Telerehabilitation for Patellofemoral Pain
Telerehabilitation Versus Face-to-Face Supervised Rehabilitation for Patellofemoral Pain: A Randomized Non-Inferiority Trial
1 other identifier
interventional
106
0 countries
N/A
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
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P50-P75 for not_applicable
Started May 2026
Shorter than P25 for not_applicable
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
First Submitted
Initial submission to the registry
April 17, 2026
CompletedFirst Posted
Study publicly available on registry
April 29, 2026
CompletedStudy Start
First participant enrolled
May 20, 2026
ExpectedPrimary Completion
Last participant's last visit for primary outcome
December 20, 2026
Study Completion
Last participant's last visit for all outcomes
March 20, 2027
April 29, 2026
April 1, 2026
7 months
April 17, 2026
April 25, 2026
Conditions
Keywords
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
EXPERIMENTALA 6-week remotely supervised rehabilitation program including education, progressive exercise therapy, and regular therapist-guided follow-up delivered through digital communication platforms.
Face-to-Face Group
ACTIVE COMPARATORA 6-week in-person supervised rehabilitation program including education, progressive exercise therapy, and regular therapist-guided follow-up.
Interventions
A 6-week remotely supervised rehabilitation program including education, progressive exercise therapy, and regular therapist-guided follow-up delivered through digital communication platforms.
A 6-week in-person supervised rehabilitation program including education, progressive exercise therapy, and regular therapist-guided follow-up.
Eligibility Criteria
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
Interventions
Condition Hierarchy (Ancestors)
Intervention Hierarchy (Ancestors)
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