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RECRUITINGOBSERVATIONAL

Predictors of Post-COVID-19 Clinical and Cognitive Consequences

Predictors of Post-COVID Clinical and Cognitive Consequences

Important: This information is not medical advice. Talk to your doctor about whether a clinical trial is right for you.

About This Trial

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.

Who May Be Eligible (Plain English)

Who May Qualify: - 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 Who Should NOT Join This Trial: - Inability to give consent - Active suicidal symptoms - Children of all ages - Pregnant women Always talk to your doctor about whether this trial is right for you.

Original Eligibility Criteria

View original clinical language
Inclusion Criteria: * 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 Exclusion Criteria: * Inability to give consent * Active suicidal symptoms * Children of all ages * Pregnant women

Locations (1)

John D. Dingell VA Medical Center, Detroit, MI
Detroit, Michigan, United States