Telemonitoring: Patients randomized to intervention group will receive biweeky telephone calls and adaption of antiyhpertensive medication if needed
Study 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
Eligibility
Sex
ALL
Min age
18 Years
Max age
—
Healthy volunteers
No
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
Primary outcome measure(s)
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
Trial sites (1)
Facility
City
Region
Status
Heart Centre Leipzig
Leipzig
Germany
More Heart Center Leipzig - University Hospital trials in Germany
This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.
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