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IRCT20220610055129N1 IRCT 2022-06-22 University of Lahore Effects of flossing techniques along with routine exercises on pain and range of motion of knee in patients with patellofemoral pain syndrome:A randomized controlled trial effectiveness of flossing technique in addition to routine physical therapy on pain and range of motion in patients with patellofemoral pain syndrome: A randomized controlled trial 2021-12-24 anticipated 60 Complete https://irct.ir/trial/64068 interventional Randomization: Randomized, Blinding: Double blinded, Placebo: Not used, Assignment: Parallel, Purpose: Treatment, Randomization description: Total 60 participants will be randomly allocated into two groups using computer generated randomization method in which computer software will be utilized to randomly allocate participants in either group A or Group B. Then it will be concealed in and envelope and participant will be given concealed envelopes. Convenient random sampling technique will be used, Blinding description: It will be Double blinded study as assessor and caregiver will be unaware of the treatment given to patient. Treatment will be carried out in the treatment room with only patient and physiotherapist present and assessor and caregivers will not be given any information on which technique they applied to the participant. In this way they will be blinded. N/A Patellofemoral pain syndrome. Intervention 1: Control group: will receive Routine physical therapy. In routine physical therapy stabilization exercises of knee along with other exercises will be performed which includes quads sets exercises, side lying leg lift, straight leg raise, step up, wall squats. Intervention 2: Intervention group: will receive flossing exercises along with the routine physical therapy. Floss band will be used for this purpose. Yes - There is a plan to make this available What will be shared: Effects of flossing techniques along with the routine physical therapy on pain and range of motion in patients with patellofemoral pain syndrome: A randomized controlled trial All collected deidentified IPD will be shared When: Data will become available after 15 December 2022 for a period of 3 years To whom: People working in academics or who are involved in clinical trials or to students for research purposes Conditions: Data can be used for research purpose only Where to obtain: Data can be obtained by sending an email How to obtain: Data can be obtained by sending an email to dr.nusratqamar55@gmail.com Comments:
public Nusrat Qamar
Nawan pind aimnabad road, Sialkot
Sialkot Pakistan 51040 092513544112 dr.nusratqamar55@gmail.com Sialkot college of physical therapy Sialkot scientific Dr. Ashfaq Ahmad
1km.off defence road, Lahore
Lahore Pakistan 537000 09221111844844 ashfaq.ahmad@uipt.uol.edu.pk University of Lahore Pakistan Diagnosed patients with patellofemoral pain syndrome having three months history of pain Patients having positive clinical patellar test will be included 14 years 40 years Both Patients with Osteoarthritis of knee joint, patellar tendinopathy will not be included Patients with Osgood Schlatter disease Those with recent history if fracture of knee joint will not be included in the trial Those who will have had history of malignancy will not be taken into account M22.2X9 Patellofemoral disorders, unspecified knee Treatment - Other Treatment - Other Control group: will receive Routine physical therapy. In routine physical therapy stabilization exercises of knee along with other exercises will be performed which includes quads sets exercises, side lying leg lift, straight leg raise, step up, wall squats. Intervention group: will receive flossing exercises along with the routine physical therapy. Floss band will be used for this purpose. Pain. Timepoint: Primary outcome will be measured at baseline, 3rd and 6th week post intervention. Method of measurement: Pain will be assessed using Visual Analog Scale. Functional disability. Timepoint: It will be assessed at Baseline, 3rd and 6th week post intervention. Method of measurement: It will be measured using Lower Extremity Functional Index. Range of motion. Timepoint: Range of motion will be assessed at Baseline, 3rd and 6th week post intervention. Method of measurement: Range of motion will be measured using Goniometer. University of Lahore Approved 2021-12-23 Research Ethics Committee and Institutional review board of University of Lahore 1km.off defence road, Lahore Lahore Punjab Pakistan