Pilot (Feasibility) Study of Personalised Internet-based Rehabilitation Program Incorporating Electronic Functional Monitoring after Total Knee Arthroplasty

Not Applicable

Recruiting

• Conditions: total knee arthroscopy recovery; Musculoskeletal - Osteoarthritis; Physical Medicine / Rehabilitation - Other physical medicine / rehabilitation; Surgery - Other surgery

• Registration Number: ACTRN12616001589471
• Lead Sponsor: Trifecta Pty Ltd

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Study Start: 2016-11-17
• Last Update Posted: 13 January 2020

Recruitment & Eligibility

• Status: Recruiting
• Sex: All
• Target Recruitment: 50

Inclusion Criteria

Age >18 years
1. Patients considered suitable for a total knee arthroplasty by their treating surgeon
2. Patients willing to give written informed consent and to participate and comply with the requirements of the study.
3. Willing and able to use a Smart device (e.g. a tablet)
4. Has internet access

Exclusion Criteria

1. Patients who are not willing to engage with an internet-based functional monitoring and treatment program.
2. Patients unwilling to complete a series of validated psychological and functional self-report questionnaires

Study & Design

• Study Type: Interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
The primary outcome is success, in terms of patient satisfaction with the protocol, as assessed by a daily question:<br>Are you satisfied with the program? The response is YES or NO.<br><br><br>[Daily from the baseline visit (device fitting) through to device removal (6 weeks or 12 weeks)]