Ability of the Polar Wearables to Detect Fetal Heart Rate - Pilot Clinical Study

Status

Completed

Phases

Unknown

Study type

Observational

Source

ClinicalTrials.gov

Registry ID

NCT06683183

Enrollment

Registered

2024-11-12

Start date

2025-02-19

Completion date

2025-04-11

Last updated

2025-04-18

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

Conditions

Fetal Heart Rate Tracing

Brief summary

The aim of this clinical pilot study is 1. to evaluate the ability of the wearables to detect fetal heart rate 2. to evaluate the ability to distinguish the fetal ECG from the ECG of the mother The participating pregnant women will wear the Polar wearables (chest band, smart watch, arm band) for 15 minutes during of which, the data will be collected with all three wearables and patient monitor (reference device). The data from the wearables will be compared with the patient monitor data referred as golden standard. Background information will be collected with questionnaires from the participants. The data collection will be conducted in hospital environment.

Interventions

None listed

Study design

Observational model

COHORT

Time perspective

PROSPECTIVE

Eligibility

Sex/Gender

FEMALE

Healthy volunteers

Inclusion criteria

* duration of pregnancy at least 29+0 weeks * single pregnancy * age at least 18 years * ability to participate in Finnish. No

Design outcomes

Primary

Measure	Time frame
Fetal heart rate	15 minute data collection

Countries

Finland

Outcome results