Reliability and Validity of the Surgimap Software for Measuring Quadriceps Angle in Healthy Subjects
1 other identifier
observational
20
1 country
1
Brief Summary
The purpose of this study is to investigate the intra- and inter-rater reliability and concurrent validity of surgimap software for measuring the Q angle Surgimap (Nemaris Inc, New York, NY, USA) is a dedicated spine measurement and surgical planning software which is used in both the research works and the clinical rehabilitation. Q angle is considered to be an index of the vector for action of the patellar tendon and extensors mechanism which is highly affects the patellofemoral joint dysfunction and foot mechanics.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at below P25 for all trials
Started Aug 2023
Shorter than P25 for all trials
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
First Submitted
Initial submission to the registry
August 19, 2023
CompletedFirst Posted
Study publicly available on registry
August 24, 2023
CompletedStudy Start
First participant enrolled
August 30, 2023
CompletedPrimary Completion
Last participant's last visit for primary outcome
January 30, 2024
CompletedStudy Completion
Last participant's last visit for all outcomes
January 30, 2024
CompletedFebruary 20, 2024
February 1, 2024
5 months
August 19, 2023
February 19, 2024
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
The inter-rater, intra-rater reliability and concurrent validity of the surgimap software for measuring the Q-angle.
the accuracy and consistency of surgimap software for measuring the q angle
3 months
Interventions
20 healthy subjects will be recruited in the study, the q angle will be measured using goniometer and surgimap soft ware, 3 examiners will measure the q angles for the same individuals to check the inter rater reliability, and the test will be repeated after 2 days by the same examiners to check the intra rater reliability
Eligibility Criteria
This study will be conducted in the out-patient clinic Faculty of physical therapy, Cairo University. The expected duration to recruit patients and collect data is 3 months .
You may qualify if:
- Both male \& female
- Aged 18:25
- BMI 18.5: 25
- Normal foot posture as assessed by foot posture index.
You may not qualify if:
- Subjects who have operations in the knee joint
- Subjects who have traumatic knee injury
- High arched or low arched foot.
Contact the study team to confirm eligibility.
Sponsors & Collaborators
- Cairo Universitylead
Study Sites (1)
Faculty of physical therapy, Cairo University
Giza, 11432, Egypt
Study Officials
- PRINCIPAL INVESTIGATOR
Aida Nassif, PHD
lecturer of physical therapy, Cairo University
Study Design
- Study Type
- observational
- Observational Model
- OTHER
- Time Perspective
- CROSS SECTIONAL
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Lecturer
Study Record Dates
First Submitted
August 19, 2023
First Posted
August 24, 2023
Study Start
August 30, 2023
Primary Completion
January 30, 2024
Study Completion
January 30, 2024
Last Updated
February 20, 2024
Record last verified: 2024-02