- BMBF
ICON
Inception Cohort of newly diagnosed patients with juvenile idiopathic arthritis
The aim of the project was to form a cohort of children and adolescents with newly diagnosed juvenile idiopathic arthritis (JIA) and peers for comparison. Through the prospective, standardized observation of the patient group, new insights were gained into the course of the disease, prognosis, indicators of disease progression, the health care situation, and socioeconomic aspects of JIA. The knowledge gained will help to further improve the care of JIA patients and to minimize long-term consequences of the disease.
2009-2022
Head of project
Current projects
Data from the ICON early cohort are currently being used to
- estimate the health care costs of JIA (PAVE)
- examine the familial burden of the disease (PAVE)
- analyze the utilization of and satisfaction with health care services over time (DZKJ)
- to determine the progression of health and risk behavior in adolescents with juvenile idiopathic arthritis compared to controls (DZKJ)
- to compare the life satisfaction of adolescents with JIA with that of age-appropriate controls
- to record the emotional strain and health-related quality of life of children and adolescents with juvenile idiopathic arthritis over the course of the disease and to determine associated factors
- to examine differences between the perception of disease activity in JIA by children, parents and doctors and to identify factors that explain these differences (DZKJ)
- to determine drop-out rates over time and to understand the reasons for them (DZKJ)
Team
AG Minden
