Rheumatoid Arthritis M05 M06
Conditions
Interventions
Group 1: Structured assessment and classification of comorbidities and risk factors by a rheumatology nurse specialist ahead of consultation by the rheumatologist.
Group 2: Standard of care
Sponsors
AbbVie Deutschland GmbH & Co. KG
Eligibility
Sex/Gender
All
Age
18 Years to No maximum
Inclusion criteria
Inclusion criteria: Adults with Minimum Age of 18 years, capable of giving informed consent and diagnosis of rheumatoid Arthritis and stable on DMARDs or bDMARDs for at least three months.
Exclusion criteria
Exclusion criteria: Change of disease-modifying base therapy (dose, substance or interval) within the last three months.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Primary observational endpoint is the Change of the risk Profile of patients within 12 months after the first structured assessment.The risk Profile will be judged by a new composite score, consisting of the categorized results of established and validated risk assessment questionnaires. | — |
Secondary
| Measure | Time frame |
|---|---|
| Difference in the 12-month change of the risk profile between arm 1 and arm 2. | — |
Countries
Germany
Contacts
Public ContactRolf Hecker
Abbvie Deutschland GmbH & Co. KG
Outcome results
None listed