- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05168332
The Effect of Patellar Taping and Isometric Strength Training on Quadriceps Strength With Patellofemoral Pain Syndrome.
March 14, 2024 updated by: Shahnaz Hasan, PhD, Majmaah University
The Influence of Patellar Taping Combined With Isometric Strength Training on Pain, Muscle Strength, and Functional Performance in Individuals With Patellofemoral Pain Syndrome.
Patellofemoral pain syndrome is one of the most common young adult female complaints, caused by changes in the patellofemoral joint's physical and biomechanical properties.
This study compared the Short-term effects of patellar taping combined with isometric contraction of quadriceps muscle strengthening at 900 or 600 knee angles on quadriceps strength and functional performance in a female patient with patello-femoral pain syndrome (PFPS)
Study Overview
Status
Completed
Conditions
Detailed Description
Quadriceps muscle strength Pain intensity Knee function
Study Type
Interventional
Enrollment (Actual)
60
Phase
- Not Applicable
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
-
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Al Riyadh
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Al Majma'ah, Al Riyadh, Saudi Arabia, 11952
- Rehabilitation center, Majmaah University
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Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
25 years to 40 years (Adult)
Accepts Healthy Volunteers
No
Description
Inclusion Criteria:
- knee pain for at least eight weeks that was aggravated by activities such as descending and ascending stairs, squatting, and running.
- knee pain with a positive J sign (lateral tilt of patella)
- more symptomatic and mal align knee included in case of bilateral involvement and a sign of patellar malalignment on the radiograph.
Exclusion Criteria:
- History of knee fracture
- Patella dislocation
- knee deformity (e.g., genu varum)
- Knee Flexion contracture
- Ligament/meniscal injuries,
- NSAID or intra-articular injection, or knee Osteo arthritis.
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Primary Purpose: Treatment
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Single
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
---|---|
Experimental: Experimental(Group A): patellar taping combined with isometric strength training
The experimental group (Group A): patellar taping with isometric strength training for six weeks.
|
patellar taping combined with isometric strength training
sham patellar taping combined with isometric strength training
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Sham Comparator: Control group (Group B): sham patellar taping combined with isometric strength training.
Control group (Group B): sham patellar taping combined with isometric strength training for six weeks.
|
patellar taping combined with isometric strength training
sham patellar taping combined with isometric strength training
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Quadriceps muscle strength
Time Frame: 6 weeks
|
Knee extensors (Maximal Voluntary Isometric Contraction) strength (STN) test at 60, and 90 degrees angles
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6 weeks
|
Pain intensity
Time Frame: 6 weeks
|
investigated for their current intensity of pain on a Visual analogue scale 0 to 10 scale.
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6 weeks
|
Knee function
Time Frame: 6 weeks
|
Knee function will be assessed using the validated Kujala Anterior Knee Pain scale
|
6 weeks
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Investigators
- Principal Investigator: Shahnaz Hasan, PhD, Associate Professor, Majmaah University
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (Actual)
December 5, 2021
Primary Completion (Actual)
June 26, 2022
Study Completion (Actual)
September 25, 2022
Study Registration Dates
First Submitted
December 12, 2021
First Submitted That Met QC Criteria
December 12, 2021
First Posted (Actual)
December 23, 2021
Study Record Updates
Last Update Posted (Actual)
March 15, 2024
Last Update Submitted That Met QC Criteria
March 14, 2024
Last Verified
March 1, 2024
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- S.Hasan
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
UNDECIDED
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
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.
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