MedPath

A Pilot Study for Adaptation of Neospot Device for Health Care at Primary Health Facilities in Kenya

Not Applicable
Not yet recruiting
Conditions
Morbidity
Interventions
Device: Neospot vitals measurement
Registration Number
NCT06132633
Lead Sponsor
Neopenda, PBC
Brief Summary

Neospot device is a 5-in-1 wearable vital signs monitor designed to measure temperature, blood pressure, pulse rate (PR), respiratory rate (RR) and blood oxygen saturation (SPO2). We propose to study the experiences of patients and nurses regarding spot measurement of vital signs at the outpatient department in primary care facilities in Kenya. The study aims to investigate the capability, opportunity, and motivation of nurses to use the Neospot device for vital signs measurement in level 3 facilities in Kenya by validating the accuracy of the Neospot and assessing the experience of patients while using the Neospot, the study also aims to assess the experiences of nurses as they use the Neospot and determine how the Neospot affects their workflow.

Detailed Description

This study intends to investigate the experiences of both nurses and patients in the use of a specific brand of such a device known as the 'neospot' device in various sub county, health centres in Kenya. The study also aims at finding out whether the device affects the rate and efficiency of how nurses work in these facilities.

The study will apply a cross sectional design, three facilities will be used as the sampling frame two urban facilities from Nairobi County and one peri urban rural facility from Kajiado county. The participants will be selected randomly. Data will be obtained from a total of 159 randomly selected patients, all the nurses who will be on duty will also be included as participants in the study and the team leaders will be interviewed as key informants for qualitative data. Quantitative data will be analysed using SPSS version 24 for descriptive and inferential statistics, NVIVO software will be used to analyse the qualitative data to determine the themes. Study Duration: Data collection, analysis and report writing will take 4 ½ months.

Recruitment & Eligibility

Status
NOT_YET_RECRUITING
Sex
All
Target Recruitment
159
Inclusion Criteria
  • Participants between 18 and 70 years of age
  • In stable condition
  • Willing to give consent to participate in the study
Exclusion Criteria
  • Very ill and unstable patients who need emergency care
  • Patients with medical conditions that are characterized by rapid changes in vital signs such as thyroid disorders
  • Patients who have skin lesions on the forehead where the device is to be fixed

Study & Design

Study Type
INTERVENTIONAL
Study Design
SINGLE_GROUP
Arm && Interventions
GroupInterventionDescription
Neospot Vitals MeasurementNeospot vitals measurementNeospot is a 5-in-1 wearable vitals measurement device designed to measure temperature, blood pressure, pulse rate, respiratory rate and blood oxygen saturation. For the standard of care vitals measurement, conventional vital signs will be measured using mercury blood pressure cuffs and infrared or mercury thermometers for blood pressure and temperature respectively, pulse oximeter for oxygen saturation and a 1-minute count of heart rate and breathing rate.
Primary Outcome Measures
NameTimeMethod
Capability, opportunity and motivation of nurses to use the Neospot device for vital signs measurementFrom enrolment, monitoring, data extraction and analysis over a period of 4 months

Number of nurses reporting positive experiences and improved workflow as a result of utilizing the neospot product as responded in surveys

Secondary Outcome Measures
NameTimeMethod
Acceptability of Neospot device by nurses for adoption in health facilitiesFrom enrolment, monitoring, data extraction and analysis over a period of 4 months

Number of nurses willingness to adopt the use the Neospot device as their primary vital sign measurement tool post utilization, determined through surveys

Effects of Neospot vitals measurement device on nurses' workflowFrom enrolment, monitoring, data extraction and analysis over a period of 4 months

Number of nurses reporting positive impact of the Neospot device on efficiency and improved workflow through surveys

Accuracy of vitals measurement of Neospot device compared to traditional equipmentFrom enrolment, monitoring, data extraction and analysis over a period of 4 months

We want to validate the accuracy of the Neospot device to measure temperature, SPO2, pulse rate and respiratory rate by comparing similarities and differences to the traditional devices vital signs readings

Experiences of patients using the Neospot vitals measurement deviceFrom enrolment, monitoring, data extraction and analysis over a period of 4 months

Number of patients reporting positive experience with our Neospot device through surveys

Trial Locations

Locations (1)

Langata, Kianda 42 and Matasia Health Centre

🇰🇪

Nairobi, Kenya

© Copyright 2025. All Rights Reserved by MedPath