Telemonitoring in Arterial Hypertension

N/AActive Not RecruitingNCT07049289

Heart Center Leipzig - University Hospital60 enrolled

Overview

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

Study Type

INTERVENTIONAL

Allocation

RANDOMIZED

Purpose

TREATMENT

Masking

NONE

Enrollment

Conditions

Arterial Hypertension Uncontrolled Hypertension

Interventions

TelemonitoringOTHER

Patients randomized to intervention group will receive biweeky telephone calls and adaption of antiyhpertensive medication if needed

Eligibility

Sex: ALLMin age: 18 Years

Medical Language ↔ Plain English

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

Locations (1)

Heart Centre Leipzig

Leipzig, Germany

Outcomes

Primary Outcomes

Time in blood pressure target range from randomization through 6 months

Time in target range of each blood pressure measurement in first 6 months between control and intervention group

Time frame: 6 months

Secondary Outcomes

Time in target range months 6 to 12

Time in target range of each blood pressure measurement between control and intervention group from months 7 to 12

Time frame: 6 months (7-12 months)

Medication adherence as assessed by blood/urine sampling after 6 and 12 months

Time frame: 0, 6 and 12 months

Data from ClinicalTrials.gov

This platform is for informational purposes only and does not constitute medical advice. Always consult a qualified healthcare professional.