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Extended Work Schedules, Sleep Loss and Health (EW and EWD)

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The University of Chicago

Status

Completed

Conditions

Sleep

Treatments

Behavioral: Fixed restricted bedtimes
Behavioral: Sleep restriction with circadian misalignment

Study type

Interventional

Funder types

Other

Identifiers

Details and patient eligibility

About

This study aims to determine whether abnormal bodily rhythms contribute to elevate the risk of diabetes, independently of the amount of sleep loss.

Enrollment

49 patients

Sex

All

Ages

21 to 39 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • normal healthy men and women between the ages of 21 years and 39 years (inclusive) with normal weight (i.e., body mass index under 28 kg/m2 in men, 27 kg/m2 in women)
  • normal findings on clinical examination, normal results on routine laboratory tests, normal EKG, normal glucose tolerance test, negative pregnancy test for women
  • no personal history of psychiatric or endocrine illness
  • no personal history of sleep disorder, usual total sleep time of at least 7 hours
  • only female volunteers with normal ovulatory cycles will be included

Exclusion criteria

  • subjects with irregular life habits (shiftworkers and subjects having traveled across time zones less than one month prior to the beginning of the baseline study)
  • subjects taking any medication (including hormonal contraceptive therapy), and smokers are excluded
  • subjects with significant sleep apnea (apnea index above 10) or significant arousal-associated periodic leg movements are excluded

Trial design

49 participants in 2 patient groups

Sleep loss and circadian alignment
Experimental group
Description:
Sleep restriction without circadian misalignment
Treatment:
Behavioral: Fixed restricted bedtimes
Sleep loss and circadian misalignment
Experimental group
Treatment:
Behavioral: Sleep restriction with circadian misalignment

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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