- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06758050
Effect of Core Exercises on Patellofemoral Pain Syndrome
Effect of Adding Core Exercises to Hip and Knee-focused Exercises on Patellofemoral Pain Syndrome
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
Purpose: Patellofemoral pain syndrome is a frequent musculoskeletal disorder, which can result from core muscles instability that can lead to pain, function and altered dynamic balance. The objective of this study is to assess the effect of core muscle strengthening on pain, function, strength and dynamic balance in patients with patellofemoral pain syndrome.
Subjects and Methods: Forty-four patients with age ranging from 18 to 35 years with patellofemoral pain syndrome will be divided into study (N=22) and control (N=22) groups. Both groups will be given 6 weeks of conventional physical therapy program and an additional core muscle strengthening for the study group. The tools are being used to assess the outcome are 1- Visual Analogue Scale,2- handheld dynamometer,3-AKPS 4- BIODEX Balance.
Hypotheses:
It will be hypothesized that:
- There is no effect of core strengthening exercises on pain in treating PFPS.
- There is no effect of core strengthening exercises on muscle strength in treating PFPS.
- There is no effect of core strengthening exercises on function in treating PFPS.
Study Type
Enrollment (Estimated)
Phase
- Not Applicable
Contacts and Locations
Study Contact
- Name: Rana Ibrahim Ahmed, Bachelor Physical Therapy-MUST
- Phone Number: 01151082787
- Email: ranaibrahim066@gmail.com
Study Locations
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-
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Giza, Egypt
- Recruiting
- Cairo University
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Contact:
- Rana Ibrahim, Bachelor
- Phone Number: 01151082787
- Email: ranaibrahim066@gmail.com
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-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Adult
Accepts Healthy Volunteers
Description
Inclusion Criteria:
- Patients of both genders with an age range of 18- 35 years old.
- Gradual development of pain in the front of the knee lasting more than 12 weeks.
- Patients with body mass index 18- 25 kg m2.
Pain is aggravated by at least 2 of the following activities: jumping, running, prolonged sitting, stair climbing, kneeling, and squatting.
- Positive patellar grinding test.
- Insidious onset of symptoms, unrelated to a traumatic damage.
Exclusion Criteria:
- Traumatic patellar subluxation or dislocation.
- A history of any of the following conditions: meniscal or other intra articular pathologic conditions; cruciate or collateral ligament involvement.
- Any lower limb bony or congenital deformities.
- Previous knee and hip joint surgeries.
- Osteoarthritis in the ankle, knee, or hip joints.
- Conditions that affect muscle strength such as diabetes mellitus or rheumatoid arthritis.
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Treatment
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Study group
Group B (study group) (core strengthening exercises added to evidence-based approaches group) The core muscle strength training program The core muscle strength training program will last for 6 weeks and comprise of two training sessions per week, with a total of 12 sessions for the study group. During the main part of the training, the "big 3" exercises as described by McGill will be conducted. These include the curl-up, side bridge, and quadruped position. |
By core strengthening exercise, could be improved pain, balance, and function in patients with patellofemoral pain syndrome.
In that case, this will not only improve their postural stability and neuromuscular control, but we believe it will improve their overall functional, performance, and quality of life.
Currently, limited evidence exists about the effectiveness of core strengthening exercises on pain, function and dynamic balance in patellofemoral pain syndrome.
By addressing core strengthening exercise, physical therapists can advise new treatment methods for patellofemoral pain syndrome (Chevidikunnan et al., 2016)
hip and knee-focused exercises
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|
Active Comparator: Control group
Group A (control group) (evidence-based approaches group): The participants in the control group will receive only a hip and knee- focused exercise program.
|
hip and knee-focused exercises
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Pain
Time Frame: 6 weeks
|
by Visual analog scale
|
6 weeks
|
|
knee function
Time Frame: 6 weeks
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by Anterior knee pain scale ( AKPS) ( Kujala )
|
6 weeks
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Muscle strength
Time Frame: 6 weeks
|
By hand held dynamometer
|
6 weeks
|
|
Balance
Time Frame: 6 weeks
|
By Biodex balance system
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6 weeks
|
Collaborators and Investigators
Sponsor
Investigators
- Principal Investigator: rana ibrahim ahmed, Bachelor Physical Therapy-MUST, Misr University for Science and Technology
- Study Chair: Nasr Awad Abd Elkader, Assistant Professor, Physical Therapy for Musculoskeletal Disorders and its Surgeries Faculty of Physical Therapy Cairo University
- Study Director: Abdelgalil Allam Abdelgalil, Lecturer of Physical Therapy, Physical Therapy for Musculoskeletal Disorders and its Surgeries Faculty of Physical Therapy Cairo University
- Study Director: Mohammed Safwat Hamza, Associate Professor, Faculty of Medicine Misr University for Science and Technology
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Estimated)
Study Completion (Estimated)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- No:P.T.REC/012/005347
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
Clinical Trials on Patellofemoral Pain Syndrome
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