- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05083897
Effect of Hip Adductors Isometric Contraction on Knee Extensors Isokinetic Torque in Patellofemoral Pain Syndrome
October 6, 2021 updated by: Yasmine Ramadan, Badr University
the study will be done to investigate the effect of hip adduction isometric contraction on the pain level by VAS and knee extensors peak torque by using the isokinetic dynamometer in patients with unilateral patellofemoral pain syndrome
Study Overview
Status
Not yet recruiting
Conditions
Intervention / Treatment
Detailed Description
the study will be done to investigate the effect of isometric hip adduction that will be measured by the hand held dynamometer (the manual muscle tester) to measure the produced adduction torque and its effect on the peak torque of knee extension by the knee extensors which will be measured by the isokinetic dynamometer in addition to measuring the pain intensity before and through the assessment by using the visual analogue scale
Study Type
Observational
Enrollment (Anticipated)
30
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Contact
- Name: yasmin zaki, Bsc
- Phone Number: 01155667664
- Email: doc_yasminezaki23@yahoo.com
Study Contact Backup
- Name: mohamed gamal, Phd
- Phone Number: 01122712777
- Email: mohamed.hassan@gaf.edu.eg
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
18 years to 35 years (ADULT)
Accepts Healthy Volunteers
No
Genders Eligible for Study
All
Sampling Method
Probability Sample
Study Population
patients suffering from unilateral patellofemoral pain syndrome
Description
Inclusion Criteria:
- Anterior or retro-patellar knee pain from at least 2 of the following Activities: (1) prolonged sitting; (2) stair climbing; (3) squatting; (4) running; (5) kneeling; and (6) hopping/jumping (Tyler et al., 2006).
- Insidious onset of symptoms unrelated to a traumatic incident and persistent for at least 6 weeks (subacute or chronic pain).
- They will be diagnosed as a PFPS case by a physician
- The patient's age will be ranged from 18-35 years to limit the possibility that PFPS over age 35 may have been complicated by arthritic changes, and also the patients should have closed epiphyseal growth plates (Robinson and Nee, 2007).
Exclusion Criteria:
- A history of any of the following condition: meniscal or other intra articular pathologic conditions; cruciate or collateral ligament involvement.
- A history of traumatic patellar subluxation or dislocation.
- Previous surgery in the knee and hip joints.
- Any lower limb bony/congenital deformity.
- Ankle, Knee and hip joints osteoarthritis.
- A history of any conditions affects muscle strength: diabetes mellitus, rheumatoid arthritis.
- Pregnancy.
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
Cohorts and Interventions
Group / Cohort |
Intervention / Treatment |
|---|---|
|
30 patients in 1 group
measuring the effect of isometric hip adduction with knee extension on the peak torque of knee extensors
|
addition of isometric hip adduction contraction to the knee extension for measuring knee extension peak torque by the isokinetic dynamometer
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
peak torque of knee extensors
Time Frame: 2 months
|
the maximum rotatory force that can be generated by the knee extensor muscles measured by the isokinetic dynamometer
|
2 months
|
|
pain level at the patellofemoral area
Time Frame: 2 months
|
pain will be measured around the patellofemoral area by the visual analogue scale
|
2 months
|
|
hip adduction peak torque
Time Frame: 2 months
|
hip adduction maximum rotatory force measured by the hand held dynamometer
|
2 months
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Collaborators
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 (ANTICIPATED)
October 1, 2021
Primary Completion (ANTICIPATED)
November 1, 2021
Study Completion (ANTICIPATED)
December 1, 2021
Study Registration Dates
First Submitted
October 6, 2021
First Submitted That Met QC Criteria
October 6, 2021
First Posted (ACTUAL)
October 19, 2021
Study Record Updates
Last Update Posted (ACTUAL)
October 19, 2021
Last Update Submitted That Met QC Criteria
October 6, 2021
Last Verified
October 1, 2021
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- yasmine zaki
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
UNDECIDED
IPD Plan Description
the outcomes can be used in future researches concerning this field of interest
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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-
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