NCT07693634

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

57
Monitor

Trial Health Score

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

Trial has exceeded expected completion date
Enrollment
26

participants targeted

Target at below P25 for not_applicable

Timeline
Completed

Started Jun 2026

Shorter than P25 for not_applicable

Geographic Reach
1 country

1 active site

Status
recruiting

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

Completed
24 days until next milestone

First Submitted

Initial submission to the registry

July 3, 2026

Completed
6 days until next milestone

First Posted

Study publicly available on registry

July 9, 2026

Completed
23 days until next milestone

Primary Completion

Last participant's last visit for primary outcome

August 1, 2026

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

August 1, 2026

Completed
Last Updated

July 9, 2026

Status Verified

June 1, 2026

Enrollment Period

2 months

First QC Date

July 3, 2026

Last Update Submit

July 3, 2026

Conditions

Keywords

Anterior Knee PainTechnology assisted interventionPhysitrackfunctional performanceTelehealth Usability Questionnairepatient-centered digital therapies

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 COMPARATOR

Participants 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.

Other: Conventional Physical Therapy

Tele-rehabilitation Group

EXPERIMENTAL

Participants 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.

Other: Tele-rehabilitation

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.

Conventional Physical Therapy Group

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.

Tele-rehabilitation Group

Eligibility Criteria

Age18 Years - 35 Years
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64)

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

RECRUITING

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

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

Study Officials

  • Dr Muhammad Ateeb Research Associate, PhD Public Health

    Research Associate , The University of Faisalabad, Faisalabad 38000, Pakistan

    STUDY CHAIR

Central Study Contacts

Dr. Noreen Kiran Assit Professor

CONTACT

Dr. Muhammad Ateeb Research Associate, PhD Public Health

CONTACT

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

Locations