Physical Activity Levels During Recovery Following Knee Arthroplasty

Phase

N/A

Condition

N/A

Treatment

N/A

Clinical Study ID

NCT04240769

IRAS 260855

19/SW/0151

Ages > 18
All Genders

Study Summary

The goal of this study is to utilize physical activity monitoring to determine the trajectory of normal recovery as it relates to a patient's ability to get up and get moving. From this work, we hope to be able to define the range in patients' physical activity following knee replacement surgery, and thus, give clinicians a tool and the methodology to identify patients whose recovery is not progressing as quickly as expected. Data from physical activity monitors will allow the research team to identify how active patients are, how vigorous that activity is, and how well that activity correlates with standard and commonly used patient questionnaires.

Eligibility Criteria

Inclusion

Inclusion Criteria:

Participant is willing and able to give informed consent for participation in thestudy.
Male or Female, aged 18 years or above.
Diagnosed with required late stage osteoarthritis, undergoing knee arthroplasty in thenext 3 months.
In Investigator's opinion, is able and willing to comply with all trial requirements.

Exclusion

Exclusion Criteria:

Any other significant disease or disorder which, in the opinion of the Investigator,may either put the participants at risk because of participation in the study, or mayinfluence the result of the study, or the participant's ability to participate in thestudy.
Participants who are enrolled in another research study involving an investigationalproduct or methodology that could alter physical activity.
Participants are undergoing a revision arthroplasty surgery on the operative knee

Study Design

January 31, 2020

October 01, 2021

Study Description

This study is an observational study of the physical activity levels of adults who have been diagnosed with end-stage osteoarthritis of the knee and are undergoing knee replacement surgery at the Nuffield Orthopaedic Centre, Oxford. Data regarding patient activity and functional recovery will be collected using two methods. First, data will be collected through the extraction of three-axis accelerometer data, collected via a wrist-worn (and hip-worn for a subset of patients) physical activity monitor. This data will be collected in three intervals: pre-operatively, immediately postoperatively, and at 6 months postoperatively. Secondly, data will be collected by standard clinical assessment and patient reported outcome measures. These assessments will again take place pre-operatively, at 6 weeks postoperatively, and at 6 months postoperatively. Additional data will be collected through a simple activity diary, which asks the participants to log their monitor wear-time along with the times that they took bicycle rides or extended walks.

The expected duration of patient involvement is up to a total of 8 to 8.5 weeks over the course of up to 7 months. There are no clinical visits within this protocol beyond what is already within normal patient care. Patients will be asked to post their monitor back to the research centre for data collection and data processing twice during the study period.

The aim of this study is to assess the trajectory of recovery in terms of physical activity in the post-operative knee replacement population, and subsequently to define the expected path of early recovery.

Connect with a study center

Nuffield Orthopaedic Centre, Oxford University Hospitals Trust
Oxford, Oxfordshire OX3 7LD
United Kingdom
Active - Recruiting

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