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Knee surgery recovery: It's not just about the joint

NCT ID NCT07480473

What the study statuses mean

This study's is highlighted.

Recruitment status, easiest to join first

Recruiting now
This trial is taking on new participants right now.
Not yet recruiting
Registered, but not yet taking participants.
By invitation only
Not open to general applications. Only people the study team invites can take part.
Paused
Paused for now. It may or may not start again.
Ongoing
Running, but no longer taking on new participants.
Completed This study
The trial has finished. Results may not be published yet.
Stopped early
Stopped early, before it reached the end. That can be for many reasons, including safety.
Cancelled
Cancelled before anyone took part.

Expanded access (not trials)

Expanded access
Not a trial. This treatment can be requested outside a study, case by case, for people who qualify.
Expanded access (paused)
Not a trial. The treatment can normally be requested outside a study, but is unavailable right now.
Expanded access (ended)
Not a trial. The treatment could once be requested outside a study, but no longer can.
Approved
The treatment has been approved, so it is available normally rather than through this programme.

When the status isn't known

Details not published
The full record has not been published yet, so there is little to show here.
Status unknown
This status has not been confirmed recently, so it may be out of date.

First seen Jun 27, 2026 · Last updated Sep 09, 2026 · Updated 2 times

Summary

This study looks at how your sense of joint position, fear of moving, balance, and sensory processing affect recovery after knee osteoarthritis surgery. Researchers will measure these factors in 75 people aged 50-75 who had a total knee replacement 4-6 weeks ago. The goal is to better understand what influences functional recovery, which could help improve future rehabilitation programs.

This is an AI summary of the original study and may miss details. Read our disclaimer.

Study facts

What this study's own registry entry says, in plain language.

Participants

47 people

The number who actually took part.

Started

Apr 2026

Finished

May 2026

Lead sponsor

Other sponsor

The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.

Who can take part

This study's own entry requirements. Only the study team can say for certain whether you qualify.

Who is studied

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.

Ages

60 to 85 years

Sex

Anyone

Healthy volunteers

Not accepted

This study is not open to healthy volunteers. The entry requirements below say who it is open to.

Show the full entry requirements

Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.

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.

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Conditions

The condition(s) this trial relates to.

As listed by the trial registrant

The condition terms exactly as the trial's registrant entered them.

Contacts and locations

Locations

  • Istanbul Medipol University

    Istanbul, BEYKOZ, Turkey (Türkiye)

More trials for these conditions

Other studies related to the condition(s) this trial covers.