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Digital lifestyle intervention solution for hypertension

Digital lifestyle intervention solution for hypertension

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
DRKS
Registry ID
DRKS00030109
Enrollment
100
Registered
2022-09-01
Start date
2022-09-12
Completion date
Unknown
Last updated
2025-04-07

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

I10.9

Interventions

Group 1: Intervention group: immediate access to the app actensio after confirmation of a hypertension diagnosis through a seven-day hypertension diary (morning and evening measurement of systolic and

Sponsors

mementor DE GmbH
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: - Consent to participate in the study - Age >= 18 years - Meet criteria for hypertension (=135/90mmHg & ) - Internet access - Able to complete data collection and intervention - Motivated to make lifestyle changes - No or stable antihypertensive medication (i.e. no change in the last 3 months) - Possession of a blood pressure monitor

Exclusion criteria

Exclusion criteria: - Resistant hypertension (home BP =175mmHg or =4 different classes of blood pressure medication). - Reasons of safety (e.g. pregnancy, diabetes requiring insulin) - Life expectancy <12 months - One person per household (contamination) - Cardiovascular event within the last 6 months (e.g. stroke, heart attack, cerebral haemorrhage) - Cancer diagnosis or acute treatment with chemotherapy/immunosuppressants - Planned health/medication plan change (in the next 3 months) - Planned hospitalisation (in the next 3 months)

Design outcomes

Primary

MeasureTime frame
Comparison of actensio + care as usual versus care as usual on systolic blood pressure. The mean systolic blood pressure at baseline, measured over seven days in the morning and evening at home, will be compared with the mean systolic blood pressure measured over seven days in the morning and evening at home after three months after inclusion. Data are collected via a digital blood pressure diary

Secondary

MeasureTime frame
Comparison of actensio + care as usual versus care as usual on diastolic and mean blood pressure and pulse, and the PAM-13 patient activation questionnaire.

Countries

Germany

Contacts

Public ContactAlina Wildenauer

RuhrlandklinikZentrum für Schlaf- und Telemedizin

alina.wildenauer@rlk.uk-essen.de0201 4334926

Outcome results

None listed

Source: DRKS (via WHO ICTRP) · Data processed: Feb 4, 2026