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Prospective randomized, group-controlled pilot study 2021-2022 of clinical causality, efficacy and safety of the CE-marked app "mediteo m+"

Prospective randomized, group-controlled pilot study 2021-2022 of clinical causality, efficacy and safety of the CE-marked app "mediteo m+" - mediteo 2021-2022

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
DRKS
Registry ID
DRKS00026278
Enrollment
80
Registered
2023-07-24
Start date
2022-02-11
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

Drug Adherence

Interventions

Group 1: mediteo +1 app Group 2: TAU, Therapy as usual

Sponsors

Mediteo GmbH
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 100 Years

Inclusion criteria

Inclusion criteria: Chronic medication

Exclusion criteria

Exclusion criteria: Serious internal, neurological, vision disease

Design outcomes

Primary

MeasureTime frame
Actual tablet count divided by target tablet count

Secondary

MeasureTime frame
Blood pressure

Countries

Germany

Contacts

Public ContactHans-Peter Zenner

Clinical Research OrganizationHP Zenner Clinical GmbH&CoKG

office@hpzenner.de+49707149645

Outcome results

None listed

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