chronical renal insufficiency
Conditions
Interventions
Group 1: Intervention group: The education program consisting of medical and psychological interventions, dietary courses, as well as advises to physical training as parts of a life style modification
Sponsors
Gemeinschaftspraxis
Eligibility
Sex/Gender
All
Age
21 Years to 75 Years
Inclusion criteria
Inclusion criteria: Patients aged 21 to 75 years with a diagnosed, progressive renal insufficiency (serum creatinine between 1,0 and 8,0 mg/dl for women and 1,3 and 8,0 mg/dl for men, determined with clinically routine labor; or a glomerular filtration rate (GFR), calculated with the Modification of Diet in Renal Disease (CKD ) formula with less than 90ml/min/1,73m² body surface, and arterial hypertension that requires drug treatment will be included in the study.
Exclusion criteria
Exclusion criteria: Patients that are not able to receive the education units (e.g. due to acute psychological crisis, due to the need for therapy of serious acute medical Problems as infections or myocardial infarction, due to language problems) and begin of dialysis will be excluded from the study.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| The primary endpoints are the evolution of the renal function with creatinine- GFR-progression, disease-related knowledge and Blood pressure. The moments of measurements are bevor beginning and after of the educational program and one year after the program for the patients who are participating to the educational program. The patients of the controll-group are controlled at the day of recriutement and after one year. | — |
Secondary
| Measure | Time frame |
|---|---|
| The secondary endpoint is a combined endpoint of the trial calculated by the number of patients on dialysis, the number of patients transplanted, doubling of serum creatinine and death in both groups within the follow-up period of one year. | — |
Countries
Germany
Contacts
Public ContactJarmila Mahlmeister
Gemeinschaftspraxis
Outcome results
None listed