ClinConnect ClinConnect Logo
Search / Trial NCT07033390

Monitor Orthopaedic Footwear Questionnaire (MOS) Validity and Reliability Study

Launched by MEDIPOL UNIVERSITY · Jun 13, 2025

Trial Information

Current as of August 23, 2025

Enrolling by invitation

Keywords

Validity Reability Orthopedic Shoes Survey

ClinConnect Summary

The translation procedure and cross-cultural adaptation of the MOS will be carried out according to the predetermined cross-cultural adaptation principles of Beaton et al. For the development of the Turkish adaptation of the MOS and the validity and reliability study, permission was obtained by e-mail from Jaap Van Netten, the first author of the original questionnaire. Firstly, two independent translators will translate the original questionnaire from English to Turkish. One of the translators will be informed about the study, the other will not be informed about the study. A draft version...

Gender

ALL

Eligibility criteria

  • Inclusion Criteria:
  • • 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

About Medipol University

Medipol University is a leading academic institution dedicated to advancing medical research and clinical innovation. With a strong emphasis on interdisciplinary collaboration, the university conducts rigorous clinical trials aimed at improving patient outcomes and enhancing healthcare practices. Leveraging state-of-the-art facilities and a team of experienced researchers and healthcare professionals, Medipol University is committed to contributing to the global medical community through ethical research and the development of novel therapeutic strategies. The institution fosters an environment of academic excellence and integrity, ensuring that all trials adhere to the highest standards of safety and efficacy.

Locations

Beykoz, Istanbul, Turkey

Patients applied

0 patients applied

Timeline

First submit

Trial launched

Trial updated

Estimated completion

Not reported