SLEEP AND PAIN IN
SICKLE CELL DISEASE
THIS STUDY IS NO LONGER RECRUITING.
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What is this project about?
We are seeking to better understand sleep and pain in people with Sickle Cell Disease.
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These studies are approved by the Johns Hopkins Institutional Review Board (IRB00100060). The principal investigators are Claudia M. Campbell, PhD, and Jennifer A. Haythornthwaite, PhD.
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Am I eligible to participate?
We are not currently looking for participants.
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What will I be asked to do for these studies?
Your participation will involve: (1) undergoing a phone screen, (2) attending at least two in-person study visits (lasting between 2-5 hours), and (3) completing two online follow-up sessions (lasting ~1 hour each). As part of your in-person study visits, you will undergo 1-2 brain imaging sessions with sensory testing, and 5 intervention sessions to target sleep problems. We will also ask you to complete daily surveys during the study.
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Will I be compensated for my time in this study?
Yes! You can earn up to $1,025 for completing all study-related activities. We will also reimburse you for your transportation to study visits.
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How can I find out more information?
For more information, please contact Sydney Jensen at 410-550-4225, or painstudy@jhu.edu.
By artist and Sickle Cell Disease advocate, Hertz Nazaire ​