Patient Recovery After Knee Replacement Surgery

A Feasibility Study to Monitor Post Discharge Activity of Patient Recovery After Knee Replacement Surgery

NCT03518866•Bev Hoddell

Summary

This main objective of this feasibility study is to begin to quantify the relationship between patient activity levels following knee replacement surgery and outcomes.

Detailed Description

This main objective of this feasibility study is to begin to quantify the relationship between patient activity levels following knee replacement surgery and outcomes. Primary Aims The primary objective of this study is to compare step count and activity levels with key outcome measures - including pain scores and painkiller usage - to determine whether more active people have better recovery.

Eligibility

Age

18 - No limit years

Sex

ALL

Healthy Volunteers

Inclusion Criteria

•\* Adult
•Must be able to converse and understand English
•The participants must be selected for for single full knee replacement surgery at Milton Keynes University Hospital
•The participant must have access to a computer at home or be willing to plug a synchronization box into their broadband router
•The participants must have access to a valid email address or be able to create one for the purpose of this study (this may belong to a spouse, partner, friend or relative) or have access to a mobile phone able to receive SMS (text) messages

Exclusion Criteria

•Insufficient language skills to understand the study procedures
•Cognitive impairment
•Medical conditions (e.g., severe neurological disorder, acute cancer, psychiatric disorder, acute infections) that prevent participation in the study
•Wheelchair user
•Significant lower limb arthritic joints
•Severe mobility limitation due to central or peripheral respiratory dysfunction
•Severe mobility limitation due to central or peripheral nervous system disorders
•Severe mobility limitation due to spinal condition
•Severe mobility limitation due to musculoskeletal disabilities
•Rheumatoid arthritis due to joint pain in both upper and lower limbs
+2 more criteria

Locations (1)

Milton Keynes University Hospital NHS Foundation Trust

Milton Keynes, Bucks, United Kingdom

Key Dates

Start Date

July 21, 2015

Primary Completion Date

December 31, 2017

Completion Date

December 31, 2018

Last Updated

May 8, 2018

Enrollment

ACTUAL participants

Conditions

Total Knee Replacement

Mako Cementless TKA vs Mako Cemented TKA

NCT06929871

Total Knee ReplacementTotal Knee Replacement Surgery+2 more

View study

RECRUITINGNA

Cold and Compression Post TKA

NCT07023185

Primary Osteoarthritis Patients Scheduled for Total Knee Replacement Surgery

View study

RECRUITING

Data Source & Attribution

This clinical trial information is sourced from ClinicalTrials.gov, a service of the U.S. National Institutes of Health.

ClinicalTrials.gov last update: May 8, 2018Data synced to Clareo: March 29, 2026

Modifications: This data has been reformatted for display purposes. Eligibility criteria have been parsed into inclusion/exclusion sections. Location data has been geocoded to enable distance-based search. For the authoritative and most current information, please visit ClinicalTrials.gov.

Neither the United States Government nor Clareo Health make any warranties regarding the data. Check ClinicalTrials.gov frequently for updates.

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Patient Recovery After Knee Replacement Surgery

Inclusion Criteria

Exclusion Criteria

Mako Cementless TKA vs Mako Cemented TKA

Cold and Compression Post TKA

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