A Mixed Methods Study to Explore the Feasibility of a Novel Continuous Fetal Monitoring Device
NCT ID: NCT03370822
Last Updated: 2018-05-02
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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COMPLETED
20 participants
OBSERVATIONAL
2016-06-22
2017-12-31
Brief Summary
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Detailed Description
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A recent study found that 45.1% of surveyed clinicians thought that a continuous fetal monitor would be beneficial to their practice, although 81.7% also expressed concerns about the utility and clinical implementation of such a device. The Monica AN24 monitor is a novel continuous fetal monitoring device which records the fetal electrocardiogram (fECG) via trans-abdominal electrodes. Monica AN24 has been shown to have good recording quality though one study reported an association between recording quality and gestational age. The effect of the device on maternal anxiety is not known. All studies assessing acceptability of the device to women have focused on the intrapartum period or during induction of labor. Consequently, a prospective observational cohort study is needed to assess the acceptability of the Monica AN24 device in the context of antenatal care, as is further exploration of factors affecting recording quality of the Monica AN24 device.
Conditions
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Study Design
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COHORT
PROSPECTIVE
Study Groups
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Study Participants
Women who have continuous fetal monitoring using the MONICA AN24 device. The MONICA AN24 is a wearable monitor with five adhesive electrodes placed on the mother's abdomen. This records the fetal heart rate, maternal heart rate and uterine contractions.
MONICA AN24 device
Application of MONICA AN24 device and recording for the longest period of fetal heart rate recording possible (limited by battery life)
Interventions
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MONICA AN24 device
Application of MONICA AN24 device and recording for the longest period of fetal heart rate recording possible (limited by battery life)
Eligibility Criteria
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Inclusion Criteria
* No abnormality identified on ultrasound scan of fetal biometry and umbilical and fetal Doppler indices
* Gestational age \>24 weeks
* Able to give informed consent
Exclusion Criteria
* Maternal age \<18 years
* Individuals who do cannot speak or do not understand fluent English
* Individuals unable to give informed consent
* Women in active labour
18 Years
50 Years
FEMALE
No
Sponsors
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University of Manchester
OTHER
Responsible Party
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Dr Alexander Heazell
Professor of Obstetrics
Locations
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Central Manchester University Hospitals NHS Foundation Trust
Manchester, , United Kingdom
Countries
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Other Identifiers
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201920
Identifier Type: -
Identifier Source: org_study_id
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