Skip to content

AI Driven EX Versus Conventional in PFPS

Artificial Intelligence Driven Exercises Versus Conventional Exercises Therapy for Patellofemoral

Status
Not yet recruiting
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT07405034
Acronym
AI- PFPS
Enrollment
40
Registered
2026-02-12
Start date
2026-02-26
Completion date
2027-01-01
Last updated
2026-02-12

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

Conditions

Patello Femoral Pain Syndrome

Brief summary

This study aims to investigate and compare the effect of AI driven exercises program versus the conventional exercises therapy program on pain, function and dynamic knee valgus angle in treatment of patellofemoral pain syndrome.This study is randomized controlled trial and includes 40 participants .These participants divided into 2 groups (A, B), each group will be assessed with 3 measurments (vas ,dynamic knee valgus, Kujala Anterior Knee Pain Scale) and each group will receive difeerent treatments. The individuals in group A(study group) will preceive AI driven exercises program while the individual in group B will receive conventional exercises therapy program. Participants in the both groups are prescribed a 6-week comprehensive exercises program (3 sessions per week) day after day and assessment procedure will be performed pre and post treatmeant .

Detailed description

PURPOSE : This study aims to investigate and compare the effect of AI driven exercises program versus the conventional exercises therapy program on pain, function and dynamic knee valgus angle in treatment of patellofemoral pain syndrome. BACKGROUND: Patellofemoral pain syndrome (PFPS) is one of the most common knee problems that disturb function and daily activities (Menek et al .,2025). Symptoms of PFPS can develop either slowly or abruptly, and pain tends to worsen with activities such as squatting, prolonged sitting, stair climbing, jumping, or running (Menek et al .,2025). PFPS affects approximately 25% of physically active individuals (Smith et al .,2018). Core training significantly improves pain and functional limitations in patients with PFP and improves lower extremity motor performance to some extent (Y. Wang et al., 2024). These results draw more attention to the importance of the core muscle performance for both prevention and rehabilitation of the knee injuries HYPOTHESES: A-Primary Hypotheses: This study will hypothesize that: 1. There will be no significant effect of AI driven exercises program on pain in treatment of patients PFPS . 2. There will be no significant effect of AI driven exercises program on function in treatment of patients PFPS . 3. There will be no significant differences of AI driven exercises program and on dynamic knee valgus in treatment of patients PFPS. 4. There will be no significant differences of conventional exercises therapy on pain in treatment of patients PFPS. 5. There will be no significant differences of conventional exercises therapy on function in treatment of patients PFPS. 6. There will be no significant differences of conventional exercises therapy dynamic knee valgus in treatment of patients PFPS. RESEARCH QUESTION: This study will try to answer the following questions: This study will try to answer:What are the effects of of AI driven exercises program and the conventional exercises therapy program on pain, function and dynamic knee valgus angle in treatment of patellofemoral pain syndrome ?

Interventions

OTHERconventional exercises therapy program

The individual in group B will receive conventional exercises therapy program. Participants are prescribed a 6-week comprehensive exercises program (3 sessions per week) day after day and assessment procedure will be performed pre and post treatmeant

OTHERAi driven EX

The individuals in group A(study group) will preceive AI driven exercises program . Participants in the both groups are prescribed a 6-week comprehensive exercises program (3 sessions per week) day after day and assessment procedure will be performed pre and post treatmeant

Sponsors

Cairo University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Subject)

Masking description

All participants will randomized via random generator (www.randomization.com). All patients will be blinded to group allocation by ensuring that they will be unaware of the exercises performed by the other group. To maintain the blinding, the intervention sessions will be delivered separately to members of each treatment group.

Intervention model description

This study is randomized controlled trial and includes 40 participants .These participants divided into 2 groups (A, B), each group will be assessed with 3 measurments (vas ,dynamic knee valgus, Kujala Anterior Knee Pain Scale) and each group will receive difeerent treatments. The individuals in group A(study group) will preceive AI driven exercises program while the individual in group B will receive conventional exercises therapy program. Participants in the both groups are prescribed a 6-week comprehensive exercises program (3 sessions per week) day after day and assessment procedure will be performed pre and post treatmeant .

Eligibility

Sex/Gender
ALL
Age
18 Years to 40 Years
Healthy volunteers
No

Inclusion criteria

* Their ages range from 18- 40 years old, including both genders (male \& female). * Their BMI will be ≤ 29 kg/m2. * A traumatic knee pain persisting for at least three months.

Exclusion criteria

* Any congenital deformity of the lower limb, * Any recent injuries and surgeries * severe foot deformities such as hallux valgus and claw toe * Neuromuscular and neurological disorders.- history of patellofemoral dislocation, subluxation .

Design outcomes

Primary

MeasureTime frameDescription
Kujala Anterior Knee Pain Scaleup to 6 weeksa 13-item scale assessing knee functionality. The total Kujala score ranges from 0 to 100, with higher values indicating better performance. Additionally, The Kujala score is known for its reliability and validity in assessing patients with frozen PFPS

Secondary

MeasureTime frameDescription
visual analog scaleup to 6 weeksPain intensity is assessed using the visual analog scale. Participants are instructed to indicate their pain level on a line ranging from 0 to 10, with 0 representing no pain and 10 indicating unbearable pain

Countries

Egypt

Contacts

CONTACTAlaa Hamdi Rizk, master degree
alaa.potter35@gmail.com+201023429731
CONTACTDINA SAYED ABD ALLAH, Lecturer of Physical Therapy
drdinasayed_pt@yahoo.com+20 12 82742057
STUDY_DIRECTORSALWA FADL abdelmegeed, Professor of Physical Therapy

Cairo University

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 13, 2026