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Partial Sleep Restriction in Chronic Low Back Pain: A Feasibility Study
Sponsor: University of Kansas Medical Center
Summary
Our goal is to observational study is to determine feasibility of partial sleep restriction in individuals with CLBP+I and correlation findings with features of central sensitization. * Identify feasibility of sleep restriction protocol * Identify correlation between less sleep and central sensitization Sleep will be monitored for 2 weeks (baseline sleep monitoring period). Then participants will be asked to restrict their sleep to 80% of their normal sleep duration for 5 nights (sleep restriction period). Then sleep will be monitored again for 2 weeks (sleep recovery period).
Key Details
Gender
All
Age Range
25 Years - 65 Years
Study Type
OBSERVATIONAL
Enrollment
50
Start Date
2022-07-14
Completion Date
2025-12-31
Last Updated
2025-06-06
Healthy Volunteers
Yes
Conditions
Interventions
No intervention is provided. We monitor natural recovery to full sleep.
Return to normal sleep observation.
Locations (1)
University of Kansas Medical Center
Kansas City, Kansas, United States