Monitor Orthopaedic Footwear Questionnaire (MOS) Validity and Reliability Study

Brief summary (registry, in English)

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

What you commit to

• Study type: Observational
• Planned participants: 200
• From 30 Jun 2025 to the primary completion date, 30 Oct 2025
• 1 site in 1 country
• Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Who the study is looking for

Age in the registry: 16 years to 75 years · Sex: All · Accepts healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.