nderstanding and predicting recovery in patients undergoing total knee replacement

Not Applicable

Completed

• Conditions: Total Knee Arthroplasty (TKA); knee replacement; Musculoskeletal - Osteoarthritis; Musculoskeletal - Other muscular and skeletal disorders

• Registration Number: ACTRN12619001000190
• Lead Sponsor: Centre for Rehab Innovations, University of Newcastle

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Study Start: 2019-07-15
• Study Completion: 2022-09-15
• Last Update Posted: 22 May 2023

Recruitment & Eligibility

• Status: Completed
• Sex: All
• Target Recruitment: 1148

Inclusion Criteria

•Ability to complete the patient reported outcome measures (questionnaires),
•Undergoing primary total knee replacement (bilateral or unilateral)

Exclusion Criteria

•Having primary total knee replacement due to trauma
•Previous knee surgery within the past 6 months
•Planned knee surgery within the next 12 months
•Not having the capacity to provide informed consent to the research.

Study & Design

• Study Type: Observational
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Goal Achievement as measured by satisfaction questionnaire and Value Living Scale[3 months post surgery];Functional mobility and pain as measured by: the Western Ontario and McMaster Universities Osteoarthritis Index (WOMAC)[Up to 4 weeks presurgery and 3 months post surgery];Quality of Life as measured on the SF-12[Up to 4 weeks pre-surgery and 3 months post surgery]

Secondary Outcome Measures

Name	Time	Method
Functional performance as measured by independent and composite measures of performance on the Timed Up and Go test, walking speed, grip strength and the 30-second chair stand test. [Up to 4 weeks pre-surgery and three months post-surgery.];Depression, anxiety, and stress as measured on the Depression, Anxiety and Stress Scale (DASS 21)[Up to 4 weeks pre-surgery and three months post-surgery.];Perceived intensity of pain as measured by the Pain Catastrophizing Questionnaire (PCS)<br>[Up to 4 weeks pre-surgery ];The capacity to recover from difficulties as measured by the brief resilience scale[Up to 4 weeks pre-surgery ]