Actively Recruiting
Multidimensional Sleep Health Intervention to Optimize Concussion Recovery
Led by University of Colorado, Denver · Updated on 2026-05-06
54
Participants Needed
1
Research Sites
93 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
Following adolescent concussion, poor sleep health is common and relates to the development of persisting post-concussion symptoms, and uninjured adolescents (independent of concussion) also commonly experience sleep insufficiency. Given the sparse guidance that exists for clinicians to provide evidence-based sleep health recommendations for adolescents with a concussion, the primary objectives of this prospective randomized clinical trial of adolescents with a recent concussion are to discover if a multidimensional and prescriptive sleep health intervention leads to: 1) faster symptom resolution time, better sleep quality, or longer sleep duration; and 2) improved sleep habits, mental health, or academic engagement, relative to standard-of-care post-concussion sleep health guidance. Findings from this research will provide the basis for more precise sleep health recommendations for adolescents who experience a concussion.
CONDITIONS
Official Title
Multidimensional Sleep Health Intervention to Optimize Concussion Recovery
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Participants must be symptomatic at enrollment with a Post-Concussion Symptom Inventory score of 9 or higher
- Diagnosed with a concussion by a healthcare provider using American Congress of Rehabilitation Medicine criteria
- Aged 10 to 19 years (adolescents)
You will not qualify if you...
- History of treatment for sleep-related disorders before the concussion
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 1 location
1
University of Colorado Denver
Aurora, Colorado, United States, 80045
Actively Recruiting
Research Team
D
David R Howell, PhD
CONTACT
K
Katelyn Hurlburt, BS
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
DOUBLE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
TREATMENT
Number of Arms
2
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