Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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RECRUITING
80 participants
OBSERVATIONAL
2023-12-27
2025-11-30
Brief Summary
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Detailed Description
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1. To evaluate change in postural stability between the DA and DL surgical approaches during the first three months after elective unilateral THA for OA, using both a clinical measure and an instrumented measure.
2. To evaluate change in balance confidence between the DA and DL surgical approaches during the first three months after elective unilateral THA for OA.
Secondary objective
3. To compare the DA and DL approaches for activity levels, function, quality of life and pain during the first three months after elective unilateral THA for OA.
Conditions
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Study Design
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COHORT
PROSPECTIVE
Study Groups
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Direct Anterior
This group will consist of people undergoing elective unilateral THA for OA using the Direct Anterior surgical approach
Total Hip Arthroplasty
Total hip arthroplasty is a common surgical procedure performed in people with advanced hip osteoarthritis
Direct Lateral
This group will consist of people undergoing elective unilateral THA for OA using the Direct Lateral surgical approach
Total Hip Arthroplasty
Total hip arthroplasty is a common surgical procedure performed in people with advanced hip osteoarthritis
Interventions
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Total Hip Arthroplasty
Total hip arthroplasty is a common surgical procedure performed in people with advanced hip osteoarthritis
Other Intervention Names
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Eligibility Criteria
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Inclusion Criteria
* Ambulatory for a minimum of 10 meters with or without a mobility aid but without the assistance of another person
* Able to read, write and speak English
* Able to provide consent
Exclusion Criteria
* Underwent THA surgery for a diagnosis other than OA
* Any condition that will prevent participants from completing the study such as having a significant neurological, cardiovascular, musculoskeletal condition as denoted by their physician.
60 Years
ALL
No
Sponsors
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Western University, Canada
OTHER
Responsible Party
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Principal Investigators
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Brent Lanting, MD
Role: PRINCIPAL_INVESTIGATOR
London Health Sciences Centre
Locations
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London Health Sciences Centre- University Hospital
London, Ontario, Canada
Countries
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Central Contacts
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Facility Contacts
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Other Identifiers
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123634
Identifier Type: -
Identifier Source: org_study_id
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