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Pilot study: Digital self-monitoring during pregnancy after the expected date of birth

Pilot study: Digital self-monitoring during pregnancy after the expected date of birth - eStork

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
DRKS
Registry ID
DRKS00036585
Enrollment
50
Registered
2025-04-14
Start date
2025-05-01
Completion date
Unknown
Last updated
2025-10-06

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

Conditions

Exceeding the estimated due date

Interventions

Group 1: Intervention group with digital monitoring of fetal heart rate and amniotic fluid volume at home, n=25 Group 2: control group, in which the same ultrasound examinations are performed in the c

Sponsors

ccc. Center for Connected Health
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
18 Years to 40 Years

Inclusion criteria

Inclusion criteria: a) Pregnant woman's wish for outpatient treatment, compliance b) =18 years c) Gestational age =39+0 weeks d) "Low-risk" pregnancy according to maternity guidelines and prenatal examinations according to DEGUM e) Fetal cephalic presentation f) Normal admission status (including CTG, maternal blood pressure, fetal sonography)

Exclusion criteria

Exclusion criteria: a) All high-risk pregnancies according to maternity guidelines or prenatal examinations according to DEGUM b) Placenta previa, low placenta position c) Multiple pregnancy d) Fetal presentation abnormality e) Premature rupture of membranes f) Previous cesarean section g) Fetal growth abnormality h) Severe underlying maternal illness i) Maternal obesity j) Inability to consent

Design outcomes

Primary

MeasureTime frame
Feasibility and Acceptance Feasibility will be assessed after all pregnant women have been included. The quality of ultrasound images and transmission, care requirements and dropout rates will influence this. Acceptance will be assessed for pregnant women in the study arm using a questionnaire after birth or before induction of labor.

Secondary

MeasureTime frame
maternal and child outcome parameters

Countries

Germany

Contacts

Public ContactKurt J. G. Schmailzl

ccc. Center for Connected Health Care

ccc@connectedhealth.com.de+49 3391.39.14980

Outcome results

None listed

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