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Exercise Program for ITB Syndrome

NYU Langone Health logo

NYU Langone Health

Status

Not yet enrolling

Conditions

Iliotibial Band Syndrome

Treatments

Behavioral: Standard Physical Therapy
Behavioral: Individualized Exercise Program

Study type

Interventional

Funder types

Other

Identifiers

NCT06269757
23-01514

Details and patient eligibility

About

Patients with diagnosed iliotibial band (ITB) syndrome indicated for non-operative management will be randomized to individualized exercise program or standard physical therapy over the course of 3 months to determine any possible difference in clinical outcomes.

Enrollment

100 estimated patients

Sex

All

Ages

18 to 65 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Clinical diagnosis of ITB syndrome
  • Age 18-65
  • Ability to comply with a standardized physical therapy protocol
  • Willing and able to provide consent

Exclusion criteria

  • Patients at any increased risk of falls or at increased risk from harm due to falling, including issues with vertigo, osteoporosis, or a history of past falls
  • Patient otherwise deemed at increased risk from this investigational rehabilitation program by their referring surgeon or physical therapist
  • Patients who are pregnant

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

100 participants in 2 patient groups

Individualized Exercise Program
Experimental group
Description:
Patients with diagnosed ITB syndrome indicated for non-operative management who are assigned to an individualized exercise program. Duration of therapy will be approximately 3 months. Patients will be followed for 6 months to assess longitudinal outcomes.
Treatment:
Behavioral: Individualized Exercise Program
Standard Physical Therapy
Active Comparator group
Description:
Patients with diagnosed ITB syndrome indicated for non-operative management who are assigned to receive standard physical therapy. Duration of therapy will be approximately 3 months. Patients will be followed for 6 months to assess longitudinal outcomes.
Treatment:
Behavioral: Standard Physical Therapy

Trial contacts and locations

0

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Central trial contact

Samy Shelbaya

Data sourced from clinicaltrials.gov

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