Actively Recruiting

Age: 18Years +
All Genders
Healthy Volunteers
ID06636318

Impact of a 24-hour Shift Call on the Immune Status of Surgery Residents

Led by University of Chicago · Updated on 2025-12-09

60

Participants Needed

1

Research Sites

N/A

Total Duration

On this page

AI-Summary

What this Trial Is About

Sleep deprivation is a common issue that can cause hormonal changes and increase inflammation. This research focuses on surgery residents who undergo 24-hour shifts, exploring how such sleep deprivation may affect their immune system by studying immune cell types and functions along with biometric data. The study aims to better understand immune response changes during prolonged work hours. Participants include General Surgery residents working 24-hour rotation shifts. The study involves blood sample collection to examine immune cells before and after a 24-hour shift and after a month on call. Participants will also wear an Actigraph GT9X-BT device daily for a week to monitor steps, sleep, and heart rate, which will be collected at the end of the study. During the study, participants will undergo blood tests and biometric monitoring. Researchers will analyze immune cell characteristics through flow cytometry within 24 hours and compare these with biometric data such as sleep and physical activity recorded before and after rotations. The study monitors immune function and physical data over the course of a month, providing insights into how extended shifts impact immune health.

CONDITIONS

Brief Title

Immune Status After Being on Call for 24 Hrs

Who Can Participate

Age: 18Years +
All Genders
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • Healthy subjects
  • Surgery residents in a 24-hour shift rotation
  • Males and females
  • 18 years old and older
  • Any race or ethnicity
Not Eligible

You will not qualify if you...

  • Unwilling or unable to sign informed consent
  • Vulnerable subjects or unable to provide consent

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

1
2
3
+1

Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

Diagnostic Evaluation

Duration - 1 month

Participants provide blood samples to characterize the phenotype and function of immune cells before and after a 24-hour shift and after a month of being on call.

5 visits including blood sample collections and monitor returns

Long-term Monitoring

Duration - 2 weeks

Participants wear an actigraph monitor daily for one week before rotation and during the last week of rotation to collect step count, sleep, and heart rate data.

Daily use of the actigraph monitor for 14 days

Trial Site Locations

Total: 1 location

1

The University of Chicago

Chicago, Illinois, United States, 60637

Actively Recruiting

Loading map...

Research Team

A

Angelica Perez-Gutierrez, MD

L

Leila Yazdanbakhsh

How is the study designed?

Study Type

OBSERVATIONAL

Masking

N/A

Allocation

N/A

Model

N/A

Primary Purpose

N/A

Number of Arms

1

Similar Trials

Slow-wave Sleep Enhancement Using Acoustic Stimulation to Fa...

Sleep Deprivation

Actively Recruiting

1 location

Comparison of 2B-Alert Caffeine Optimization Algorithm Versu...

Sleep Deprivation

Actively Recruiting

2 locations

Cardiovascular Risk and Circadian Misalignment in Short Slee...

Sleep Deprivation

Actively Recruiting

1 location

Frequently Asked Questions

Have more questions? Get in touch with our team for quick support

Not the Right Trial for You?

Explore thousands of other clinical trials that might be a better match.
Sign up to get personalized trial recommendations delivered to your inbox.

Already have an account? Log in here