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Clinical Trial Summary

This trial is a randomized feasibility trial to determine the feasibility of comparing two different shoe inserts and on pain, quality of life and physical activity associated with hip osteoarthritis.


Clinical Trial Description

Participants will be randomized to one of two groups - contoured prefabricated foot orthoses or flat shoe inserts (the comparator). Participants will be asked to use the inserts daily for a six week period. Adherence to the intervention will be monitored using a daily diary, as well as adverse events and co-interventions. The primary outcome is feasibility domains (Demand, Implementation, Acceptability, Practicality) with secondary outcomes of change in hip-related pain and quality of life and physical activity levels. The primary time-point will be 6-weeks. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT05138380
Study type Interventional
Source La Trobe University
Contact Adam Semciw, PhD
Phone +61394796452
Email a.semciw@latrobe.edu.au
Status Recruiting
Phase N/A
Start date February 1, 2022
Completion date October 26, 2025

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