- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT03954301
Using the Hierarchical Cluster Method for Foot Deformities (Cluster)
Anthropometric and Biomechanical Variables Causing Foot Deformities in Young Individuals, Using the Hierarchical Cluster Method
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
Aim and Introduction: Due to individual anthropometric differences, there are many different types of foot posture Foot posture variations affect lower extremity structure, alignment and biomechanical characteristics. Particularly in younger people, performing critical biomechanical measurements in the lower extremity and foot is extremely important to the detection of, and early intervention in, orthopedic problems that these individuals will encounter in their later life. In the literature, attempts at analysis of the evaluations realized so far have been made by univariate analysis. Considering the relationship between variation and variables, these methods result in loss of information. The aim of this study is to analyze all of the variables with a Hierarchical Cluster Analysis of Multivariate Statistical Methods to obtain more sensitive results, and also to add a new dimension to the hypothesis included in the study.
Methods: The study is carried out on 2nd and 3rd year university students in the physiotherapy and rehabilitation department taking a kinesiology course. The analyses are performed at the Biruni University Physiotherapy and Rehabilitation laboratory. Patients with musculoskeletal system pathomechanics which could prevent standing and walking are not included in the study. After demographic characteristics are recorded, Q, valgity angle, subtalar joint, medial longitudinal arch and hallux valgus angles are measured with a goniometer. The height from the ground of the navicula are calculated by caliper, using the Navicular drop test. Metatarsal width are also calculated with this device. Medial longitudinal arch angle, metatarsal width and nacivular drop tests are performed under weight-bearing and non-weight-bearing conditions.
Study Type
Enrollment (Actual)
Contacts and Locations
Study Locations
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-
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Istanbul, Turkey
- Başar Öztürk
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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:
- Healthy university students.
- Must be able to walk independently.
Exclusion Criteria:
- Students with chronic sprains.
- Students who had undergone lower extremity surgery within the last year.
- Students who use assistive walking devices.
Study Plan
How is the study designed?
Design Details
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Navicular drop test
Time Frame: 2 weeks.
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The height of navicula will be measured in weight-bearing and non-weight bearing conditions in millimeters.
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2 weeks.
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Metatarsal width
Time Frame: 2 weeks.
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The width of metatarsal zone will be measured in weight-bearing and non-weight bearing conditions in millimeters.
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2 weeks.
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Subtalar angle
Time Frame: 2 weeks.
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The angle between calcaneus and Achilleus tendon will be measured with goniometer in standing position and the degree will be calculated.
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2 weeks.
|
Hallux valgus angle
Time Frame: 2 weeks.
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The angle between 1st metatars and hallux will be measured with goniometer and the degree will be calculated.
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2 weeks.
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Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Q angle
Time Frame: 2 weeks.
|
The angle of quadriceps femoris muscle will be measured with goniometer in supine position and the degree will be assessed.
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2 weeks.
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Medial longitudinal arch angle
Time Frame: 2 weeks.
|
The angle between 1st metatarsophalangeal joint, navicula and medial malleol will be measured and the degree will be calculated.
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2 weeks.
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Collaborators and Investigators
Sponsor
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
- BiruniUni
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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