MedTrace Logo

Validation of the American Orthopedic Foot and Ankle Society Midfoot Scale

NCT05246488 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 57

Last updated 2022-09-29

No results posted yet for this study

Summary

Today, one of the frequently used scales in the evaluation of foot problems is the American Orthopedic Foot and Ankle Association Scale. AOFAS has been prepared with the American society in mind and its original version is in English. This limits the application of AOFAS to non-English speaking patients. The aim of study is to investigate the cross-cultural adaptation, reliability and validity of the Turkish version of the AOFAS Midfoot Scale.

Conditions

  • Foot

Interventions

DIAGNOSTIC_TEST

American Orthopedic Foot and Ankle Association Midfoot Scale, Foot and Ankle Ability Measure/FAAM, SF-12 Quality of Life Scale, Visual Analog Scale (VAS)

All participants will receive two assessments, 7 days apart. After the demographic data of the patients are recorded with the form prepared by us, they will be evaluated with the AOFAS Midfoot Scale, Foot and Ankle Ability Measure/FAAM, SF-12 Quality of Life Scale, Visual Analogue Scale (VAS).

Sponsors & Collaborators

  • University of Beykent

    lead OTHER

Principal Investigators

  • assis.prof. Altuğ Duramaz · ISTANBUL BAKIRKOY DR. SADİ KONUK EDUCATION AND RESEARCH HOSPITAL

  • as.dr. Alican Koluman · ISTANBUL BAKIRKOY DR. SADİ KONUK EDUCATION AND RESEARCH HOSPITAL

  • as.dr. Mehmet Utku Çiftçi · ISTANBUL BAKIRKOY DR. SADİ KONUK EDUCATION AND RESEARCH HOSPITAL

  • assis.prof. Tansu Birinci · Istanbul Medeniyet University

Eligibility

Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2021-07-01
Primary Completion
2022-09-01
Completion
2022-09-27

Countries

  • Turkey (Türkiye)

Study Locations

More Related Trials

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT05246488 on ClinicalTrials.gov