ICU stay throws body clocks out of sync, new study reveals
NCT ID NCT05828680
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This study looks at how being in a hospital intensive care unit (ICU) after heart surgery affects your body's natural sleep-wake cycle. Researchers will track sleep patterns and thinking ability in 15 adults to see if disrupted rhythms slow down recovery. The goal is to understand these effects so hospitals can improve patient care.
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Study facts
What this study's own registry entry says, in plain language.
- Participants
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About 15 people
The number the study aims to enrol. It can still change while the study runs.
- Started
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Mar 2023
- Expected to finish
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Dec 2028
An estimate. End dates often move.
- Lead sponsor
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Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
Who is studied
Potential patients will be screened from outpatient clinic schedules from cardiac surgery appointments within the Perelman Center for Advanced Medicine. Patients for whom cardiac surgery is advised and who meet eligibility criteria will be approached and enrolled after their consultation with the surgeon.
- Ages
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18 years and older
- Sex
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Anyone
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: * Adults scheduled for cardiac surgery; * ≥18 years of age; * Capable of giving informed consent; * Own a smartphone (Apple devices only). Exclusion Criteria: * Taking sleep aids (antihistamines, melatonin, etc.) * History of alcohol abuse (more than 2 drinks a day with last drink within the past 3 days) * History of substance abuse at risk of postoperative withdrawal; * Active diagnosis of alcohol or substance abuse; * Recent travel across more than two (2) time zones (within the past month); * Planned travel across more than two (2) time zones during the planned study activities; * Subjects, who have received an experimental drug, used an experimental medical device within 30 days prior to screening, or who gave a blood donation of ≥ one pint within 8 weeks prior to screening; * Subjects without access to WiFi in their or close to home or at work; * Patients with hearing aids; * Heart transplant patients; * Patients in isolation.
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
Contacts and locations
Locations
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Institute for Translational Medicine and Therapeutics (ITMAT), University of Pennsylvania School of Medicine
Philadelphia, Pennsylvania, 19104, United States
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Other studies related to the condition(s) this trial covers.
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