Actively Recruiting

Phase Not Applicable
Age: 50Years - 99Years
All Genders
ID05849064

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

Age: 50Years - 99Years
All Genders

Eligibility Criteria

Eligible

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
Not Eligible

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

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

Outpatient Treatment

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

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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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