TeleMom - Mixed methods study on the feasibility of telemonitoring of patients with hypertensive disorders in pregnancy (HES)

TeleMom - Mixed methods study on the feasibility of telemonitoring of patients with hypertensive disorders in pregnancy (HES) - TeleMom

Status

Recruiting

Phases

Unknown

Study type

Observational

Source

DRKS

Registry ID

DRKS00036943

Enrollment

Registered

2025-09-11

Start date

2025-09-22

Completion date

Unknown

Last updated

2026-04-27

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

Conditions

Hypertensive disorders of pregnancy

Interventions

Group 1: Potential users of telemonitoring for hypertensive disorders in pregnancy

Eligibility

Sex/Gender

All

Inclusion criteria

Inclusion criteria: Medical professionals (midwives, doctors, nursing staff) - Medical activity in the Perinatal Center of the University Hospital Marburg or in the Marburg-Biedenkopf care region - Sufficient knowledge of German (> B2) Patient representatives - Past or current pregnancy with an HES with treatment in the Perinatal Center of the University Hospital Marburg or in the Marburg-Biedenkopf care region - Sufficient knowledge of German (> B2)

Exclusion criteria

Exclusion criteria: - No private use of smartphones (reason: smartphones are indispensable for the use of the telemonitoring application (data acquisition, communication)).

Design outcomes

Primary

Measure	Time frame
Feasibility (Preclinical Simulation)	—

Secondary

Measure	Time frame
User friendliness	—

Countries

Germany

Contacts

Public ContactSebastian Griewing

Universitäres Perinatalzentrum des Universitätsklinikum Marburg

s.griewing@uni-marburg.de+4964215867079

Outcome results

None listed

Source: DRKS (via WHO ICTRP) · Data processed: May 1, 2026