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Immune Status After Being on Call for 24 Hrs

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The University of Chicago

Status

Enrolling

Conditions

Sleep Deprivation

Treatments

Diagnostic Test: Blood Sample Collection
Device: Actigraph (GT9X-BT) Monitor

Study type

Observational

Funder types

Other

Identifiers

NCT06636318
IRB24-1426

Details and patient eligibility

About

Sleep deprivation is a prevalent problem in modern societies. Sleep deprivation can cause hormonal changes, such as an increase in cortisol, as well as inflammation. Animal studies have shown an increase in inflammatory cytokine production following sleep deprivation. Additionally, humans experiencing sleep deprivation may experience a decrease in natural killer cells and lymphocytes.

Physicians, particularly those in surgical specialties, are often subjected to sleep deprivation as part of their medical residency training. This study hypothesizes that after 24-hour shifts, there is an increase in inflammatory response and impairment of the immune response against unspecific activation. This proposal aims to provide insight into the impact of sleep deprivation on the immune system of surgery residents by characterizing the phenotype and function of immune cells, as well as their correlation with biometric data.

Enrollment

60 estimated patients

Sex

All

Ages

18+ years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • Healthy subjects
  • Surgery residents in a 24-hour shift rotation
  • Gender of subjects: Males and females
  • Age of subjects: 18 years old and older
  • Racial and Ethnic Origin: Any race or ethnicity

Exclusion criteria

  • Unwilling/unable to sign informed consent
  • Vulnerable Subjects/Subject Capacity to provide consent

Trial design

60 participants in 1 patient group

General Surgery Residents
Description:
General Surgery residents on during 24-hour rotation shifts
Treatment:
Device: Actigraph (GT9X-BT) Monitor
Diagnostic Test: Blood Sample Collection

Trial contacts and locations

1

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Central trial contact

Angelica Perez-Gutierrez, MD; Leila Yazdanbakhsh

Data sourced from clinicaltrials.gov

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