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Digital Cohort of Rheumatic Disease

Adherence to self-monitoring in rheumatic disease: a prospective cohort study

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
NL-OMON
Registry ID
NL-OMON21144
Enrollment
186
Registered
2020-02-28
Start date
2020-02-28
Completion date
Unknown
Last updated
2024-02-28

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Ankylosing Spondylithis, Psoriatic Arthritis, Rheumatoid Arthritis

Interventions

At inclusion patients are asked to use the MijnReuma Reade smartphone application. The app provides the possibility to complete a weekly questionnaire. This questionnaire has been derived from the MDH

Sponsors

Pfizer, Sanofi-aventis, Novartis, Eli Lilly
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1. Patients with Ankylosing Spondylithis/Psoriatic Arthritis/ Rheumatoid Arthritis 2. Able to speak and write Dutch 3. Owning a Andriod or IOs smartphone

Exclusion criteria

Exclusion criteria: Taking part in an other digital self-monitoring trial

Design outcomes

Primary

MeasureTime frame
Adherence at 3 months

Secondary

MeasureTime frame
Adherence at 6 months, patient empowerment as measured by the Effective Consumer scale (EC-17), patient-physician interaction as measured by the Perceived Efficacy in Patient-Physician Interaction Questionnaire (PEPPI-5)

Contacts

Public ContactJim Wiegel

Reade Reumatologie

j.wiegel@reade.nl020-2421805

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)