- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05294224
The Relationship Between Disease Severity and Various Lower Extremity Parameters in Individuals With Knee Osteoarthritis
Study Overview
Status
Conditions
Detailed Description
Osteoarthritis (OA) is one of the most common chronic degenerative diseases in the world, which progresses slowly, can cause pain, stiffness and dysfunction, and reduces the quality of life.
OA is particularly common in weight-bearing joints such as the knee and the functional status of patients with OA is adversely affected various factors such as immobility due to pain, decrease in muscle strength and joint range of motion, etc.
In relation to this, walking difficulty and decrease in walking speed, balance problems and an increase in the risk of falling are a picture that can be encountered in the later stages of the disease.
The aim of this study is to investigate the relationship between QF strength, QF thickness, femoral cartilage thickness, knee function, balance, kinesiophobia and gait of the patients with knee OA.
Study Type
Enrollment (Actual)
Contacts and Locations
Study Contact
- Name: Dilara Özen Oruk
- Phone Number: 05542039899
- Email: fztdilaraozen@gmail.com
Study Locations
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Muğla, Turkey, 48000
- Muğla Sıtkı Koçman University
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Sampling Method
Study Population
Description
Inclusion Criteria:
- Volunteer patients who applied to the Physical therapy and Rehabilitation department with knee pain
Exclusion Criteria:
- Individuals who have received intra-articular therapy for gonarthrosis in the last 6 months, who have undergone arthroscopic surgery, and who have additional pathologies in their lower extremities
- Individuals with physical, mental and/or psychological disorders that may affect participation in the study
Study Plan
How is the study designed?
Design Details
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
QF muscle thickness
Time Frame: Day 1
|
QF muscle thickness
|
Day 1
|
QF muscle strength
Time Frame: Day 1
|
QF muscle strength
|
Day 1
|
Femoral cartilage thickness
Time Frame: Day 1
|
Femoral cartilage thickness
|
Day 1
|
Knee function
Time Frame: Day 1
|
Knee function assessment with The Knee injury and Osteoarthritis Outcome Score (KOOS).
It is a 42-item questionnaire, including 5 subscales: symptoms, pain, ADLs, sports/recreation, and quality of life.
The maximum score a patient can achieve is 100, indicating no knee problems.
The minimum score is zero, indicating severe knee problems.
|
Day 1
|
Kellgreen-Lawrence Radiological Stages
Time Frame: Day 1
|
Kellgreen-Lawrence Radiological Stages: Grade 1 (doubtful): doubtful joint space narrowing and possible osteophytic lipping. grade 2 (minimal): definite osteophytes and possible joint space narrowing. grade 3 (moderate): moderate multiple osteophytes, definite narrowing of joint space and some sclerosis and possible deformity of bone ends. |
Day 1
|
Kinesiophobia
Time Frame: Day 1
|
Tampa Kinesiophobia Scale: The total score of the scale range from 17- 68, where 17 means no kinesiophobia, 68 means severe kinesiophobia, and score ± 37 indicates there is kinesiophobia.
|
Day 1
|
Balance and gait
Time Frame: Day 1
|
Tinetti Score: It uses a 3-point ordinal scale of 0, 1 and 2. Gait is scored over 12 and balance is scored over 16 totalling 28.
The lower the score on the Tinetti test, the higher the risk of falling.
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Day 1
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Low Extremity Functionality and Fall Risk
Time Frame: Day 1
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30 sec sit to stand test
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Day 1
|
Collaborators and Investigators
Sponsor
Collaborators
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- 210077/10
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
Clinical Trials on Knee Osteoarthritis
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University Hospital, Clermont-FerrandSanofiCompletedKnee Osteoarthritis (Knee OA)France
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Joseph E. BroylesCompletedDegenerative Lesion of Articular Cartilage of Knee | Degeneration; Articular Cartilage, Knee | Unilateral Primary Osteoarthritis of Knee | Osteoarthritis Knee
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The Hong Kong Polytechnic UniversityCompleted
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Jiangsu XinChen-Techfields Pharma Co., LTD.Completed
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Tianjin XinChen-Techfields Pharma Co., LTD.Completed
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Eun Jung KimMinistry of Health & Welfare, Korea; Semyung UniversityUnknownOsteoarthritis KneeKorea, Republic of
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Thammasat UniversityCompletedPrimary Knee OsteoarthritisThailand
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Galderma R&DCompletedUnilateral Knee OsteoarthritisUnited Kingdom