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Exercise Program for ITB Syndrome

Efficacy of an Individualized Exercise Program for Iliotibial Band Syndrome: A Randomized Controlled Study

Status
Not yet recruiting
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06269757
Enrollment
100
Registered
2024-02-21
Start date
2025-08-01
Completion date
2026-04-01
Last updated
2025-07-30

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Iliotibial Band Syndrome

Brief summary

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.

Interventions

The individualized exercise program involves an initial 2D individual running evaluation designed for runners of all ages and abilities, to help improve performance and prevent injury. During the assessment patients receive a one-on-one evaluation with an exercise physiologist that includes: * Running analysis; * Training program review; * Strength and flexibility assessment; * Review of running video; * Personalized final report.

BEHAVIORALStandard Physical Therapy

Standard of care physical therapy for ITB band syndrome involves exercises designed to target structural weaknesses such as hip abductor weakness. Typical exercises include but are not limited to hip flexor stretches, side lying hip abduction, figure 4 bridges, lateral walks with exercise bands, and side planks.

Sponsors

NYU Langone Health
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to 65 Years
Healthy volunteers
No

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

Design outcomes

Primary

MeasureTime frameDescription
Knee injury and Osteoarthritis Outcome Score Physical Short-Form (KOOS-PS) ScoreMonth 6The KOOS-PS4 contains seven items: rising from bed, putting on socks/stockings, rising from sitting, bending to floor, twisting/pivoting on your injured knee, kneeling and squatting. Participants indicate the degree of difficulty they face in performing the items, from none to extreme. A final global score, from 0 (no problems) to 100 (extreme problems), is produced for the scale. Lower scores indicate greater physical function.
Visual Analogue Scale (VAS) ScoreMonth 6Pain is rated on a 10-point scale, from 0 (no pain) to 10 (worst possible pain). The total score is the response; lower scores indicate less pain.

Contacts

Primary ContactSamy Shelbaya
Samy.Shelbaya@nyulangone.org517-575-5522

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026