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Clinical Trails at Rush Sleep Assessment Migraine and Non-migraine Study
Clinical Trial Protocol ID
12012506

Clinical Trial Investigator Name
Jason Ong

Clinical Trial Title

The SANDMAN Study: Sleep Assessment Across Night and Day Among Migraine and Non-Migraine Individuals



Clinical Trial Protocol Description

The purpose of this study is to investigate the sleep patterns of women with chronic migraine compared with healthy women. By conducting this study, we hope to learn more about the relationship between sleep disturbances and chronic migraine.

Participants in this study will be asked to monitor their sleep and wake patterns at home for at least 28 days. In total, the study consists of four visits to our lab, one of which includes staying in the lab for monitoring for one day and night.

Participants are compensated for their time and free parking or reimbursement for public transit is provided.



Clinical Trial Eligibility Criteria

You may be eligible to participate in this study if you:

  • Frequently experience migraines
  • Are a female between ages 18 and 41
  • Are willing to spend one day and night in the laboratory for monitoring
  • Are willing to keep track of your sleep patterns at home for at least 28 days

This is a partial list of eligibility requirements. To inquire about your eligibility, please call the contact number provided. If you wish to inquire via email, please include the title of the study in your message.





Contact Name Sarah Snyder
Contact Phone (312) 942-6575
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Sleep Assessment Migraine and Non-migraine Study

   
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