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NCT06291870Recruiting

Predictors of Post-COVID-19 Clinical and Cognitive Consequences

Predictors of Post-COVID Clinical and Cognitive Consequences

Source: ClinicalTrials.gov · Last updated 23 Jan 2026

Brief summary (registry, in English)

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.

Status (registry)
Recruiting
Study type
Observational
Enrollment
200 (estimated)
First submitted
1 Mar 2024
Start date
19 Jan 2023
Primary completion date
31 Dec 2026
Lead sponsor
VA Office of Research and Development
NCT number
NCT06291870

What you commit to

  • Study type: Observational
  • Planned participants: 200
  • From 19 Jan 2023 to the primary completion date, 31 Dec 2026
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Age

  • Children of all ages

Other

  • Inability to give consent
  • Active suicidal symptoms
  • Pregnant women

Who the study is looking for

  • All individuals 18 years or older, with prior history of COVID-19 infection diagnosis
  • Both genders including all racial and ethnic groups
  • Patients with OSA (apnea hypopnea index of 5/hour on polysomnography) with history of COVID-19 infection will be eligible with prior history of COVID-19 infection and without COVID-19 for Aim 2

Age in the registry: 18 years to - · Sex: All · Accepts healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
John D. Dingell VA Medical Center, Detroit, MI
Coordinator of this site? Confirm its status
DetroitUnited StatesRecruiting

This page is information, not medical advice. Discuss any trial with your doctor.