This was a quantitative and semi-experimental study with the aim of designing and evaluating a device for the “simultaneous measurement of infants’ weight, height, head circumference, temperature, and heart rate”. This digital device was designed and constructed by a team consisting of Mr. Mohammad Eshaghi, a PhD student in general medicine, Mohammad Kozeghari, a PhD in software, Fatemeh Nikpour, a master’s student in epidemiology, and Arzoo Qadimi, a master’s student in pediatric nursing. The device was registered under number 104232 on 18/5/2021.
The constituent parts of this device (
Figure 1) include the following components (different points of the device are numbered in the text and on the figure):
Two-dimensional model of simultaneous measurement of infants’ weight, height, head circumference, temperature, and heart rate digital device
(1) The handle has two sources of ultrasonic waves, the sender and receiver, for measuring the height of the infant. This handle is placed on the infant’s head.
(2) The digital weight sensor is embedded in the body of the device (invisible).
(3) The band is placed around the infant’s head with sources of ultrasonic waves.
(4) The digital temperature sensor site
(5) Heart rate sensor site
(6) Infant body protectors connected to the body
(7) The ultrasound waves are transmitted from section 1 to measure the height after hitting this handle; it is placed under the neonate’s feet.
(8) Rail for height adjustment
(9) Monitoring measured variables
(10) Device on and off switch
(11) Universal Serial Bus (USB) for data transfer to the computer
(12) The body of the device
In the second phase, after designing the device, to evaluate and compare it with the usual method, 100 infants were selected as a sample size from selected hospitals of Shahid Beheshti University of Medical Sciences, Tehran, Iran. G*power software (version) was used to calculate the sample size. Considering α = 0.05 (95% confidence coefficient) and a statistical power of 0.9, the minimum sample size required was 87 subjects, and 100 infants were included.
The data collection tools used included a Wong-Baker Faces scale (
Figure 2) to assess infant distress and a demographic and clinical questionnaire to record growth components and measurement times. The demographic and clinical questionnaire included items such as infant age, gender, duration of intervention using routine methods and the digital device, frequency of infant movements during measurements using both methods and the number of personnel required for measurements for each infant.
After obtaining approval for the research proposal with the ethics code IR.SBMU.RICH.REC.1401.002, data collection took place within June to August 2022. Measurements of height, weight, head circumference, temperature, and heart rate of 100 infants were recorded using two routine methods and a digital device. In addition, the time of the measurement and the infant’s distress score were also recorded in both methods.
The inclusion criteria included the infantile postnatal age between 1 and 365 days, the calmness of the infant at the time of intervention, and the presence of parents. The exclusion criteria included emergency events at the time of the intervention, such as apnea or infant severe restlessness.
At first, the infant’s variables, including weight, height, head circumference, temperature, and heart rate, were measured with routine methods (Zenithmed Baby-s digital scale with a maximum capacity of 25 kg, Marathon meter (150 cm), Sk-30 digital thermometer, and Zenithmed pulse oximeter for infants). The infant’s distress score was determined and recorded with the Wong-Baker Faces scale at the time of measurement, and the number of personnel required to perform measurements for each infant was also recorded.
Subsequently, about 30 minutes after the initial measurements and once the infants had calmed down (as restlessness was one of the exclusion criteria), all measurements were repeated using the digital device, and the results were recorded. The collected data were entered into SPSS software (version 20) for analysis. The data analysis was based on the specific objectives of the study, employing descriptive statistics (mean and frequency percentage) and paired t-tests at a significance level of > 0.05.