Patient Reported Outcome Measures (PROMs) in Rehabilitation With or Without the Possible Use of a Mobile Application After Primary Knee or Hip Arthroplasty
NCT ID: NCT04628468
Last Updated: 2023-07-07
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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COMPLETED
NA
416 participants
INTERVENTIONAL
2021-01-18
2023-05-29
Brief Summary
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This study will investigate whether the effect of the mobile application on knee or hip rehabilitation and quality of life is equal to that of standard care (i.e. without the use of a mobile application).
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Detailed Description
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Eligible patients will be randomized to one of the three treatment options of the study:
1. The "usual care group" will not be informed in detail about the mobile application and will receive usual rehabilitation care for knee- or hip replacement.
2. The group "possibility to use the mobile application with a predefined number of physiotherapy sessions" will receive all necessary information on the mobile application and can still decide whether or not to receive rehabilitation with online guidance by a physiotherapist via the mobile application. A predefined number of traditional physiotherapy sessions is combined with the use of the mobile app in this group.
3. The group "possibility to use the mobile application without a predetermined number of physiotherapy sessions" will receive all necessary information on the mobile application and can still decide whether or not to receive rehabilitation with online guidance by a physiotherapist via the mobile application. No predefined number of traditional physiotherapy sessions are required.
The patient will be asked to complete 2 questionnaires (KOOS-JR/HOOS-JR and EQ5D-5L) at baseline, 6 weeks and 6 months after arthroplasty. These patient reported outcomes will give an indication on the rehabilitation outcome and quality of life compared in the 3 groups.
At the end of the study, a health economic evaluation is foreseen by the Federal Knowledge Center for Healthcare (KCE). In this way the results can be helpful in getting a more definitive refund for the mobile application in Belgium.
Conditions
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Study Design
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RANDOMIZED
PARALLEL
TREATMENT
NONE
Study Groups
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Possibility to use the mobile application without a predefined number of physiotherapy sessions
Rehabilitation after hip or knee arthroplasty with the option to use a mobile application and no predefined traditional physiotherapy.
moveUp
Mobile application for use in the rehabilitation of primary knee and hip arthroplasty
Possibility to use the mobile application with a predefined number of physiotherapy sessions
Rehabilitation after hip or knee arthroplasty with the option to use a mobile application and a predefined number of traditional physiotherapy sessions
moveUp
Mobile application for use in the rehabilitation of primary knee and hip arthroplasty
Predefined number of traditional physiotherapy sessions
exercises with a physiotherapist being physically present
Usual care
Rehabilitation after hip or knee arthroplasty without the use of a mobile application.
No interventions assigned to this group
Interventions
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moveUp
Mobile application for use in the rehabilitation of primary knee and hip arthroplasty
Predefined number of traditional physiotherapy sessions
exercises with a physiotherapist being physically present
Eligibility Criteria
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Inclusion Criteria
1. The patient is aged 18 years or older, has a Belgian National Number, is insured by a Belgian sickness fund, and is not staying in a nursing home or long term rehabilitation centre.
2. The patient has sufficient knowledge of Dutch, French, German or English.
3. The patient has a planned date between the next 1 to 8 weeks for a primary unilateral unicompartmental knee arthroplasty (UKA); a bicompartmental knee arthroplasty, (BKA), consisting of either two UKA or a UKA and a patellar replacement; or a total knee arthroplasty (TKA) or a total hip arthroplasty (THA).
4. The patient is not planned to have a peri-operative procedure (e.g. intra-articular catheter) or postoperative procedure that is expected to significantly impact the rehabilitation in and out of hospital.
5. In the 6 months after arthroplasty the patient is not planned to have surgery that may impact the arthroplasty rehabilitation.
6. The patient is not suffering from a medical condition (e.g. Parkinson, multiple sclerosis, cerebrovascular accident) that is expected to significantly impact the rehabilitation or that constitutes a contra-indication for the use of the mobile application.
7. The patient confirms to have easy and daily access to the internet, a mobile phone, a personal email address and a computer, tablet or smartphone, until 8 months after randomization.
8. The patient does not upfront exclude the possibility whereby part of the rehabilitation is performed without a physical therapist physically being present.
9. The patient is willing to complete online the patient reported outcomes and is aware that if he/she fails in this computer literacy test (performed before randomization) he/she will not be randomized and hence not included in the study. He/she will receive usual rehabilitation care.
18 Years
ALL
No
Sponsors
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National Institute for Health and Disability Insurance (NIHDI), Belgium
UNKNOWN
Belgium Health Care Knowledge Centre
OTHER_GOV
University Hospital, Ghent
OTHER
Responsible Party
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Principal Investigators
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Catherine Van Der Straeten, Professor
Role: STUDY_DIRECTOR
Health, Innovation and Research Institute UZ Ghent
Locations
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Antwerp University Hospital
Antwerp, , Belgium
Centre Hospitalier Interrégional Edith Cavell (CHIREC), site Delta
Auderghem, , Belgium
Centre Hospitalier Interrégional Edith Cavell (CHIREC), Hôpital de Braine L'Alleud-Waterloo
Braine-l'Alleud, , Belgium
AZ Sint-Jan Brugge
Bruges, , Belgium
AZ Monica Deurne
Deurne, , Belgium
AZ Alma Eeklo
Eeklo, , Belgium
AZ Maria Middelares
Ghent, , Belgium
Universitair Ziekenhuis Gent
Ghent, , Belgium
Jan Yperman Ziekenhuis
Ieper, , Belgium
CHU de Liège, site du Sart Tilman
Liège, , Belgium
AZ Damiaan
Ostend, , Belgium
Countries
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Other Identifiers
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KCE HTA C2020-1
Identifier Type: -
Identifier Source: org_study_id
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