Actively Recruiting

Phase Not Applicable
Age: 18Years +
All Genders
NCT07080814

The Effect of Balance Training Using a Dynamometric Platform in Patients Undergoing Total Knee Arthroplasty

Led by Ankara Etlik City Hospital · Updated on 2025-07-23

46

Participants Needed

1

Research Sites

104 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

Total knee arthroplasty (TKA) is a common surgery used to treat advanced knee osteoarthritis, especially when other treatments no longer help. While the surgery often reduces pain and improves joint alignment, many patients still have problems with balance and movement afterward. This study will explore whether adding balance training using the Tecnobody ProKin system to standard physical therapy helps patients recover better after TKA. The researchers will measure balance, walking ability, leg strength, and body awareness (also called proprioception) using special equipment. The main goal is to test the hypothesis that technology-supported balance training improves recovery outcomes more effectively than standard rehabilitation alone.

CONDITIONS

Official Title

The Effect of Balance Training Using a Dynamometric Platform in Patients Undergoing Total Knee Arthroplasty

Who Can Participate

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Patients who have undergone total knee arthroplasty within the past 2 years and are hospitalized at the Orthopedic Rehabilitation Clinic of Ankara Etlik City Hospital, Physical Therapy Hospital
  • Able to fully bear weight on the operated lower extremity in the third postoperative week
  • Willingness to participate and signing of the written informed consent form
Not Eligible

You will not qualify if you...

  • Bilateral knee arthroplasty
  • Age under 18 years
  • Receiving treatment at a physical therapy unit within the first 2 weeks after knee arthroplasty
  • Presence of significant visual or hearing impairment, active infection
  • Clinically unstable condition
  • Presence of central nervous system lesions (e.g., stroke, multiple sclerosis)
  • Presence of malignancy
  • Presence of a fracture in the lower extremity
  • Presence of any condition that would prevent participation in the treatment
  • History of lumbar disc surgery
  • History of previous surgery in the lower extremity
  • Presence of advanced osteoarthritis in the non-operated lower extremity

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

Ankara Etlik City Hospital

Ankara, Yenimahalle, Turkey (Türkiye), 06170

Actively Recruiting

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Research Team

Z

Zeynep Alpoğuz Yilmaz, MD

CONTACT

B

Başak Mansız Kaplan, Ass Prof

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

SINGLE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

TREATMENT

Number of Arms

2

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