Concussion Treatment in Older Adults Study

This study is looking into new ways to treat concussions in adults aged 50 and older. It's the first study of its kind for this age group. You might receive either standard concussion care, which includes advice on activity, hydration, nutrition, sleep, and stress management, or a "Targeted Intervention." This intervention is personalized and might include cognitive behavioral therapy (CBT) for anxiety or mood, exercises, and relaxation techniques. Researchers will measure how your concussion symptoms change using the Concussion Clinical Profiles Screening (CP Screen) at the beginning and about 30 days later. The study aims to enroll 50 participants, but its current recruitment status is unclear.

Study design
This is an interventional study with a planned enrollment of 50 participants. It uses a two-group design where participants are randomly assigned to either the intervention or usual care/control group.
What's involved
You would have an initial visit and a follow-up visit about 21-31 days later. These visits involve cognitive screening, concussion and mood questionnaires, and neuro-motor screening.
Compensation
Not stated in the trial record.
Follow-up
Your progress will be measured at study completion, which is an average of 30 days after your first visit.

AI-generated from the public study record. Only the study team can confirm whether you're eligible — confirm details with them before making decisions.

NCT05849064

Concussion Treatment in Older Adults

Completed
NAAges 50–99InterventionalTreatment
University of Pittsburgh
~56 participants
Updated 2026-08-06 on ClinicalTrials.gov
What's tested:Behavioral ControlTargeted Intervention

At a glance

Recruiting sites
0 of 1 listed site is recruiting right now
RecruitingSuspended, closed, or not yet open
What they're measuring
Concussion Clinical Profiles Screening (CP Screen)
Measured over Visit 1 (Baseline)
+1 more outcome measured
Concussion, Mild
1 sites across 1 states
Pennsylvania1
  • Anthony Kontos, PhD · PRINCIPAL_INVESTIGATOR · University of Pittsburgh

This trial hasn't published a contact. View it on ClinicalTrials.gov

Do you actually qualify for this trial?

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Eligibility criteria

Inclusion

50 years of age or older
Diagnosed concussion within the last 4 days - 12 months
Must be recruited at their initial concussion appointment
Ability to read/write to complete study assessments/testing

Exclusion

Diagnosed major psychiatric disorders other than depression/anxiety (e.g., schizophrenia)
Diagnosed with moderate to severe brain injury or past brain surgery/malformations
  • Concussion Clinical Profiles Screening (CP Screen)Visit 1 (Baseline)

    The CP Screen is a 29 item self-report, clinical profiles based symptom inventory that measures five concussion clinical profiles: 1) anxiety/mood, 2)cognitive/fatigue, 3) migraine, 4) ocular, 5) vestibular; and two modifying factors sleep and cervical. Participants indicate on a scale of 0 (none) to 3 (severe) the level of symptom severity for each item. The CP screen yields an average factor and modifier scores, with higher scores indicative of worse symptom severity, score range is 0-87.

  • Concussion Clinical Profiles Screening (CP Screen)At study completion, an average of 30 days after Visit 1

    The CP Screen is a 29 item self-report, clinical profiles based symptom inventory that measures five concussion clinical profiles: 1) anxiety/mood, 2)cognitive/fatigue, 3) migraine, 4) ocular, 5) vestibular; and two modifying factors sleep and cervical. Participants indicate on a scale of 0 (none) to 3 (severe) the level of symptom severity for each item. The CP screen yields an average factor and modifier scores, with higher scores indicative of worse symptom severity, score range is 0-87.