Clinical Trials Logo

Clinical Trial Summary

Objective: to investigate whether females with PF OA descend stairs with different muscular recruitment strategies contrasted with similar aged healthy females. Methods: An observational comparative study will be conducted with thirty females with PF OA and 10 healthy ones. The onset times and electromyography (EMG) duration of multifidus, transversus abdominus (TrA), gluteus medius (GM), and vasti muscles will be measured by quantitative EMG during stair descent task. hypothesis: Investigators hypothesize that there won't be a significant difference between females with PF OA and their matched healthy group regarding the onset times and duration of vastus medialis obliqus (VMO), vastus lateralis (VL), gluteus medius (GM), multifidus, and transversus abdominus (TrA), during stair descent task.


Clinical Trial Description

Investigators will collect the EMG activity of VMO, VL, GM, multifidus, and TrA using bipolar Ag-AgCl disposable surface electrodes (Better signal solution medical supply Co., limited, Zhongshan, China) and eight channels highresolution wireless bio amplifier (WBA) system (Biomation, Almonte, Canada). Electromyographic data will be sampled at 1000 Hz and bandpass filtered at 50-200 Hz. For each muscle, three electrodes will be used; two electrodes will be placed ~30 mm apart in the direction of the muscle fibers and a ground electrode will be placed over the closest bony prominence. Before placement of the electrodes, the subject's skin will be cleaned with alcohol to reduce impedance and excess hair will be removed to eliminate shifting of the electrodes if needed. The stair-stepping task consists of descending 2 steps. Patients should start descending the steps immediately in response to a command, at their normal speed with their affected limb. Healthy subjects should start descending stairs with their dominant limb . Before data acquisition, participants should perform one practice trial of stair descent to get familiarized with the task. Then the participants should perform three test trials with thirty seconds of rest after each trial to prevent fatigue. The raw data will be stored on a personal computer for analysis with a custom program in Matlab (Math Works, Natick, Massachusetts, USA). Investigators should use a mean of data in three trials for analysis. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT05407077
Study type Observational
Source Cairo University
Contact
Status Completed
Phase
Start date June 30, 2022
Completion date January 2, 2023

See also
  Status Clinical Trial Phase
Completed NCT01434966 - Changes in Quadriceps Function Following Local or Distant Interventions in Individuals With Patellofemoral Pain N/A
Completed NCT04796103 - The Effectiveness of Prolotherapy (%5 Dextros) in the Treatment of Patients With Chondromalacia Patella N/A
Not yet recruiting NCT05597670 - Effect of Proximal Stabilization on Recruitment of the Core & Vasti in Patellofemoral Arthritis During Descending Stairs N/A
Completed NCT04669834 - Effect of Core Stability Exercise on Isolated Patellofemoral Osteoarthritis. N/A
Completed NCT03515720 - Neuroprolotherapy With Physical Therapy for Treatment of Patellar Chondromalacia N/A
Recruiting NCT05096520 - Intermedius Genicular Nerve in the Treatment of Patients With Chondromalacia Patella N/A
Completed NCT04589702 - Temporal Activation of Core Muscles and Vasti in Isolated Patellofemoral Osteoarthritis
Completed NCT06020794 - The Efficacy of LPPRP in the Treatment of Chondromalacia Patella N/A