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

Results pending

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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Recruitment Status

COMPLETED

Clinical Phase

NA

Total Enrollment

416 participants

Study Classification

INTERVENTIONAL

Study Start Date

2021-01-18

Study Completion Date

2023-05-29

Brief Summary

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Rehabilitation after primary knee or hip arthroplasty may include performing exercises with a physiotherapist. For patients who can work well with a computer, tablet or smartphone, it is now possible to use a mobile application (e.g. moveUp) to carry out a large part of the exercises more independently. This is done with online guidance by a physiotherapist via a mobile application that is CE marked in Europe.

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).

Detailed Description

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Via the moveUP Coach App, patients receive personalized rehabilitation for knee or hip replacement, both before and after surgery. This mobile application is on the market, meets the legal requirements in Europe and has been provisionally remunerated under an agreement (convention) between the mandatory health insurance (NIHDI) and the hospital that participate in this study.

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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Arthroplasty, Replacement, Knee Rehabilitation Hip Arthrosis

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Primary Study Purpose

TREATMENT

Blinding Strategy

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.

Group Type EXPERIMENTAL

moveUp

Intervention Type DEVICE

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

Group Type EXPERIMENTAL

moveUp

Intervention Type DEVICE

Mobile application for use in the rehabilitation of primary knee and hip arthroplasty

Predefined number of traditional physiotherapy sessions

Intervention Type OTHER

exercises with a physiotherapist being physically present

Usual care

Rehabilitation after hip or knee arthroplasty without the use of a mobile application.

Group Type NO_INTERVENTION

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

Intervention Type DEVICE

Predefined number of traditional physiotherapy sessions

exercises with a physiotherapist being physically present

Intervention Type OTHER

Eligibility Criteria

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Inclusion Criteria

Eligibility 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.
Minimum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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National Institute for Health and Disability Insurance (NIHDI), Belgium

UNKNOWN

Sponsor Role collaborator

Belgium Health Care Knowledge Centre

OTHER_GOV

Sponsor Role collaborator

University Hospital, Ghent

OTHER

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

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

Site Status

Centre Hospitalier Interrégional Edith Cavell (CHIREC), site Delta

Auderghem, , Belgium

Site Status

Centre Hospitalier Interrégional Edith Cavell (CHIREC), Hôpital de Braine L'Alleud-Waterloo

Braine-l'Alleud, , Belgium

Site Status

AZ Sint-Jan Brugge

Bruges, , Belgium

Site Status

AZ Monica Deurne

Deurne, , Belgium

Site Status

AZ Alma Eeklo

Eeklo, , Belgium

Site Status

AZ Maria Middelares

Ghent, , Belgium

Site Status

Universitair Ziekenhuis Gent

Ghent, , Belgium

Site Status

Jan Yperman Ziekenhuis

Ieper, , Belgium

Site Status

CHU de Liège, site du Sart Tilman

Liège, , Belgium

Site Status

AZ Damiaan

Ostend, , Belgium

Site Status

Countries

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Belgium

Other Identifiers

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KCE HTA C2020-1

Identifier Type: -

Identifier Source: org_study_id

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