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Chronıc Ankle Instabılıty And Assocıated Factors

NCT04064502 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 273

Last updated 2019-08-22

No results posted yet for this study

Summary

The purpose of this study was to evaluate the prevalence of chronic ankle instability using the Cumberland Ankle Instability Tool (CAIT) and investigate the independent associated factors. The data was collected from adult volunteers by questionnaire including sociodemographic information, general medical condition, history of orthopedic surgery, pain intensity, and the number of painful areas of the foot.

Conditions

  • Chronic Ankle Instability

Interventions

DIAGNOSTIC_TEST

CHRONIC ANKLE INSTABILITY AND ASSOCIATED FACTORS:

Questionnaire including sociodemographic information, general medical condition, history of orthopedic surgery, pain intensity, and the number of painful areas of the foot.

Sponsors & Collaborators

  • Yeditepe University Hospital

    collaborator OTHER

  • Yeditepe University

    lead OTHER

Principal Investigators

  • Uğur Şaylı, MD, Prof. · Yeditepe University Hospital

  • Şule Demirbaş, Asst.Prof. · editepe University, Faculty of Health Sciences, Deparment of Physiotherapy and Rehabilitation

  • Feryal Subaşı, PT, Prof. · Yeditepe University, Faculty of Health Sciences, Deparment of Physiotherapy and Rehabilitation

  • Ebru Akbuğa, MSc, PT · Yeditepe University, Faculty of Health Sciences, Deparment of Physiotherapy and Rehabilitation

  • Elif Tuğçe Çil, MSc, PT · Yeditepe University, Faculty of Health Sciences, Deparment of Physiotherapy and Rehabilitation

Eligibility

Min Age
18 Years
Max Age
34 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2017-05-01
Primary Completion
2017-12-01
Completion
2018-09-01

Countries

  • Turkey (Türkiye)

Study Locations

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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 NCT04064502 on ClinicalTrials.gov