We hypothesize that telemonitoring through SpA-Net, in combination with patient-initiated care, will lead to less outpatient visits, without compromising quality of care and health outcomes. Furthermore, we expect that telemonitoring through SpA-Net…
ID
Bron
Verkorte titel
Aandoening
- Auto-immuunziekten
Aandoening
Spondyloarthritis
Betreft onderzoek met
Ondersteuning
Onderzoeksproduct en/of interventie
- Overige
Uitkomstmaten
Primaire uitkomstmaten
At least 25% reduction in the number of scheduled and unscheduled outpatient visits to the rheumatology department in the telemonitoring group compared to the standard care group within a 1-year follow-up period.
Achtergrond van het onderzoek
Spondyloarthritis (SpA) is a chronic inflammatory rheumatic disease with a heterogeneous presentation. Regular and personalised monitoring of disease activity, physical functioning, medication use and side effects is essential to improve and maintain patients’ health-related quality of life (HRQoL) in SpA. Furthermore, care provided should be patient-centred, involving patients in treatment decisions and incorporating personal preferences, needs and values. Increasingly, transparency on outcomes of care delivered and efficiency of care are demanded. In daily practice, capacity issues, time constraints, lack of optimal tools for monitoring and providing transparency may hinder these important aspects of quality of care. Traditionally outpatient visits are pre-booked every 3-6 months, but these are frequently unnecessary in stable patients with low disease activity. Remote monitoring through a web application (telemonitoring) could be a solution for these patients. Telemonitoring has been shown to be possible, effective and safe in several chronic diseases, and clearly reduced health care utilization. To date, this has never been tested in SpA. In 2016, a web-based eHealth system for patients with SpA in the Netherlands (‘SpA-Net’) was developed as a personal monitoring system. SpA-Net includes clinical information on medication use, laboratory tests, several patient reported outcomes and a personal treatment plan, providing a comprehensive view of the patient for the rheumatologists. An excerpt of this is available to patients. This serves as the basis for each outpatient consultation. Since 2016, SpA-Net has been increasingly used in daily practice. Focus interviews among patients and care providers showed high satisfaction and acceptance of SpA-Net. It is, however, unknown whether SpA-Net can also be used as a telemonitoring system, thereby replacing face-to-face consultations, and leading to a reduction in health care utilisation. In this study, remote care (telemonitoring) provided through SpA-Net, in combination with patient-initiated care, is compared with standard care, aiming at more efficient care. Concomitantly, a trial-based cost-utility analysis will be performed.
Doel van het onderzoek
We hypothesize that telemonitoring through SpA-Net, in combination with patient-initiated care, will lead to less outpatient visits, without compromising quality of care and health outcomes. Furthermore, we expect that telemonitoring through SpA-Net could reduce healthcare expenditures and/or societal costs.
Onderzoeksopzet
Inclusion period December 2020 – July 2021 Follow up period December 2020 – July 2022 Data analysis, manuscript preparation July 2022 – January 2023 Cost-effectiveness analysis January 2023 – July 2023
Onderzoeksproduct en/of interventie
Asynchronous telemonitoring (met behulp van SpA-Net) in combinatie met patiënt-geïnitieerde zorg
Publiek
Kasper Hermans
0031433884292
kasper.hermans@mumc.nl
Wetenschappelijk
Kasper Hermans
0031433884292
kasper.hermans@mumc.nl
Leeftijd
Belangrijkste voorwaarden om deel te mogen nemen (Inclusiecriteria)
In order to be eligible for participation in this study, subjects must meet all of the following criteria: • Adult patient (18+ years) • Diagnosis of SpA according to treating physician • At least 2 years of disease duration, to be familiar with signs, symptoms, and medication • Stable disease, defined as being in a patient acceptable symptom state according to patient AND treating physician (36) AND no treatment change expected in the next few months • Access to a computer, tablet and/or smartphone for the entire duration of the study
Belangrijkste redenen om niet deel te kunnen nemen (Exclusiecriteria)
A potential subject who meets any of the following criteria will be excluded from participation in this study: • Insufficient mastery of Dutch language • Incompetent to act for oneself • Limited life expectancy • Ongoing (or planned) pregnancy during the study period • Patients participating in other research project(s)
Opzet
Deelname
Voornemen beschikbaar stellen Individuele Patiënten Data (IPD)
Postbus 5800
6202 AZ Maastricht
043 387 6009
secretariaat.metc@mumc.nl
Opgevolgd door onderstaande (mogelijk meer actuele) registratie
Andere (mogelijk minder actuele) registraties in dit register
Geen registraties gevonden.
In overige registers
Register | ID |
---|---|
NTR-new | NL7883 |
CCMO | NL71041.068.19 |
ClinicalTrials.gov | NCT04673825 |
OMON | NL-OMON54628 |