- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT03685812
Validity and Reliability of Autocad Software Assessment of JPS in PFPS
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:
- To assess the intra-tester and between day reliability of measurement of JPS using Autocad software.
- To assess the validity of these measurements against those found during an IKD.
Study Overview
Status
Conditions
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
Enrollment (Actual)
Contacts and Locations
Study Locations
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Giza, Egypt, egypt
- Faculty of physical therapy, Cairo University
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Sampling Method
Study Population
Description
inclusion criteria:
- 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
- Insidious onset of symptoms unrelated to a traumatic incident.
- 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.
- Patient with chronic PFPS (pain > 3 months)
Exclusion Criteria:
- Meniscal or other intraarticular pathologic conditions; cruciate or collateral ligament involvement.
- A history of traumatic patellar subluxation or dislocation.
- Previous surgery in the knee, ankle and hip joints.
- Knee, ankle and hip joints osteoarthritis.
athletes weren't included.
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Study Plan
How is the study designed?
Design Details
Cohorts and Interventions
Group / Cohort |
Intervention / Treatment |
|---|---|
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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.
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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:
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
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Concurrent validity of Autocad software
Time Frame: one day
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correlation between absolute angular error of Autocad software and isokinetic system
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one day
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Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
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Intrarater reliability of
Time Frame: 48 hours
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same investigator will repeat joint positsion sense by Autocad software
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48 hours
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Collaborators and Investigators
Sponsor
Investigators
- Principal Investigator: karima A Hassan, Cairo university
Publications and helpful links
General Publications
- Drouin JM, Valovich-mcLeod TC, Shultz SJ, Gansneder BM, Perrin DH. Reliability and validity of the Biodex system 3 pro isokinetic dynamometer velocity, torque and position measurements. Eur J Appl Physiol. 2004 Jan;91(1):22-9. doi: 10.1007/s00421-003-0933-0. Epub 2003 Sep 24.
- Relph N, Herrington L. Criterion-related validity of knee joint-position-sense measurement using image capture and isokinetic dynamometry. J Sport Rehabil. 2015 Jan 13;24(1):2013-0119. doi: 10.1123/jsr.2013-0119. Print 2015 Feb 1.
- Bolgla LA, Boling MC. An update for the conservative management of patellofemoral pain syndrome: a systematic review of the literature from 2000 to 2010. Int J Sports Phys Ther. 2011 Jun;6(2):112-25.
- Akseki D, Akkaya G, Erduran M, Pinar H. [Proprioception of the knee joint in patellofemoral pain syndrome]. Acta Orthop Traumatol Turc. 2008 Nov-Dec;42(5):316-21. doi: 10.3944/aott.2008.316. Turkish.
- Baker V, Bennell K, Stillman B, Cowan S, Crossley K. Abnormal knee joint position sense in individuals with patellofemoral pain syndrome. J Orthop Res. 2002 Mar;20(2):208-14. doi: 10.1016/S0736-0266(01)00106-1.
- Mir SM, Hadian MR, Talebian S, Nasseri N. Functional assessment of knee joint position sense following anterior cruciate ligament reconstruction. Br J Sports Med. 2008 Apr;42(4):300-3. doi: 10.1136/bjsm.2007.044875.
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- Patellofemoral Pain syndrome
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
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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