Actively Recruiting
Randomized Controlled Trial of Targeted Treatment in Older Adults Following Concussion
Led by University of Pittsburgh · Updated on 2026-03-05
50
Participants Needed
1
Research Sites
N/A
Total Duration
On this page
AI-Summary
What this Trial Is About
Researchers are conducting the first randomized controlled trial to study targeted treatments for concussion in adults aged 50 years or older. This research addresses the unique needs of older adults who may have sensory, cognitive, and neuro-motor challenges, making standard concussion management tools less suitable. The study aims to develop evidence for treatments tailored to this at-risk population and compare these targeted interventions to usual care. Participants will be randomly assigned to one of two groups. One group receives standardized behavioral management strategies focused on activity, hydration, nutrition, sleep, and stress management. The other group receives personalized interventions based on their specific concussion symptoms, including therapies for anxiety, mood, headache, ocular issues, cognitive challenges, sleep, and vestibular problems. These treatments are provided during two visits: the initial concussion clinical visit and a follow-up visit usually 21 to 31 days later. Throughout the study, participants complete assessments including cognitive screening, symptom questionnaires, and neuro-motor evaluations at both visits. Researchers will monitor a range of outcomes such as symptom severity, mood, dizziness, sleep quality, headache impact, cognitive function, and physical performance. Daily patient impressions of change and symptom tracking occur between visits to measure progress. The study will continue until about 30 days after the first visit, with safety and symptom monitoring throughout.
CONDITIONS
Brief Title
Concussion Treatment in Older Adults
Who Can Participate
Eligibility Criteria
You may qualify if you...
- 50 years of age or older
- Diagnosed concussion within the last 4 days to 12 months
- Must be recruited at their initial concussion appointment
- Ability to read and write to complete study assessments/testing
You will not qualify if you...
- Diagnosed major psychiatric disorders other than depression or anxiety
- Diagnosed with moderate to severe brain injury or past brain surgery/malformations
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Your Study Journey
Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
Duration - Approximately 30 days
Participants receive behavioral interventions tailored to their concussion symptoms or standardized behavioral management strategies including activity, hydration, nutrition, sleep, and stress management.
1 baseline visit and daily assessments between baseline and study completion
Trial Site Locations
Total: 1 location
1
University of Pittsburgh
Pittsburgh, Pennsylvania, United States, 15203
Actively Recruiting
Research Team
A
Anthony Kontos, PhD
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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