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

NCT06683183 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 11

Last updated 2025-04-18

No results posted yet for this study

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.

Conditions

  • Fetal Heart Rate Tracing

Sponsors & Collaborators

  • Polar Electro Oy

    collaborator UNKNOWN

  • Anna Axelin

    lead OTHER

Eligibility

Sex
FEMALE
Healthy Volunteers
No

Timeline & Regulatory

Start
2025-02-19
Primary Completion
2025-04-11
Completion
2025-04-11

Countries

  • Finland

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT06683183 on ClinicalTrials.gov