Effect of Hip Adductors Isometric Contraction on Knee Extensors Isokinetic Torque in Patellofemoral Pain Syndrome

Sponsor
Badr University (Other)
Overall Status
Not yet recruiting
CT.gov ID
NCT05083897
Collaborator
Cairo University (Other)
30
2

Study Details

Study Description

Brief Summary

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

Condition or Disease Intervention/Treatment Phase
  • Other: hip adduction isometric contraction

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 Design

Study Type:
Observational
Anticipated Enrollment :
30 participants
Observational Model:
Other
Time Perspective:
Cross-Sectional
Official Title:
Effect of Hip Adductors Isometric Contraction on Knee Extensors Isokinetic Torque in Patellofemoral Pain Syndrome
Anticipated Study Start Date :
Oct 1, 2021
Anticipated Primary Completion Date :
Nov 1, 2021
Anticipated Study Completion Date :
Dec 1, 2021

Arms and Interventions

Arm Intervention/Treatment
30 patients in 1 group

measuring the effect of isometric hip adduction with knee extension on the peak torque of knee extensors

Other: hip adduction isometric contraction
addition of isometric hip adduction contraction to the knee extension for measuring knee extension peak torque by the isokinetic dynamometer

Outcome Measures

Primary Outcome Measures

  1. peak torque of knee extensors [2 months]

    the maximum rotatory force that can be generated by the knee extensor muscles measured by the isokinetic dynamometer

  2. pain level at the patellofemoral area [2 months]

    pain will be measured around the patellofemoral area by the visual analogue scale

  3. hip adduction peak torque [2 months]

    hip adduction maximum rotatory force measured by the hand held dynamometer

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years to 35 Years
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
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.

Contacts and Locations

Locations

No locations specified.

Sponsors and Collaborators

  • Badr University
  • Cairo University

Investigators

None specified.

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Yasmine Ramadan, teaching assistant, Badr University
ClinicalTrials.gov Identifier:
NCT05083897
Other Study ID Numbers:
  • yasmine zaki
First Posted:
Oct 19, 2021
Last Update Posted:
Oct 19, 2021
Last Verified:
Oct 1, 2021
Individual Participant Data (IPD) Sharing Statement:
Undecided
Plan to Share IPD:
Undecided
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Keywords provided by Yasmine Ramadan, teaching assistant, Badr University
Additional relevant MeSH terms:

Study Results

No Results Posted as of Oct 19, 2021