NOT_YET_RECRUITING
136 participants
OBSERVATIONAL
2026-04-01
2030-12-31
Brief Summary
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Detailed Description
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Therefore, the proposed project will evaluate the effect of PASC on isolated cognitive-sensorimotor function (Aim 1), and cognitive-sensorimotor contributions to gait (Aim 2) and balance (Aim 3) dysfunction in COVID-19 survivors through an observational cross-sectional study design. Aim 1 will assess cognition, vision, proprioception, and muscle strength independent of functional task in COVID-19 survivors with and without PASC using established methods. Aim 2 will perform an instrumented assessment of gait performance of participants under a dual task scenario to stress cognition. Aim 3 will perform an instrumented assessment of postural balance under different conditions that challenge sensorimotor integration by compromising certain sensory modalities (vision, vestibular, somatosensory). A non-instrumented clinical outcome measure will also be performed as a secondary measure to evaluate a potential clinical screening tool. Based on emerging evidence, the investigators hypothesize that COVID-19 survivors with PASC will exhibit worse cognitive-sensorimotor function, dual task gait performance, and sensory-interaction balance performance than those without PASC when accounting for age, sex, and time since acute infection. PASC-induced gait and balance dysfunction has significant clinical implications as it could compromise mobility, long-term health, and quality of life of Veterans if left unaddressed.
Conditions
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Study Design
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COHORT
PROSPECTIVE
Study Groups
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Control
Adults who previously contracted Covid-19 but do not have Long-COVID.
No interventions assigned to this group
Experimental
Adults who previously contracted Covid-19 and have Long-COVID.
No interventions assigned to this group
Eligibility Criteria
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Inclusion Criteria
* Positive PCR or Rapid COVID-19 test in the past
* Onset of COVID-19 illness greater than 3 months prior to their participation in the study
* Self-reported ability to walk 10 meters with or without external assistance prior to COVID-19 illness
Exclusion Criteria
* Cognitive impairments precluding ability to provide informed consent.
* Severe acute COVID-19 infection requiring hospitalization or diagnosed post-intensive care syndrome.
* Presence of musculoskeletal, inflammatory, or neurological conditions mimicking Long COVID-19 symptoms (e.g., concussion within last 5 years, Chronic fibromyalgia, Myofascial pain syndrome, etc.)
18 Years
ALL
Yes
Sponsors
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Edward Hines Jr. VA Hospital
FED
VA Office of Research and Development
FED
Responsible Party
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Principal Investigators
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Matthew J. Major, PhD
Role: PRINCIPAL_INVESTIGATOR
Jesse Brown VA Medical Center, Chicago, IL
Keith Edward Gordon, PhD
Role: PRINCIPAL_INVESTIGATOR
Edward Hines Jr. VA Hospital, Hines, IL
Locations
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Jesse Brown VA Medical Center, Chicago, IL
Chicago, Illinois, United States
Countries
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Central Contacts
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Facility Contacts
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Other Identifiers
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RX005372
Identifier Type: OTHER_GRANT
Identifier Source: secondary_id
F5372-R
Identifier Type: -
Identifier Source: org_study_id
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