Actively Recruiting

Age: 40Years - 90Years
All Genders
NCT06821269

Functional Recovery After Total Knee Arthroplasty

Led by University of Pittsburgh · Updated on 2025-12-11

30

Participants Needed

1

Research Sites

191 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

The goal of this observational study is to learn about patients' recoveries after receiving total knee arthroplasty (TKA). The main questions it aims to answer are: Does robotic-assisted TKA have improved perceived recovery when compared to conventional TKA? Does robotic-assisted TKA lead to improved functional recovery when compared to conventional TKA? Researchers will compare if robotic-assisted versus conventional procedures lead to different recovery speeds. Participants will answer questionnaires and undergo physical therapy testing before and at several timepoints after their procedure.

CONDITIONS

Official Title

Functional Recovery After Total Knee Arthroplasty

Who Can Participate

Age: 40Years - 90Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Candidate for total knee arthroplasty (TKA)
  • Ability to speak English and understand study instructions
  • Medical clearance from primary care provider, principal investigator, or co-investigator
  • Willingness to comply with all study procedures and availability for the entire study duration
Not Eligible

You will not qualify if you...

  • History of two or more falls in the past year
  • Unable to walk 100 feet without an assistive device or rest
  • Presence of acute illness
  • History of cardiovascular disease or uncontrolled hypertension
  • Severe visual impairment
  • Lower-extremity amputation
  • Neurological, muscular, systemic, or connective tissue disorder affecting lower extremity function
  • Pregnant
  • Terminal illness
  • Plans to have another joint replacement during the study
  • Plans to relocate away from the study area during the study period

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

University of Pittsburgh

Pittsburgh, Pennsylvania, United States, 15213

Actively Recruiting

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Research Team

V

Victoria Wong, BA

CONTACT

How is the study designed?

Study Type

OBSERVATIONAL

Masking

N/A

Allocation

N/A

Model

N/A

Primary Purpose

N/A

Number of Arms

4

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