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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NOT_YET_RECRUITING
NA
20 participants
INTERVENTIONAL
2025-06-01
2025-12-01
Brief Summary
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Detailed Description
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This experimental study will involve two groups: postmenopausal women with gonarthrosis and age-matched healthy controls. Participants will undergo an isokinetic fatigue protocol followed by assessments of passive and active joint position sense being more vulnerable. Understanding these changes will contribute to developing rehabilitation strategies focusing on proprioception and fatigue management.
We expect that isokinetic fatigue will impair proprioception, with active joint position
Conditions
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Study Design
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RANDOMIZED
PARALLEL
OTHER
NONE
Study Groups
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Healthy Control
Age- and sex-matched postmenopausal women without knee pathology. Participants will perform the same passive and active joint position sense tests as the gonarthrosis group, before and after a control fatigue protocol using the Biodex system.
Fatigue Protocol + Joint Position Sense Testing
Groups will undergo an isokinetic fatigue protocol at 180°/s using a Biodex dynamometer. Passive and active joint position sense tests will be performed before and after fatigue.
Gonarthrosis Group
Postmenopausal women aged 50-65 with Kellgren-Lawrence Grade 2-3 knee osteoarthritis.
Participants will undergo an isokinetic fatigue protocol at 180°/s using a Biodex dynamometer. Passive and active joint position sense tests will be performed before and after fatigue.
Fatigue Protocol + Joint Position Sense Testing
Groups will undergo an isokinetic fatigue protocol at 180°/s using a Biodex dynamometer. Passive and active joint position sense tests will be performed before and after fatigue.
Interventions
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Fatigue Protocol + Joint Position Sense Testing
Groups will undergo an isokinetic fatigue protocol at 180°/s using a Biodex dynamometer. Passive and active joint position sense tests will be performed before and after fatigue.
Eligibility Criteria
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Inclusion Criteria
* Postmenopausal
* Grade 2-3 knee osteoarthritis (Kellgren-Lawrence Scale) for OA group
* No lower extremity surgery in the last 6 months
* No neuromuscular or orthopedic condition affecting the lower extremities
Exclusion Criteria
* Bilateral knee prosthesis or severe osteoporosis
* Lower extremity musculoskeletal injury in the last 6 months
45 Years
65 Years
FEMALE
Yes
Sponsors
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Inonu University
OTHER
Kocaeli Sağlık ve Teknoloji Üniversitesi
OTHER
Responsible Party
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Central Contacts
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Other Identifiers
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KOSTU-25-OA-01
Identifier Type: -
Identifier Source: org_study_id
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