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Testing A Visual Thermometer in Newborns and Young Infants

Testing A Visual Thermometer in Newborns and Young Infants

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT05609292
Enrollment
120
Registered
2022-11-08
Start date
2022-12-05
Completion date
2023-09-30
Last updated
2023-11-28

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

Conditions

Hyperthermia, Hypothermia

Keywords

temperature monitoring, liquid crystal thermometer, hypothermia, hyperthermia, LCTD, infant temperature, infant hyperthermia, infant hypothermia, neonate hyperthermia, neonate hypothermia, neonate temperature

Brief summary

Severe neonatal jaundice and acute bilirubin encephalopathy are a major cause of death and disability among newborns in LMICs. Filtered sunlight phototherapy (FSPT) was developed, tested and shown to be safe and efficacious in the treatment of jaundice, because effective electric-powered conventional phototherapy is often unavailable10,11. However, FSPT currently requires at least hourly temperature monitoring by healthcare providers (HCPs) because infants receiving FSPT are prone to both hypothermia and hyperthermia. 20 years ago, a liquid crystal thermometer, ThermospotTM (Maternova, Providence, RI) was developed primarily for use in LMICs. It was designed to detect hypothermia and is most sensitive in cold infants and not as sensitive as needed for detecting hyperthermia or fever. The purpose of this pilot study is to determine the accuracy and useability of this LCTD for a wider spectrum of temperatures when used in a large group of infants in a high-income country. If the device performs well in this study, we plan to study it in a low- and middle-income country in Africa.

Interventions

DEVICEobservational

Infants will get their temperature measured with the liquid crystal thermometer. We are not providing any interventions as they will be in the care of a healthcare team.

Sponsors

University of Minnesota
Lead SponsorOTHER

Study design

Observational model
CASE_CROSSOVER
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
0 Months to 6 Months
Healthy volunteers
Yes

Inclusion criteria

* Infants 0-6 months (\<7 months) presenting to Masonic Emergency Room or inpatient ward, their parent or caregiver who provide verbal consent in English or through a medical interpreter.

Exclusion criteria

* Any infant undergoing active resuscitation * any infant for whom physician deems study enrollment would interfere with their care * any infant whose parents or caregiver decline enrollment * any nurse or other healthcare provider who declines participation * Parents who do not understand English, and do not have a medical interpreter at the bedside.

Design outcomes

Primary

MeasureTime frameDescription
Accuracy of the liquid crystal thermometer with measuring a temperaturebaselinedetermining the accuracy of the LCTD in estimating the temperature of infants 0-6 months presenting to the emergency room for treatment
Parents/Caregivers and Healthcare provider accuracy in evaluating the infant temperaturebaselineOur secondary endpoint is determining parents/caregivers and healthcare provider accuracy in evaluating the temperature of their infant or the infant they are caring for and determining the category of the temperature.

Countries

United States

Outcome results

None listed

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