Arterial Hypertension, Uncontrolled Hypertension
Conditions
Brief summary
Prospective, randomized trial to assess the effects of a telemedical approach of antihypertensive treatment in comparison with standard care. Total patient number: 60 patients. * Intervention group: biweekly telephone calls * Control group: standard of care
Interventions
Patients randomized to intervention group will receive biweeky telephone calls and adaption of antiyhpertensive medication if needed
Sponsors
Study design
Eligibility
Inclusion criteria
1. Confirmed arterial hypertension with systolic or diastolic blood pressure \>140/90 mmHg in standardized office blood pressure measurement 2. Treatment with 1 to ≤4 antihypertensive drug classes 3. Age \>18 years 4. Written informed consent
Exclusion criteria
1. Pregnancy 2. Participation in other randomized trials 3. Patients under legal supervision or guardianship
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Time in blood pressure target range from randomization through 6 months | 6 months | Time in target range of each blood pressure measurement in first 6 months between control and intervention group |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| Time in target range months 6 to 12 | 6 months (7-12 months) | Time in target range of each blood pressure measurement between control and intervention group from months 7 to 12 |
| Medication adherence as assessed by blood/urine sampling after 6 and 12 months | 0, 6 and 12 months | Medication adherence as assessed by blood/urine sampling after 6 and 12 months |
Countries
Germany