M06
Conditions
Interventions
Group 1: 1 study arm = intervention group
Probands with rheumatoid arthritis using the Fimo-Health App
Sponsors
Uniklinik Erlangen
Eligibility
Sex/Gender
All
Age
18 Years to No maximum
Inclusion criteria
Inclusion criteria: Patients with rheumatoid arthritis who fulfill the ACR/EULAR classification crite.ria, written informed consent.
Exclusion criteria
Exclusion criteria: No signed declaration of consent, change of medication in the last 3 months.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| 1. Can quality of life be improved in patients with rheumatoid arthritis using the Fimo Health App? 2. How does fatigue change when using the Fimo Health app in patients with rheumatoid arthritis? 3. Can pain be reduced in patients with rheumatoid arthritis using the Fimo Health app? | — |
Secondary
| Measure | Time frame |
|---|---|
| 1. Is there an improvement in health and exercise competency using the Fimo-Health app in patients with rheumatoid arthritis? 2. How does the Fimo-Health app affect fear of movement in patients with rheumatoid arthritis? 3. Is the Fimo-Health app user-friendly for patients with rheumatoid arthritis? 4. What is the acceptance of the Fimo-Health app among patients with rheumatoid arthritis? 5. Is the FimoHealth app used regularly and what content is the main focus? | — |
Countries
Germany
Contacts
Public ContactHarriet Morf
Uniklinik
Outcome results
None listed