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Virtual Physical Therapy Support for Runners

University of Florida logo

University of Florida

Status

Enrolling

Conditions

Musculoskeletal Complication

Treatments

Behavioral: VPT

Study type

Interventional

Funder types

Other

Identifiers

NCT05994833
IRB202301005

Details and patient eligibility

About

This study will compare standard of care of home exercise for running rehabilitation to the combined treatment of home exercise with an individually provided four-session virtual physical therapy support program intervention on pain and physical function movements (controlled dual and single leg squat and lateral hopping in individuals post running injury. These collective findings will help provide new evidence of the responses to an individually provided virtual PT interventions among runners.

Enrollment

85 estimated patients

Sex

All

Ages

18 to 65 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • Age of 18 to 65 years
  • Regularly running at least 12 miles a week prior to development of musculoskeletal complaint.
  • Free of surgical history of surgery to either lower limb
  • No history of major bony injury to the lower limb such as traumatic fracture, within the past 12 months
  • Presence of chronic lower body running related injuries (e.g., patellofemoral pain, IT band syndrome, Achilles tendinitis, chronic lower back pain after running)
  • Body mass index (BMI) <=35 kg/m2

Exclusion criteria

  • Pregnant women
  • < 18 or 65 years
  • BMI >35 kg/m2
  • Mental disablement (down's syndrome or dementia)
  • Any persons incarcerated, on parole, on probation, or awaiting trial.
  • Individuals with neurologic or degenerative musculoskeletal disease, such as rheumatoid arthritis, muscular dystrophy, or Parkinson's disease.
  • Current acute running related or sport related injury (e.g., ankle sprain, hip labral tear, ACL strain during an event or run)
  • Individuals with a history of strong risk factors for poor fracture healing, such as uncontrolled diabetes, chemotherapy, end-stage organ disease, dialysis or smoking
  • Unwilling to forgo your potential in-person therapy visits for a month after enrollment

Trial design

Primary purpose

Other

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

85 participants in 2 patient groups

paper-based standard care exercise program
No Intervention group
VPT
Experimental group
Treatment:
Behavioral: VPT

Trial contacts and locations

1

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Central trial contact

Sharareh PhD, PT

Data sourced from clinicaltrials.gov

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