AI Driven EX Versus Conventional in PFPS

ConditionPatello Femoral Pain Syndrome

Trial statusNot yet recruiting

Trial phaseNot applicable

Trial typeInterventional

Biological sexAll

Age18-40

SponsorCairo University

About this trial

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 .

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

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.

Disqualifiers

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 .

Trial design

Design model

Parallel

Treatments tested in this trial

conventional exercises therapy program
Other intervention
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
Ai driven EX
Other intervention
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

Treatment groups

40 Participants

are divided into 2 treatment groups

Group A: ( AI driven EX for study group )Active comparator 1 intervention

Group B: conventional ex groupOther 1 intervention

Trial outcomes

Primary outcomes

Kujala Anterior Knee Pain Scale

a 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

Time frame

up to 6 weeks

Secondary outcomes

visual analog scale

Pain 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

Time frame

up to 6 weeks

Sponsors and contacts

Click on the lead sponsor to view all of their trials.

Cairo University

Lead sponsor

Source ClinicalTrials.gov

This trial is not recruiting at the moment. You can still explore other options: