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Use Of An In-Home Non-Stress Test Device For Remote Fetal Monitoring

Use Of An In-Home Non-Stress Test Device For Remote Fetal Monitoring In A Local High-Risk Obstetric Population

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02379351
Enrollment
60
Registered
2015-03-04
Start date
2015-07-31
Completion date
2017-05-31
Last updated
2025-03-19

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

Conditions

High Risk Pregnancy

Keywords

Non-stress Test, Fetal Monitoring, Telemedicine

Brief summary

Non-stress tests (NSTs) are used to monitor the health of babies during pregnancy. These tests are currently conducted in clinics and hospitals. This requires travel to a clinic or hospital, sometimes multiple times per week, in order to receive these tests. Technology has been developed that now allows for NSTs to be done in other locations, including home or work. The Airstrip® Sense4Baby™ NST device has been FDA-approved for use by obstetricians in clinical and hospital settings. The investigators are evaluating the use of the Airstrip® Sense4Baby™ NST device in out-of-hospital settings. The investigators would like to know if this type of monitoring is feasible and acceptable to patients and physicians.

Detailed description

Phase I of this study enrolls pregnant women with physician-ordered twice-weekly NSTs scheduled in the OB Diagnostic Center at the University of Utah Hospital. Participants receive an in-clinic NST with the Airstrip® Sense4Baby™ device, are taught how to use the device, and asked to demonstrate their ability to use the device. Once the participant successfully demonstrates use of the monitor the device is given to the participant to use at the scheduled time each week. Patients receive educational materials, including a visuals-enhanced, short quick start guide. For her remote NST monitoring, the patient will receive a virtual NST appointment. At the time of the scheduled appointment, the patient will apply the monitor and the NST will be read by the mid-level provider staffing the testing center after a thirty-minute strip has been recorded and transmitted to the database. The NST will also be interpreted by the maternal-fetal medicine physician, according to the established workflow. The patient will be notified of the result by a telephone call from the mid-level provider and appropriate follow-up arranged according to the NST management algorithm developed for this study. If the patient has trouble with using the device at home, the patient will be able to talk with the mid-level provider via telephone to troubleshoot issues. The patient will also continue to receive an NST in clinic weekly. These NST schedules will be repeated on a weekly basis until delivery or until the provider discontinues the NST order. Patients will be contacted after delivery to assess overall satisfaction with the NST at home versus in clinic. Phase II of this study will enroll the same patient population (pregnant women with physician-ordered twice-weekly NSTs scheduled). Participants in Phase II may receive NSTs up to twice weekly at home. During regularly scheduled obstetric visits (every 1 to 2 weeks depending on gestational age and circumstances), NSTs will be performed on site. However, we will remove the requirement for once weekly on-site testing at the University of Utah Hospital. The requirement to be within a 60-mile radius of University Hospital will be removed for Phase II participants. Instead, the requirement will be to be within a 60-mile radius of a hospital with an obstetric unit. Patients will be contacted after delivery to assess overall satisfaction with the NST at home versus in clinic.

Interventions

DEVICEIn-Home Non-Stress Test Device

Airstrip® Sense4Baby™

Sponsors

University of Utah
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
SUPPORTIVE_CARE
Masking
NONE

Eligibility

Sex/Gender
FEMALE
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

Target population: The target population is high-risk pregnant women. Accessible population: The accessible population is high-risk obstetric patients receiving care throughout the University of Utah Healthcare system and who receive their NSTs at MFDC. Inclusion Criteria (Phase I): * Singleton gestation * Estimated gestational age of 32 0/7 -37 6/7 weeks * Physician order for twice weekly NSTs * Live within 60-mile radius of the University of Utah University Hospital * Reliable access to and connectivity with wireless Internet * Reliable for communication and follow-up

Exclusion criteria

(Phase I: * Multifetal gestation * Maternal age less than 18 * Plans to move prior to end of pregnancy * No or limited access to internet and/or phone Inclusion Criteria (Phase II): * Singleton gestation * Estimated gestational age of 32 0/7 -37 6/7 weeks * Physician order for twice weekly NSTs * Live within 60-mile radius of the University of Utah University Hospital or a hospital with an obstetric inpatient unit * Reliable access to and connectivity with wireless Internet * Reliable for communication and follow-up

Design outcomes

Primary

MeasureTime frameDescription
Number of Interpretable Results (Participants Who Used the NST Device Correctly)Enrollment at 32 0/7 - 37 6/7 weeks gestation through deliveryNumber of Interpretable Results (Participants who Used the NST Device Correctly)

Secondary

MeasureTime frameDescription
Provider Satisfaction With Remote NST Compared to On-site NST2 YearsProvider Satisfaction With Remote NST Compared to On-site NST

Countries

United States

Participant flow

Participants by arm

ArmCount
In-Home Non-Stress Test Device
Patients with physician-ordered twice-weekly NSTs scheduled in the OB Diagnostic Center at University of Utah Hospital. Participants utilized the device on a weekly basis (at home) until the time of delivery. Participants also received an in clinic NST once a week. In-Home Non-Stress Test Device: Airstrip® Sense4Baby™
60
Total60

Baseline characteristics

CharacteristicIn-Home Non-Stress Test Device
Age, Categorical
<=18 years
0 Participants
Age, Categorical
>=65 years
0 Participants
Age, Categorical
Between 18 and 65 years
60 Participants
Age, Continuous31 years
Race (NIH/OMB)
American Indian or Alaska Native
1 Participants
Race (NIH/OMB)
Asian
2 Participants
Race (NIH/OMB)
Black or African American
1 Participants
Race (NIH/OMB)
More than one race
0 Participants
Race (NIH/OMB)
Native Hawaiian or Other Pacific Islander
2 Participants
Race (NIH/OMB)
Unknown or Not Reported
3 Participants
Race (NIH/OMB)
White
51 Participants
Region of Enrollment
United States
60 participants
Sex: Female, Male
Female
60 Participants
Sex: Female, Male
Male
0 Participants

Adverse events

Event typeEG000
affected / at risk
deaths
Total, all-cause mortality
0 / 60
other
Total, other adverse events
0 / 60
serious
Total, serious adverse events
0 / 60

Outcome results

Primary

Number of Interpretable Results (Participants Who Used the NST Device Correctly)

Number of Interpretable Results (Participants who Used the NST Device Correctly)

Time frame: Enrollment at 32 0/7 - 37 6/7 weeks gestation through delivery

Population: Patients with physician-ordered twice-weekly NSTs scheduled in the OB Diagnostic Center at University of Utah Hospital. Participants were trained by clinicians at the hospital and then used the device on a weekly basis (at home) until the time of delivery. Participants will also receive an in clinic NST once a week.

ArmMeasureCategoryValue (COUNT_OF_UNITS)
Experimental: In-Home Non-Stress Test DeviceNumber of Interpretable Results (Participants Who Used the NST Device Correctly)Number of Interpretable Results107 Remote NST's Completed
Experimental: In-Home Non-Stress Test DeviceNumber of Interpretable Results (Participants Who Used the NST Device Correctly)Number of Non-Interpretable Results1 Remote NST's Completed
p-value: 0.1Chi-squared
Secondary

Provider Satisfaction With Remote NST Compared to On-site NST

Provider Satisfaction With Remote NST Compared to On-site NST

Time frame: 2 Years

Population: Referring and NST Reading Providers

ArmMeasureValue (COUNT_OF_PARTICIPANTS)
Experimental: In-Home Non-Stress Test DeviceProvider Satisfaction With Remote NST Compared to On-site NST21 Participants
p-value: <0.01Chi-squared

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026