Tele-rehabilitation for Recreational Athletes With Patellofemoral Pain Syndrome
Usability and Effectiveness of Tele-rehabilitation Interventions on Pain, Range of Motion and Quality of Life in Recreational Athletes With Patellofemoral Pain Syndrome: A Randomized Clinical Trial
1 other identifier
interventional
26
1 country
1
Brief Summary
This study is a randomized clinical trial designed to evaluate the usability and effectiveness of a tele-rehabilitation program in recreational athletes with Patellofemoral Pain Syndrome (PFPS). A total of 26 participants aged 18-35 years with unilateral PFPS will be randomly allocated into either a conventional physiotherapy group or a tele-rehabilitation group. Both groups will receive the same evidence-based exercise protocol comprising stretching, strengthening, balance, and functional exercises over a four-week period; however, the intervention group will perform the exercises remotely using the Physitrack mobile application with regular virtual supervision and progress monitoring, while the control group will receive face-to-face physiotherapy sessions. Primary outcome measures will include pain intensity assessed by the Numerical Pain Rating Scale (NPRS), knee range of motion measured using a universal goniometer, and quality of life evaluated using the Knee Injury and Osteoarthritis Outcome Score (KOOS). The usability and patient satisfaction of the tele-rehabilitation platform will be assessed using the Telehealth Usability Questionnaire (TUQ). The findings of this study will determine whether tele-rehabilitation is a feasible, user-friendly, and effective alternative to conventional physiotherapy for improving clinical outcomes and rehabilitation accessibility in recreational athletes with PFPS.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at below P25 for not_applicable
Started Jun 2026
Shorter than P25 for not_applicable
1 active site
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
Study Start
First participant enrolled
June 9, 2026
CompletedFirst Submitted
Initial submission to the registry
July 3, 2026
CompletedFirst Posted
Study publicly available on registry
July 9, 2026
CompletedPrimary Completion
Last participant's last visit for primary outcome
August 1, 2026
CompletedStudy Completion
Last participant's last visit for all outcomes
August 1, 2026
CompletedJuly 9, 2026
June 1, 2026
2 months
July 3, 2026
July 3, 2026
Conditions
Keywords
Outcome Measures
Primary Outcomes (3)
Pain Intensity
Measured by NPRS ( Numerical Pain Rating Scale)
Base line and week 4
Range of Motion
ROM of Flexion of affected knee by Universal Goniometer
Baseline and week 4
Quality of Life in Recreational Athletes
Quality of Life is assessed through KOOS (Knee Injury and Osteoarthritis Outcome Score)
Baseline and week 4
Secondary Outcomes (1)
Telehealth Usability
week 4
Study Arms (2)
Conventional Physical Therapy Group
ACTIVE COMPARATORParticipants will receive standard face-to-face physiotherapy under the direct supervision of a licensed physiotherapist. It consists of an individualized exercise program including stretching, strengthening, functional, and balance exercises. The physiotherapist will monitor participants' performance, ensure correct exercise execution, provide feedback, and modify the treatment program according to each participant's progress throughout the period.
Tele-rehabilitation Group
EXPERIMENTALParticipants will receive a structured tele-rehabilitation program delivered through a secure digital platform under the remote supervision of a licensed physiotherapist. The intervention will consist of individualized therapeutic exercises designed to improve pain, knee function, and overall physical performance. Participants will receive exercise instructions, educational guidance, and regular remote follow-up to monitor adherence, provide feedback, and adjust the rehabilitation program based on their progress. This approach enables continuous physiotherapist support and personalized rehabilitation while allowing participants to complete their treatment remotely.
Interventions
Participants will receive supervised face-to-face physiotherapy for 4 weeks (2 sessions/week). The program will include stretching (hamstrings, quadriceps, IT band, gastrocnemius), strengthening exercises (quadriceps and hip muscles), functional exercises (mini-squats, squats, lunges), and balance training (single-leg stance and heel raises). Exercises will be progressed according to participant tolerance under the supervision of a physiotherapist.
Participants will receive a 4-week tele-rehabilitation program (2 sessions/week) delivered through the Physitrack® mobile application. The intervention will include the same standardized stretching, strengthening, functional, and balance exercises as the conventional physiotherapy group. Participants will receive individualized exercise prescriptions, instructional videos, automated reminders, and remote monitoring through the application. A physiotherapist will provide weekly telephone or video-call follow-up, monitor adherence, and progress the exercise program based on the participant's performance.
Eligibility Criteria
You may qualify if:
- Recreational athletes
- age between 18 and 35
- Males and females
- Unilateral Anterior knee pain between 3 to 6 on NPRS and retro patellar pain brought on by squatting, knee flexion, climbing, descending stairs, and extended sitting
- At least one month of knee pain
- Positive Apprehension test
- Can access the internet and smart phone
- Kujala questionnaire scale
You may not qualify if:
- Knee meniscus, ligament, and tendon injuries
- Knee effusion
- Dislocation of the patella, subluxation, and fractures
- Recent Surgery or fracture of the affected knee
- Neuromuscular, metabolic, and rheumatologic disorders.
- Who does not sign the consent form?
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
Department of Rehabilitation Sciences, The University of Faisalabad
Faisalābad, Punjan, 38000, Pakistan
Related Publications (1)
Nilmart P, Vongsirinavarat M, Khawsuwan P, Chumthong K, Tadein R, Komalasari DR. Impact of telehealth-based therapeutic exercise on pain, functional performance and dynamic knee valgus in young adult females with patellofemoral pain: a randomised controlled trial. BMJ Open Sport Exerc Med. 2024 Dec 18;10(4):e001939. doi: 10.1136/bmjsem-2024-001939. eCollection 2024.
PMID: 39720152BACKGROUND
MeSH Terms
Conditions
Interventions
Condition Hierarchy (Ancestors)
Intervention Hierarchy (Ancestors)
Study Officials
- STUDY CHAIR
Dr Muhammad Ateeb Research Associate, PhD Public Health
Research Associate , The University of Faisalabad, Faisalabad 38000, Pakistan
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
- SPONSOR
Study Record Dates
First Submitted
July 3, 2026
First Posted
July 9, 2026
Study Start
June 9, 2026
Primary Completion
August 1, 2026
Study Completion
August 1, 2026
Last Updated
July 9, 2026
Record last verified: 2026-06