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Clinical Trial Summary

This study is designed to assess how healthy premenopausal women respond to different patterns of sleep loss at different times in the menstrual cycle.


Clinical Trial Description

During a 1.5-week inpatient laboratory protocol, participants will undergo one of two parallel sleep conditions during either the follicular or luteal phase of the menstrual cycle (4 study arms total). Subjects will be randomly assigned to each study arm. During their time in the laboratory, biological samples (e.g., blood) will be collected for assessment of sex steroid hormones and other analyses. Sleep quantity and quality will be monitored and responses on neurobehavioral tests and surveys will be monitored for differences across conditions. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT05381532
Study type Interventional
Source Brigham and Women's Hospital
Contact Melissa A St. Hilaire, PhD
Phone 6172780620
Email msthilaire@rics.bwh.harvard.edu
Status Recruiting
Phase N/A
Start date October 17, 2022
Completion date March 31, 2026

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