Shoe Orthotics for Improvement of Biomechanics and Symptoms of Knee Osteoarthritis

NACompletedINTERVENTIONAL
Enrollment

26

Participants

Timeline

Start Date

August 31, 2014

Primary Completion Date

March 31, 2016

Study Completion Date

March 31, 2016

Conditions
Knee Osteoarthritis
Interventions
DEVICE

Lateral wedge

This will be a randomized cross-over study where all participants will receive both orthoses over a six month period. Each intervention will last two months, separated by a two month washout period of no orthotics wear, and will be preceded and followed by a laboratory-based gait and pain assessment. Two months has been chosen as the ideal time frame to ensure maximum participant adherence, to observe clinically meaningful changes in symptoms, and to minimize degradation of the insoles.

DEVICE

Lateral wedge plus medial arch support

This will be a randomized cross-over study where all participants will receive both orthoses over a six month period. Each intervention will last two months, separated by a two month washout period of no orthotics wear, and will be preceded and followed by a laboratory-based gait and pain assessment. Two months has been chosen as the ideal time frame to ensure maximum participant adherence, to observe clinically meaningful changes in symptoms, and to minimize degradation of the insoles.

Trial Locations (1)

Unknown

University of British Columbia; University Hospital, Vancouver

All Listed Sponsors
collaborator

Pedorthic Research Foundation of Canada

UNKNOWN

collaborator

Kintec Footlabs

UNKNOWN

lead

University of British Columbia

OTHER

NCT02234895 - Shoe Orthotics for Improvement of Biomechanics and Symptoms of Knee Osteoarthritis | Biotech Hunter | Biotech Hunter