]>
IRCT20220520054932N1 IRCT 2022-05-27 The University of Faisalabad EFFECT OF MULLIGAN’S PAIN RELEASE PHENOMENON ALONG WITH KINESIOTAPING IN PATELLOFEMORAL PAIN SYNDROME EFFECT OF MULLIGAN’S PAIN RELEASE PHENOMENON ALONG WITH KINESIOTAPING IN PATELLOFEMORAL PAIN SYNDROME 2022-03-20 anticipated 40 Complete https://irct.ir/trial/63774 interventional Randomization: Randomized, Blinding: Single blinded, Placebo: Not used, Assignment: Parallel, Purpose: Treatment, Randomization description: patients that fulfill the inclusion criteria will be randomly divided into experimental and active control group by using the lottery method, Blinding description: participant is blinded means they do not know what treatment the other group gets. N/A Patellofemoral pain syndrome. Intervention 1: Intervention group: 1, this group will receive Mulligan's pain release phenomenon and baseline treatment(kinesiotaping, strengthening of vastus medialis oblique muscle and Ultrasonic) in12 sessions for 4 weeks with alternate days. compression PRP will be provided by compressing patella against condyles of femur then knee joint will be moved in flexion and extension while maintaining the compression for 15 seconds. visual analogue scale and Anterior Knee Pain scale will be used to get reading before and after the completion of treatment sessions. Intervention 2: Active Control group: Group B will be given Baseline treatment which includes Kinesiotaping of patellofemoral joint and strengthening of Vastus medialis Oblique muscle and Ultrasonic. in12 sessions for 4 weeks with alternate days.visual analogue scale and Anterior Knee Pain scale will be used to get reading before and after the completion of treatment sessions. Yes - There is a plan to make this available What will be shared: IPD collected for primary and secondary outcome measures When: Jan 2023 To whom: people working in any domain can be authorized to get this data Conditions: Any wrong information or editional errors Where to obtain: this data is only available on-demand via email mention to the person responsible How to obtain: documents can also be processed via university emails Comments: Data is private legacy respect it
public Dr Sidra Majeed
house #560, Mohalla sheikh lahory
Jhang Sadar Pakistan 35200 +92 309 1106072 hafizakinzashakoor567@yahoo.com The University of Faisalabad scientific Dr Sidra Majeed
House # 560, Mohalla sheikh lahory
Jhang Sadar Pakistan 35200 +92 309 1106072 hafizakinzashakoor567@yahoo.com The University of Faisalabad Pakistan • 18-40 years adults having PFP for more than three months • PFP bring forth during clinical examination (patellar grind test, apprehension test) • PFP in at least two functional activities (sitting for long time, stairs climbing, running, squatting, kneeling and jumping) • Both male & female • Patients with moderate pain ranging from 3 to 7 18 years 40 years Both • Any lower limb surgery in past 6 months • History of dislocation or subluxation of patella in past 6 months • Allergy from taping • Chronic illness that may limit training • Knee osteoarthritis (patellofemoral and tibiofemoral joint) • Chondromalacia patellae • Pes anserine bursitis (2) Rehabilitation Rehabilitation Intervention group: 1, this group will receive Mulligan's pain release phenomenon and baseline treatment(kinesiotaping, strengthening of vastus medialis oblique muscle and Ultrasonic) in12 sessions for 4 weeks with alternate days. compression PRP will be provided by compressing patella against condyles of femur then knee joint will be moved in flexion and extension while maintaining the compression for 15 seconds. visual analogue scale and Anterior Knee Pain scale will be used to get reading before and after the completion of treatment sessions Active Control group: Group B will be given Baseline treatment which includes Kinesiotaping of patellofemoral joint and strengthening of Vastus medialis Oblique muscle and Ultrasonic. in12 sessions for 4 weeks with alternate days.visual analogue scale and Anterior Knee Pain scale will be used to get reading before and after the completion of treatment sessions Pain. Timepoint: total 4 weeks of interventional period with alternate days contain 12 sessions. visual analogue scale will be used before and after completion of treatment session. Method of measurement: visual analogue scale. Anterior knee pain. Timepoint: total 4 weeks of interventional period with alternate days contain 12 sessions. Anterior Knee Pain scale will be used before and after completion of treatment session. Method of measurement: Anterior Knee Pain scale. The University of Faisalabad Approved 2022-03-13 Ethics committee of the university of Faisalabad house#560,Mohalla sheikh lahory Jhang Sadar Punjab Pakistan