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

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

    • Al Riyadh
      • Al Majma'ah, Al Riyadh, Saudi Arabia, 11952
        • Rehabilitation center, Majmaah University

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
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
6 weeks
Pain intensity
Time Frame: 6 weeks
investigated for their current intensity of pain on a Visual analogue scale 0 to 10 scale.
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.

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

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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