- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT07480473
PROPRIOCEPTION, KINESIOPHOBIA AND FUNCTIONAL RECOVERY AFTER GONARTHROSIS SURGERY
September 2, 2026 updated by: Hulya YAMAN, Medipol University
Associations of Proprioception, Kinesiophobia, Balance, and Sensory Processing Patterns With Functional Status After Total Knee Arthroplasty for Osteoarthritis
This observational study aims to investigate the relationships between proprioception, causes of kinesiophobia, sensory processing characteristics, and functional recovery in individuals undergoing gonarthrosis surgery.
Postoperative functional recovery can be influenced by sensorimotor and psychological factors such as impaired proprioception, fear of movement, and changes in sensory processing.
However, the interaction between these factors has not been sufficiently clarified.
Participants will complete a sociodemographic and clinical information form, the Western Ontario and McMaster University Osteoarthritis Index (WOMAC), the Causes of Kinesiophobia Scale, and the Adolescent/Adult Sensory Profile.
Proprioception will be assessed using the Joint Position Perception Test.
Study Overview
Status
Completed
Conditions
Study Type
Observational
Enrollment (Actual)
47
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
-
-
BEYKOZ
-
Istanbul, BEYKOZ, Turkey (Türkiye)
- Istanbul Medipol University
-
-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
- Adult
- Older Adult
Accepts Healthy Volunteers
No
Sampling Method
Non-Probability Sample
Study Population
The study population will consist of individuals who have undergone surgery for gonarthrosis and are admitted for follow-up evaluation at an orthopedic clinic.
Participants who meet the inclusion criteria and provide informed consent will be included.
The study will evaluate the relationship between proprioception, causes of kinesiophobia, sensory processing characteristics, and functional recovery in this population.
Description
Inclusion Criteria
- Individuals aged 60 years or older.
- Individuals who had undergone total knee arthroplasty (TKA) in at least one knee.
- At least two months had elapsed since the TKA procedure of the knee evaluated in the study.
- Sufficient mobility to safely complete the study assessments.
- Ability to understand and follow verbal instructions provided by the researcher.
Exclusion Criteria
- Acute or uncontrolled neurological, cardiopulmonary, or musculoskeletal conditions that could prevent the safe and appropriate completion of the study assessments.
- Acute pain or any other health problem at the time of assessment that prevented completion of the study procedures.
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Womac
Time Frame: 04.04.2026-05.05.2026
|
Womac is a widely used, self-administered questionnaire designed to evaluate pain, stiffness, and physical function in patients with knee or hip osteoarthritis.
It consists of 24 items (5 for pain, 2 for stiffness, 17 for physical function).
Higher scores indicate worse symptoms and greater functional limitations.
|
04.04.2026-05.05.2026
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Berg Balance Scale
Time Frame: 04.04.2026-05.05.2026
|
The Berg Balance Scale is a 14-item, 0-56 point scored, highly valid, objective performance test used to measure static and dynamic balance and assess fall risk.
It includes daily living movements such as getting up from a chair, standing, standing on one leg, and turning over.
|
04.04.2026-05.05.2026
|
|
Proprioception Assessment
Time Frame: 04.04.2026-05.05.2026
|
Proprioception (deep sense) assessment measures the body's ability to perceive its position in space, its movement, and joint angles.
|
04.04.2026-05.05.2026
|
|
The Causes of Kinesiophobia Scale
Time Frame: 04.04.2026-05.05.2026
|
This is a validated and reliable tool in Turkish that helps identify the biological and psychological causes underlying fear of movement.
It evaluates pain, fear of re-injury, and functional limitations in terms of their biological and psychological sub-dimensions.
It is used in cases of chronic pain and avoidance of movement.
|
04.04.2026-05.05.2026
|
|
The Adolescent Sensory Profile
Time Frame: 04.04.2026-05.05.2026
|
The Adolescent Sensory Profile is a scientific assessment tool that measures individuals' responses to sensory stimuli (sound, light, texture, movement, smell) in daily life.
By identifying sensory processing patterns, it analyzes how sensitive a person is to environmental inputs or how they seek out these inputs.
|
04.04.2026-05.05.2026
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (Actual)
April 4, 2026
Primary Completion (Actual)
May 5, 2026
Study Completion (Actual)
May 5, 2026
Study Registration Dates
First Submitted
March 14, 2026
First Submitted That Met QC Criteria
March 14, 2026
First Posted (Actual)
March 18, 2026
Study Record Updates
Last Update Posted (Actual)
September 8, 2026
Last Update Submitted That Met QC Criteria
September 2, 2026
Last Verified
March 1, 2026
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- E-10840098-202.3.02-8563
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
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.