NCT07557784

Brief Summary

Patellofemoral pain (PFP) is a common musculoskeletal condition characterized by pain around or behind the patella during activities such as stair ambulation, squatting, running, jumping, and prolonged sitting. Exercise therapy combined with patient education is considered first-line treatment, and supervised rehabilitation is commonly used to improve adherence and clinical outcomes. Telerehabilitation may increase accessibility and reduce time and travel burden, but high-quality evidence remains limited regarding whether telerehabilitation provides outcomes that are not inferior to conventional face-to-face supervised rehabilitation in individuals with PFP. This study is a randomized, assessor-blinded, non-inferiority trial designed to compare telerehabilitation with face-to-face supervised rehabilitation in individuals with patellofemoral pain. The trial will evaluate whether telerehabilitation is not inferior to face-to-face supervised rehabilitation in improving pain and knee-related function, while also examining psychological outcomes, self-satisfaction, and adherence.

Trial Health

65
Monitor

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
106

participants targeted

Target at P50-P75 for not_applicable

Timeline
10mo left

Started May 2026

Shorter than P25 for not_applicable

Status
not yet recruiting

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

First Submitted

Initial submission to the registry

April 17, 2026

Completed
12 days until next milestone

First Posted

Study publicly available on registry

April 29, 2026

Completed
21 days until next milestone

Study Start

First participant enrolled

May 20, 2026

Expected
7 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

December 20, 2026

3 months until next milestone

Study Completion

Last participant's last visit for all outcomes

March 20, 2027

Last Updated

April 29, 2026

Status Verified

April 1, 2026

Enrollment Period

7 months

First QC Date

April 17, 2026

Last Update Submit

April 25, 2026

Conditions

Keywords

TelerehabilitationPatellofemoral Pain

Outcome Measures

Primary Outcomes (1)

  • Anterior Knee Pain Scale

    Baseline; 6 weeks; 18 weeks

Secondary Outcomes (6)

  • Numerical Rating Pain Scale

    Baseline; 6 weeks; 18 weeks

  • The Knee injury and Osteoarthritis Outcome Score

    Baseline; 6 weeks; 18 weeks

  • Tampa Scale for Kinesiophobia

    Baseline; 6 weeks; 18 weeks

  • Pain Catastrophizing Scale

    Baseline; 6 weeks; 18 weeks

  • EQ-5D-5L

    Baseline; 6 weeks; 18 weeks

  • +1 more secondary outcomes

Study Arms (2)

Telerehabilitation Group

EXPERIMENTAL

A 6-week remotely supervised rehabilitation program including education, progressive exercise therapy, and regular therapist-guided follow-up delivered through digital communication platforms.

Behavioral: Telerehabilitation

Face-to-Face Group

ACTIVE COMPARATOR

A 6-week in-person supervised rehabilitation program including education, progressive exercise therapy, and regular therapist-guided follow-up.

Behavioral: Face-to-Face Rehabilitation

Interventions

A 6-week remotely supervised rehabilitation program including education, progressive exercise therapy, and regular therapist-guided follow-up delivered through digital communication platforms.

Telerehabilitation Group

A 6-week in-person supervised rehabilitation program including education, progressive exercise therapy, and regular therapist-guided follow-up.

Face-to-Face Group

Eligibility Criteria

Age18 Years - 45 Years
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64)

You may qualify if:

  • Aged 18 to 45 years
  • Clinical diagnosis of patellofemoral pain
  • History of anterior or retropatellar knee pain for at least 3 months
  • Pain provoked by at least two of the following activities: stair ambulation, squatting, running, jumping, or prolonged sitting
  • Baseline knee pain intensity of at least 3/10 on the Numerical Rating Pain Scale
  • Willing and able to participate in the rehabilitation program and follow-up assessments
  • Able to provide written informed consent

You may not qualify if:

  • Previous knee surgery
  • History of patellar dislocation or instability
  • Evidence of ligament injury, meniscal injury requiring separate management, moderate to severe knee osteoarthritis, or other major structural knee pathology
  • Concurrent hip, ankle, lumbar spine, or other musculoskeletal disorders substantially affecting lower limb function
  • Neurological disorders affecting movement or balance
  • Severe cardiopulmonary or systemic disease contraindicating exercise
  • Received structured lower limb rehabilitation within the previous 3 months
  • Pregnancy
  • Any other condition judged by the investigators to make participation unsuitable

Contact the study team to confirm eligibility.

Sponsors & Collaborators

MeSH Terms

Conditions

Patellofemoral Pain Syndrome

Interventions

Telerehabilitation

Condition Hierarchy (Ancestors)

Joint DiseasesMusculoskeletal Diseases

Intervention Hierarchy (Ancestors)

RehabilitationAftercareContinuity of Patient CarePatient CareTherapeuticsHealth ServicesHealth Care Facilities Workforce and ServicesTelemedicineDelivery of Health CarePatient Care ManagementHealth Services Administration

Central Study Contacts

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
SINGLE
Who Masked
OUTCOMES ASSESSOR
Purpose
TREATMENT
Intervention Model
PARALLEL
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Research Fellow

Study Record Dates

First Submitted

April 17, 2026

First Posted

April 29, 2026

Study Start (Estimated)

May 20, 2026

Primary Completion (Estimated)

December 20, 2026

Study Completion (Estimated)

March 20, 2027

Last Updated

April 29, 2026

Record last verified: 2026-04

Data Sharing

IPD Sharing
Will not share