Monitor Orthopaedic Footwear Questionnaire (MOS) Validity and Reliability Study

NCT07033390 | Enrolling By Invitation DMC

• 1 other identifier: İsciH
• Study Type: observational
• Target: 200
• Locations: 1 country
• Sites: 1

Brief 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

Keywords

validity; reability; orthopedic shoes; survey

Outcome Measures

Primary Outcomes (2)

• validity

  RMSEA and CFI values in confirmatory factor analysis

  2-month change

• reliability

  Cronbach's alpha and ICC value

  2-month change

Interventions

survey OTHER

validity and reliability study of MOS

Eligibility Criteria

• Age: 16 Years - 75 Years
• Sex: all
• Healthy Volunteers: Yes
• Age Groups: Child (0-17), Adult (18-64), Older Adult (65+)
• Sampling Method: Probability Sample

Study Population

Individuals using insoles

You may qualify if:

• Wearing orthopedic shoes for the first time,
• Being 16 years old and above,
• Being a native Turkish speaker and having at least a literacy level,
• Being able to complete the survey without assistance regarding cognitive or physical disorders,
• Volunteering to participate in the study

Sponsors & Collaborators

• Medipol University: lead

Study Sites (1)

Istanbul Medipol University

Beykoz, Istanbul, 34290, Turkey (Türkiye)

Location

MeSH Terms

Interventions

Surveys and Questionnaires

Intervention Hierarchy (Ancestors)

Data Collection; Epidemiologic Methods; Investigative Techniques; Health Care Evaluation Mechanisms; Quality of Health Care; Health Care Quality, Access, and Evaluation; Public Health; Environment and Public Health

Study Design

• Study Type: observational
• Observational Model: OTHER
• Time Perspective: CROSS SECTIONAL
• Sponsor Type: OTHER
• Responsible Party: PRINCIPAL INVESTIGATOR
• PI Title: Lecturer

Study Record Dates

• First Submitted: June 13, 2025
• First Posted: June 24, 2025
• Study Start: June 30, 2025
• Primary Completion: October 30, 2025
• Study Completion: November 30, 2025
• Last Updated: June 24, 2025

Record last verified: 2025-06

Locations

TU (1)