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The Influence of Prescribed Exercise on Pain Related Fear Following Concussion in Collegiate Athletes

University of Virginia logo

University of Virginia

Status

Enrolling

Conditions

Concussion, Brain

Treatments

Behavioral: Treadmill Walking

Study type

Interventional

Funder types

Other

Identifiers

NCT06246669
HSR230522

Details and patient eligibility

About

The goal of this clinical trial is to compare the effects of acute aerobic exercise at two different intensities on psychological measures, symptomology, and time to symptom free in collegiate student athletes with concussion. The main questions it aims to answer are:

  • Does prescribed, acute aerobic exercise influence measures of pain related fear, anxiety, depression, symptoms, and recovery time?
  • Does the intensity of the exercise prescription also influence the aforementioned outcomes?

Participants will be randomly assigned into either a light intensity or moderate intensity aerobic exercise (treadmill walking) group. They will initiate the exercise protocol 48 hours following their concussion diagnosis, and complete exercise sessions 5 times per week until they report symptom-free. Researchers will compare the light intensity group to the moderate intensity group to see if intensity of exercise influences psychological measures of pain related fear, anxiety, depression, symptomology, and time to symptom-free.

Enrollment

46 estimated patients

Sex

All

Ages

18 to 25 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Collegiate athlete (varsity)
  • Symptomatic at time of exercise prescription

Exclusion criteria

  • If advanced neuroimaging was performed, any subject with a structural abnormality will be excluded
  • History of traumatic brain injury requiring hospitalization
  • Not cleared to play their sport by a physician due to some other injury such as an ankle sprain or muscle strain
  • If individual is diagnosed with any condition that is a contraindication to aerobic exercise. Please note that all participants will have already been cleared to participate in their respective collegiate sport after extensive pre-participation physical examinations upon entering the university.

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Single Blind

46 participants in 2 patient groups

Moderate Intensity
Experimental group
Description:
Treadmill walking at a rating of perceived exertion (RPE) of 13.
Treatment:
Behavioral: Treadmill Walking
Light Intensity
Experimental group
Description:
Treadmill walking at a rating of perceived exertion (RPE) of 9.
Treatment:
Behavioral: Treadmill Walking

Trial contacts and locations

1

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Central trial contact

Daniel Rosenblum, M.Ed.; Jake Resch, PhD

Data sourced from clinicaltrials.gov

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