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Completed

NCT Number: NCT03629938

Evaluation and Classification of Foot Medial Longitudinal Arch Height in Adults

The aim of the study is, to evaluate and classificate the medial longitudinal arch height in adult individuals. Aged between 18-40 years,350 adults who are voluntarily participate is going to be evaluate with Feiss Line(FL), Navicular Drop(ND) and Longitudinal Arch Angle(LAA) in subtalar neutral and resting position. Maximum, minimum values are going to be calculated. The 95% and 68% prediction intervals will be used as cut off limits.

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Key information

About this study

The aim of the study is, to evaluate and classificate the medial longitudinal arch height in adult individuals.

Aged between 18-40 years,350 adults who are voluntarily participate is going to be evaluate with Feiss Line(FL), Navicular Height(NH) and Longitudinal Arch Angle(LAA) in subtalar neutral and resting position. Maximum, minimum values are going to be calculated.

Participant's height, weight and foot length, from posterior aspect of calcaneus to the longest toe's tip, will be measured. Center of the medial malleolus, the navicular tuberosity and the head of the first metatarsal bone will be marked with a CD marker. With these landmarks in foot's relaxed position, neutrally, FL, NH and LAA will be measured by a ruler.

Feiss Line is a drawn line between the center of the medial malleolus to the head of the first metatarsal bone and then perpendicular line distance between this line and the navicular tuberosity will be drawn.The vertical line between the ground and the tubercle indicates Navicular Height. Center of goniometer placed at the navicular tuberosity then goniometer arms follow the medial malleolus and the head of the first metatarsal bone, degree between two arms indicates Longitudinal Arch Angle.

FL, NH, LAA mean values will be calculated. The 95% and 68% prediction intervals will be used as cut off limits.

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Being between the ages of 18-40
  • Individuals who voluntarily agree to participate in the study

Exclusion criteria

  • Those who have foot operation
  • Foot trauma story which is causing an anatomic disorder

Treatment and study plan

Evaluation

Other

evaluation and classification of medial longitudinal arch height of foot in adults

Primary outcomes

  1. Medial longitudinal arch height

    Time frame: 10 days

    Navicular Height(NH) mean value, Center of the medial malleolus, the navicular tuberosity and the head of the first metatarsal bone will be marked with a CD marker. With these landmarks in foot's relaxed position, neutrally NH will be measured by a ruler.

    The vertical line between the ground and the tubercle indicates Navicular Height. After all data collection, the data will be entered into the Statistical Package for the Social Sciences (SPSS) and the average value calculated.

Secondary outcomes

  1. Mean value differences between male and female

    Time frame: 10 days

    Mean value differences between male and female will be compared statistically with the Statistical Package for the Social Sciences (SPSS) program.

  2. Correlation of arc measurements and standing length

    Time frame: 10 days

    Correlation of arc measurements and standing length will be correlated statistically with the Statistical Package for the Social Sciences (SPSS) program.

  3. Medial Longitudinal Arch Cut Off Values

    Time frame: 10 days

    After average values calculated, cut off values will be generated from the data obtained from the arch height in standard, healthy individuals.

Sponsors and collaborators

Lead sponsor

Istanbul Medipol University Hospital

Other

Registry information

Official study title

Erişkinlerde Ayak Medial Longitudinal Ark Yüksekliğinin Değerlendirilmesi ve Sınıflandırılması

Important dates

Study start
2019
Primary completion
2019
Study completion
2019
First posted
Aug 14, 2018
Registry last updated
Jul 29, 2020

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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