Actively Recruiting
Predictors of Post-COVID-19 Clinical and Cognitive Consequences
Led by VA Office of Research and Development · Updated on 2026-01-23
200
Participants Needed
1
Research Sites
206 weeks
Total Duration
On this page
Sponsors
V
VA Office of Research and Development
Lead Sponsor
J
John D. Dingell VA Medical Center
Collaborating Sponsor
AI-Summary
What this Trial Is About
The CDC describes Post-acute sequelae of SARS-COV-2 infection (PASC) for the wide range of physical and mental health consequences experienced by some patients. These sequelae may be present four or more weeks after SARS-COV-2 infection, including patients who had initial mild or asymptomatic acute infection. However, there is complete absence of data whether chronic sleep changes due to COVID-19 infection may influence these physical and mental health consequences. While fatigue is one of the common post-COVID conditions, there are no systematic examinations of sleep disturbances in COVID-19 survivors. This will be a pilot observational retrospective and prospective cohort study, to systematically assess if sleep disturbances and severity of sleep apnea comprise a modifiable facet of PASC as well as the short-term and longer-term effects of COVID-19 infection itself on sleep, cognitive function, exercise capacity and lung function.
CONDITIONS
Official Title
Predictors of Post-COVID-19 Clinical and Cognitive Consequences
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Individuals 18 years or older with a prior diagnosis of COVID-19 infection
- Both genders of all racial and ethnic groups
- Patients with obstructive sleep apnea (apnea hypopnea index of 5/hour on polysomnography) with or without prior COVID-19 infection for Aim 2
You will not qualify if you...
- Inability to give consent
- Active suicidal symptoms
- Children of all ages
- Pregnant women
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 1 location
1
John D. Dingell VA Medical Center, Detroit, MI
Detroit, Michigan, United States, 48201-1916
Actively Recruiting
Research Team
R
Ruchi Rastogi, MS
CONTACT
How is the study designed?
Study Type
OBSERVATIONAL
Masking
N/A
Allocation
N/A
Model
N/A
Primary Purpose
N/A
Number of Arms
2
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