Increasing medication adherence in rheumatoid arthritis (RA) might reduce disease activity and the need to prescribe more expensive (biological) anti-rheumatic drugs. The usage of drug monitoring devices (like Medication Event Monitoring System (…
ID
Bron
Aandoening
Adherence,
Electronic Monitoring,
Rheumatoid Arthritis,
Disease activity
Therapietrouw
Reumatoïde arthritis
ziekteactiviteit
Ondersteuning
Hengstdal 3
6101 HB Nijmegen
the Netherlands
B Benraad, Director Department of Pharmacy Sint Maartenskliniek
Onderzoeksproduct en/of interventie
Uitkomstmaten
Primaire uitkomstmaten
The difference in proportion of non-adherence patients (less than 80% medication adherence) after 1 year
Doel van het onderzoek
Increasing medication adherence in rheumatoid arthritis (RA) might reduce disease activity and the need to prescribe more expensive (biological) anti-rheumatic drugs. The usage of drug monitoring devices (like Medication Event Monitoring System (MEMS™)) combined with personal feedback regarding medication behavior has proven in other diseases like HIV to be an effective strategy to improve adherence and therefore clinical outcome, decrease drug changes and drug use.Although these studies suggest that electronic drug monitor feedback might have the potential to prevent unnecessary treatment escalation in rheumatoid arthritis patients with poor adherence, empirical evidence to prove this drug-/cost saving potential is lacking. Therefore, we aim to determine if the implementation of electronic drug monitoring adherence feedback in standard care for patients with rheumatoid arthritis starting with conventional anti-rheumatic drugs is effective on medication adherence compared to a usual care group.
Onderzoeksopzet
Primary and secondary outcomes: T=0 en T=12 months
Sec outcomes: T=0, T=2 months, T=6 months, T=6 months, T=12 months
Onderzoeksproduct en/of interventie
Patients in the intervention group receive their medication during 1 year in an electronic device. Before each regular (3-monthly) consult to the rheumatologist, patient's medication adherence will be assessed by reading out the electronic device and (if necessary) possible barriers to medication intake will be discussed with the pharmacist on a semi-structured way. Patients in the control group will receive standard care (an interview with the pharmacy consultant without electronic drug monitor feedback).
Publiek
Hengstdal 3 <br>
A. Houterman
Nijmegen 6101 HB
The Netherlands
024 327 2767
a.houterman@maartenskliniek.nl
Wetenschappelijk
Hengstdal 3 <br>
A. Houterman
Nijmegen 6101 HB
The Netherlands
024 327 2767
a.houterman@maartenskliniek.nl
Belangrijkste voorwaarden om deel te mogen nemen (Inclusiecriteria)
• newly diagnosed with RA (2010 ARA criteria or clinical judgement rheumatologist)
• initiating DMARDS
• >18 years
• sufficient ability to understand Dutch
• be able to be followed for 12 months (life expectancy)
Belangrijkste redenen om niet deel te kunnen nemen (Exclusiecriteria)
• large cognitive limitations
• assistance in taking drugs (e.g. home care)
• included in another randomised controlled trial
Opzet
Deelname
Opgevolgd door onderstaande (mogelijk meer actuele) registratie
Geen registraties gevonden.
Andere (mogelijk minder actuele) registraties in dit register
Geen registraties gevonden.
In overige registers
Register | ID |
---|---|
NTR-new | NL4532 |
NTR-old | NTR4667 |
Ander register | METC : 2014/137 |