Actively Recruiting

Age: 18Years +
All Genders
NCT05992064

Wearable Sensors for Monitoring Recovery After Total Knee Arthroplasty

Led by Aalborg University Hospital · Updated on 2025-04-10

30

Participants Needed

1

Research Sites

133 weeks

Total Duration

On this page

Sponsors

A

Aalborg University Hospital

Lead Sponsor

A

Aalborg University

Collaborating Sponsor

AI-Summary

What this Trial Is About

The goal of this observational study is to investigate the potential of wearable sensors for monitoring the postoperative recovery of patients after TKA. The main question the study aims to answer is: • whether alterations in gait characteristics and the changes in PA levels measured by wearable PA trackers can accurately reflect a patient's postoperative recovery status and provide clinically relevant information to aid their management. Participants will wear PA trackers during the perioperative period of TKA (2 weeks before until 3 months after, and then agin for 2 weeks one year after the surgery) and we will analyze their gait and PA and correlate them with their recovery after surgery.

CONDITIONS

Official Title

Wearable Sensors for Monitoring Recovery After Total Knee Arthroplasty

Who Can Participate

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Patients diagnosed with knee osteoarthritis scheduled for unilateral total knee arthroplasty at Aalborg University Hospital, Fars�f8.
Not Eligible

You will not qualify if you...

  • Daily pain rated 4 or higher on a numeric scale or severe osteoarthritis in the opposite knee (KL-IV).
  • Daily pain rated 4 or higher or severe osteoarthritis in the spine or other lower limb joints.
  • Body mass index over 35 kg/m2.
  • Recent surgery in spine or lower limbs within 6 months.
  • Neurological movement disorders.
  • Inflammatory arthritis.
  • Not a smartphone user.
  • Frailty score of 5 or higher on the clinical frailty scale.
  • Living in a nursing home.
  • Dependent on walking aids for movement.
  • Dementia or memory problems.
  • Skin sensitivity or issues at the plaster site.

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

Regionshospital Nordjylland, Frederikshavn

Frederikshavn, North Denmark, Denmark, 9900

Actively Recruiting

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Research Team

A

Arash Ghaffari, MD

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

0

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