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NCT06291870 · ClinicalTrials.gov registry record

Predictors of Post-COVID-19 Clinical and Cognitive Consequences

A clinical trial of Obstructive Sleep Apnea and Post-acute Sequelae of SARS-CoV-2 Infection, sponsored by VA Office of Research and Development.

Recruiting
Registry status
200
Enrollment target
1
Study location

NCT06291870: Recruiting study of Obstructive Sleep Apnea and Post-acute Sequelae of SARS-CoV-2 Infection, sponsored by VA Office of Research and Development.

NCT06291870 is a study of Obstructive Sleep Apnea and Post-acute Sequelae of SARS-CoV-2 Infection that is actively recruiting participants, run by VA Office of Research and Development. The registered enrollment target is 200 participants, roughly in line with the 220-participant average among 155 other Obstructive Sleep Apnea trials with a reported enrollment target. The trial reports 1 study location across 1 state. According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT06291870, a study of Obstructive Sleep Apnea and Post-acute Sequelae of SARS-CoV-2 Infection, is actively recruiting participants, sponsored by VA Office of Research and Development.

RECRUITING
Registry status
200 participants
Enrollment target
1
Study location

Study Summary

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.

Primary Outcome

Trails A and Trails B test will be administered to evaluate attention and psychomotor function. This score is adjusted for age, race, gender, and years of education. Scored on a Standard scale of 100 +/- 15 for normal ranges, above 115 is above average, below 85 is considered below average.

Study Locations (1)

Michigan

  • John D. Dingell VA Medical Center, Detroit, MI - Detroit

Trial Details

FieldValue
Enrollment Target 200 participants
Start Date 2023-01-19
Est. Completion 2026-12-31
VA Office of Research and Development

1,668 total trials

What NCT06291870 shows while recruiting

NCT06291870 is an observational study that tracks outcomes without assigning an intervention. The registered 200 participants enrollment target is mid-sized for trials with a published cap, roughly in line with the 220-participant average among 155 other Obstructive Sleep Apnea trials with a reported enrollment target.

The record links to 2 conditions, with Obstructive Sleep Apnea appearing as the primary indexed condition, and to 0 interventions.

NCT06291870 reports a single indexed study location in Michigan.

Frequently Asked Questions

What is clinical trial NCT06291870 about?

NCT06291870 is a clinical study titled "Predictors of Post-COVID-19 Clinical and Cognitive Consequences". 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 ...

What is the current status of trial NCT06291870?

This trial is currently recruiting. The enrollment target is 200 participants. The study started on 2023-01-19. Estimated completion is 2026-12-31.

What conditions does trial NCT06291870 study?

This clinical trial studies the following conditions: Obstructive Sleep Apnea, Post-acute Sequelae of SARS-CoV-2 Infection.

Who is sponsoring clinical trial NCT06291870?

This trial is sponsored by VA Office of Research and Development, which has 1,668 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT06291870 being conducted?

This trial has 1 study location across Michigan. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

Similar trials for Obstructive Sleep Apnea

Matched on the same primary condition, ranked to surface studies in the same phase first, then by recruiting status, no relevance scoring or editorial curation.

Where NCT06291870's enrollment target sits among peer trials

200 39th of 155 higher than 113 of 155 other Obstructive Sleep Apnea trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Obstructive Sleep Apnea trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.

Source ClinicalTrials.gov registry export · 2026-08-08

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Source: ClinicalTrials.gov NCT06291870, the US trial registry maintained by the National Library of Medicine. NCT06291870 (mid enrollment · single site footprint · recruiting) retrieved and formatted by PlainTrial, see methodology.