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Multidimensional Sleep Health Intervention to Optimize Concussion Recovery

Recruiting

Multidimensional Sleep Health Intervention to Optimize Concussion Recovery: A Randomized Clinical Trial

Who can join

Ages 10 to 19 · All sexes

Full eligibility criteria
Inclusion Criteria:

* Participants will be symptomatic at the time of enrollment (Post-Concussion Symptom Inventory \[PCSI\] score ≥9)
* Diagnosed with a concussion by a healthcare provider using the American Congress of Rehabilitation Medicine diagnostic criteria
* 10-19 years of age (aligned with World Health Organization definition of 'adolescent')

Exclusion Criteria:

* History of treatment for pre-concussion sleep-related disorders

About the study

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.

What is being tested

Sponsor: University of Colorado, Denver · Participants: 54 · Started: Sep 10, 2025

Contact the study team

Official record on ClinicalTrials.gov — NCT07082218

Locations in the U.S.

ColoradoUniversity of Colorado Denver, Aurora

Conditions

From ClinicalTrials.gov, data retrieved Sep 30, 2026. Each study sets its own eligibility; the study team decides who can join.