Effect of Proximal Stabilization on Recruitment of the Core & Vasti in Patellofemoral Arthritis During Descending Stairs

Chondromalacia Patellae Clinical Trial

Official title:

Effect of Proximal Stabilization on Recruitment of the Core & Vasti in Patients With Patellofemoral Arthritis as They Descend Stairs

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT05597670
• Other study ID #: P.T.REC/012/003438
• Status: Completed
• Phase: N/A
• Start date: November 29, 2022
• Est. completion date: June 1, 2024

Study information

• Verified date: June 2024
• Source: Cairo University
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

Purpose: to investigate the effect of proximal stability on PF OA. Methods: Thirty patients with PF OA will be recruited. Patients will be randomly assigned into two groups, group A and group B . Patients in both groups will receive a traditional physical therapy treatment, but group (B) will receive additional proximal stability exercise. All patients will be evaluated for muscular recruitment strategies (onset and duration) of multifidus, transversus abdominus (TrA), gluteus medius (GM), and vasti measured by quantitative Electromyography during stair descent. pre and post-treatment.

Description:

: A) Procedures for evaluation: The practical section of the studywill be undertaken in 6 weeks (2 sessions a week). Measurement will be taken before the start of treatment program then after the end of 6 weeks treatment program. 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 stairstepping task will consist of descending 2 steps Before data acquisition, participants will be asked to perform one practice trial of stair descent to get familiarized with the task. Then the participants will 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 . Investigators will use a mean of data in three trials for analysis.

b) Procedures for treatment: All patients will receive a traditional physical therapy program in the form of TENS , stretching hamstring, quadriceps and calf muscles

• Group (A) Patients in this group will receive a traditional therapeutic knee rehabilitation program in the form of mini-squatting exercise (up to 45 degrees knee flexion measured by a universal goniometer) , strengthening of hip abductors and external rotators using clamshell exercise . No emphasis will be placed on stabilizing the core musculature before initiating any of those exercises.

• Group (B) Patients in this group will receive the same program as group (A) plus proximal stability exercise and the principles of proximal stability will be explained to patients before initiation of treatment and patients will be asked to comply with these principles during exercise. These principles include learning how to activate transversus abdominus by abdominal bracing without allowing pelvis tilting and ensure neutral spine and diaphragmatic breathing during exercise.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 50
• Est. completion date: June 1, 2024
• Est. primary completion date: June 1, 2024
• Accepts healthy volunteers: No
• Gender: Female
• Age group: 35 Years to 55 Years

Eligibility

Inclusion Criteria:

1. Anterior- or retro-patellar knee pain aggravated by at least two activities that load the PFJ (eg; stair ambulation, squatting and/or rising from sitting) .

2. Pain during these activities presented on most days during the past month and their pain severity was = 4 on an 11 point numerical pain scale during aggravating activities .,

3. A grade less than (2) from postero-anterior views on the Kellgren - Lawrence (KL) grading scale.

Exclusion Criteria:

1. concomitant pain from tibiofemoral joint or other knee structures .

2. current or previous pain in the hip, lumbar spine or foot that had lasted longer than 3 months and/or required intervention.

3. a history of lower extremity, pelvis or spine fractures; spine, hip, knee or foot surgeries; hip or patellar subluxation/ dislocation.

4. injury to any of knee ligaments or meniscus.

5. systemic diseases (e.g. rheumatoid arthritis), neurological conditions or fibromyalgia .

6. The professional athletes; people who exercise more than two hours a day or every other day, will be excluded.

Related Conditions & MeSH terms

• Cartilage Diseases
• Chondromalacia Patellae

Intervention

Other:
• traditional knee rehabilitation program
Patients in this group will receive a traditional therapeutic knee rehabilitation program in the form of mini-squatting exercise (up to 45 degree knee flexion measured by a universal goniometer) , strengthening of hip abductors and external rotators
• proximal stabilization
the principles of proximal stability will be explained to patients before initiation of treatment and patients will be asked to comply with these principles during exercise. These principles include learning how to activate transversus abdominus by abdominal bracing without allowing pelvis tilting and ensure neutral spine and diaphragmatic breathing during exercise.

Locations

Country	Name	City	State
Egypt	faculty of physical therapy, Cairo university	Giza

Sponsors (1)

Lead Sponsor	Collaborator
Cairo University

Country where clinical trial is conducted

Egypt, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	The change of EMG onset of multifidus	investigators will collect the EMG activity of multifidus by electromyography (EMG) using surface electrodes	baseline and six weeks
Primary	The change of EMG duration of multifidus	investigators will collect the EMG activity of multifidus by electromyography (EMG) using surface electrodes	baseline and six weeks
Primary	The change of EMG duration of vastus medialis obliqus	investigators will collect the EMG activity of vastus medialis obliqus by electromyography (EMG) using surface electrodes	baseline and six weeks
Primary	The change of EMG onset of vastus medialis obliqus	investigators will collect the EMG activity of vastus medialis obliqus by electromyography (EMG) using surface electrodes	baseline and six weeks
Primary	The change of EMG onset of vastus lateralis	investigators will collect the EMG activity of vastus lateralis by electromyography (EMG) using surface electrodes	baseline and six weeks
Primary	The change of EMG duration of vastus lateralis	investigators will collect the EMG activity of vastus lateralis by electromyography (EMG) using surface electrodes	baseline and six weeks
Primary	The change of EMG duration of gluteus medius	investigators will collect the EMG activity of gluteus medius by electromyography (EMG) using surface electrodes	baseline and six weeks
Primary	The change of EMG onset of gluteus medius	investigators will collect the EMG activity of gluteus medius by electromyography (EMG) using surface electrodes	baseline and six weeks
Primary	The change of EMG onset of transversus abdominus	investigators will collect the EMG activity of transversus abdominus by electromyography (EMG) using surface electrodes	baseline and six weeks
Primary	The change of EMG duration of transversus abdominus	investigators will collect the EMG activity of transversus abdominus by electromyography (EMG) using surface electrodes	baseline and six weeks
Secondary	kinesiophobia	patients will respond to the questions of the Tempa scale	baseline and six weeks