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Monitor Orthopaedic Footwear Questionnaire (MOS) Validity and Reliability Study

NCT07033390 · Status: ENROLLING_BY_INVITATION · Type: OBSERVATIONAL · Enrollment: 200

Last updated 2025-06-24

No results posted yet for this study

Summary

The aim of the study is to adapt the MOS questionnaire into Turkish and to investigate the validity and reliability of the questionnaire. In this study, Monitor Orthopaedic Shoes Questionnaire (MOS) will be translated into Turkish and named as MOS-T.

The research is a methodological study conducted to determine the validity and reliability of the Turkish adaptation of the MOS. For this purpose, the questionnaire will be translated into Turkish, cultural adaptation of the Turkish version will be made, and its validity and reliability will be tested.In accordance with the validity and reliability research, MOS will be reapplied to the participants after 8 weeks to evaluate the test-retest reliability.

Inclusion Criteria

* Wearing orthopaedic shoes for the first time,
* 16 years of age or older,
* Native language is Turkish and at least literacy level,
* Able to complete the questionnaire without assistance with cognitive or physical impairments,
* Who volunteered to participate in the study

Conditions

  • Validity and Safety

Interventions

OTHER

survey

validity and reliability study of MOS

Sponsors & Collaborators

  • Medipol University

    lead OTHER

Eligibility

Min Age
16 Years
Max Age
75 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2025-06-30
Primary Completion
2025-10-30
Completion
2025-11-30

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 NCT07033390 on ClinicalTrials.gov