Validity and Reliability of Autocad Software Assessment of JPS in PFPS

March 28, 2019 updated by: Karima Abdelaty Hassan, Cairo University

Validity and Reliability of Autocad Software Assessment of Joint Position Sense in Patellofemoral Pain Syndrome

The overall aim of the study is to assess the reliability and validity of Autocad software to measure JPS in PFPS, especially:

  1. To assess the intra-tester and between day reliability of measurement of JPS using Autocad software.
  2. To assess the validity of these measurements against those found during an IKD.

Study Overview

Status

Completed

Intervention / Treatment

Detailed Description

Patellofemoral pain syndrome (PFPS) is a common painful musculoskeletal condition that affects physically active young adults and adolescents.

Joint position sense (JPS) is considered as a component of proprioception as it provides the clinician with information regarding the accuracy of movement as well as its relationship with movement performance and injuries. Therefore researchers use advanced instruments as 3 D video systems and isokinetic dynamometer. Since these instruments are less portable and expensive, therefore researchers used another method to evaluate JPS using high precision software using video analysis and markers in the joints. Unfortunately, video analysis requires difficult and time-consuming tasks and that this slow the evaluation process.

Although immediate feedback could help physiotherapists and athletic trainers to monitor athletes and make decisions during the training session and the rehabilitation process, such immediacy is not available for proprioceptive tests in field situations. Autocad software is available and inexpensive and provides immediate feedback

Study Type

Observational

Enrollment (Actual)

38

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

      • Giza, Egypt, egypt
        • Faculty of physical therapy, Cairo 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

18 years to 35 years (Adult)

Accepts Healthy Volunteers

No

Genders Eligible for Study

All

Sampling Method

Non-Probability Sample

Study Population

thirty-eight patients(males and females) with PFPS will be recruited from the outpatient clinic of the faculties of Physical Therapy, Cairo University, Egypt.

Description

inclusion criteria:

  1. Anterior or retropatellar knee pain from at least 2 of the following Activities : (1) prolonged sitting; (2) stair climbing; (3) squatting; (4) running; (5) kneeling; (6) hopping/jumping; (7) kneel sitting
  2. Insidious onset of symptoms unrelated to a traumatic incident.
  3. Age of the subject 18-35 years to limit the possibility that PFPS over age 35 may have been complicated by arthritic changes, and also the subjects should have closed epiphyseal growth plates.
  4. Patient with chronic PFPS (pain > 3 months)

Exclusion Criteria:

  1. Meniscal or other intraarticular pathologic conditions; cruciate or collateral ligament involvement.
  2. A history of traumatic patellar subluxation or dislocation.
  3. Previous surgery in the knee, ankle and hip joints.
  4. Knee, ankle and hip joints osteoarthritis.
  5. athletes weren't included.

    -

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
patients with patellofemoral pain syndrome , Auto Cad software
Patients referred with a confirmed diagnosis of patellofemoral pain syndrome, with a visual analogue scale of more than 3. Anterior or retropatellar 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.
The participants will be prepared for image-capture data collection by putting four squared markers on leg and thigh.Each subject will extend his/her leg and make two angles from the resting position (90º) to the full extension, photos will be taken. The tested leg passively moved by the researcher through 20° to 60° of knee extension, the participant will be instructed to actively move that leg to the target angle and hold it in this position another photograph will be taken. The angles will be measured using the AutoCAD software. Knee JPS measurements will also be collected using an IKD by same steps
Other Names:
  • Isokinetic system

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Concurrent validity of Autocad software
Time Frame: one day
correlation between absolute angular error of Autocad software and isokinetic system
one day

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Intrarater reliability of
Time Frame: 48 hours
same investigator will repeat joint positsion sense by Autocad software
48 hours

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Investigators

  • Principal Investigator: karima A Hassan, Cairo university

Publications and helpful links

The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.

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)

September 25, 2018

Primary Completion (Actual)

February 1, 2019

Study Completion (Actual)

February 1, 2019

Study Registration Dates

First Submitted

September 24, 2018

First Submitted That Met QC Criteria

September 24, 2018

First Posted (Actual)

September 26, 2018

Study Record Updates

Last Update Posted (Actual)

April 1, 2019

Last Update Submitted That Met QC Criteria

March 28, 2019

Last Verified

March 1, 2019

More Information

Terms related to this study

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

NO

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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