跳至主要内容
临床试验/NCT05914324
NCT05914324进行中(未招募)不适用

Evaluating Novel Pediatric Pulse Oximeters for Outpatient Child Pneumonia Care in Sub-Saharan Africa

Johns Hopkins University2 个研究点 分布在 1 个国家目标入组 936 人开始时间: 2024年11月4日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
进行中(未招募)
入组人数
936
试验地点
2
主要终点
Proportion of Children with Correct management of oxygen saturation

研究概览

简要总结

The primary objective of this clinical trial is to evaluate the performance of three pulse oximeters during outpatient care within Cape Town, South Africa. This objective will be achieved through generating evidence on how, why, for whom, to what extent and at what cost can paediatric pulse oximetry devices improve the management of hypoxemic children. This will be done with two inter-linked studies:

  • Aim 1: Determine the impact of two novel paediatric pulse oximeter devices on the correct management of hypoxaemia.
  • Aim 2: Describe the burden of hypoxaemia and risks for mortality amongst children presenting with acute respiratory infections in a low-resource setting in Cape Town.

详细描述

Background:

Lower respiratory tract infections (LRI) remain the leading infectious cause of death globally for children younger than five years.1 Alarmingly, >50% of LRI deaths occurred in low and middle-income countries (LMICs) in sub-Saharan Africa, with inequitable distribution both between and within countries.2 Key quality-of-care implementation gaps have hampered the effectiveness of the World Health Organization (WHO) Integrated Management of Childhood Illnesses (IMCI) guidelines used for pediatric LRI care in LMICs.3 Evaluations of Integrated Management of Childhood Illness (IMCI) guidelines have identified inadequate triaging and therefore results in a failure to identify children at higher risk of death. Interventions to improve the sensitivity and specificity of the IMCI approach in identifying severely ill children could improve outcomes. Routine use of pulse oximetry, to non-invasively measure peripheral oxyhemoglobin saturation (SpO2), is poorly implemented at the primary healthcare (PHC) levels in LMICs, and therefore provides one such opportunity to improve IMCI assessments.

Hypoxemia - a low SpO2, is associated with increased mortality in children with LRI(1).4 Hypoxemia prevalence amongst children with pneumonia in African contexts has been estimated at 28%, and in outpatient settings as 23%.5 As hypoxemia is a key mortality risk factor, effectively identifying these children early in the care-seeking pathway is fundamental to reducing mortality in low-resource contexts.6 While SpO2 is recommended by IMCI for children with suspected pneumonia, pulse oximetry devices for measuring SpO2 are not widely implemented in PHCs in LMICs, where most children first access care. In Malawi 16% of nearly 700 outpatient encounters with suspected LRI had a SpO2 measured, and >40% of children eligible for hospitalization were not referred. Since few children have SpO2 collected during outpatient care, referral decisions are largely based on subjective clinical danger signs. This then has knock-on effects on receipt of oxygen treatment.

While pulse oximetry implementation in PHCs has been slow to scale-up, there is evidence of utility and feasibility. In Malawi, healthcare workers successfully measured the SpO2 on 94% of >14,000 children and were >2 times more likely to correctly refer a child when the child's SpO2 was low. This work also demonstrated >60% of hypoxemic children would not have been referred in the absence of an SpO2 measurement.7 One explanation for slow adoption is the lack of appropriate devices, that have been designed specifically for spot-checks amongst children in outpatient LMIC settings - a population with specific oximetry needs. Important features of such a device are being low cost, robust, able to cope with poor perfusion and motion artefact, good battery life and reliable.8

Mobile phones are relatively inexpensive, widely available, and increasingly utilized for healthcare - 'mobile Health (mHealth)', while electronic Health (eHealth) is when electronic services - like the internet - support healthcare. In LMICs mobile phones offer the potential for expanded healthcare access and quality of care both as a medical device and as a platform for eHealth services, such as the digital health management information system (HMIS) used in sub-Saharan Africa - District Health Information Software 2 (DHIS2). Developing a mobile-based pulse oximeter, with interoperability to store and upload data directly into a patients DHIS2 record has the potential to improve the management of paediatric hypoxaemia. The Phefumela Project, meaning "breathe" in a local South African language, will evaluate the impact of two different novel paediatric pulse oximeters, both designed specifically for this population in a high burden setting in South Africa.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Treatment
盲法
Single (Outcomes Assessor)

盲法说明

Due to the nature of the intervention the group who will be blinded are those conducting the analysis. PHC staff, caregivers/patients and study staff in facilities cannot be blinded to the allocation status. Researchers who are responsible for collecting data will be aware of the PHCs allocation. However, for other members of the research team, the investigators will separate those who have access to allocation and those who do not. The key of which PHCs are in which arm will be held by Stellenbosch, and the researcher who will conduct the primary analysis will not have access to this information until after the primary analysis has been completed and also approved by the Study Steering Committee (SSC). This is to ensure internal study integrity and validity.

入排标准

年龄范围
0 Months 至 23 Months(Child)
性别
All
接受健康志愿者

入选标准

  • 0 to <24 months of age inclusive
  • presenting to care for an acute condition the includes observed and/or caregiver history of either cough and/or difficult breathing
  • residing in clinic catchment area
  • caregiver agrees to provide contact details including phone number and/or residential address
  • caregiver agrees to be contacted after two weeks by the study staff
  • caregiver is able and willing to provide written informed consent

排除标准

  • 24 months of age or older
  • presenting to care for a non-acute condition or an acute condition that does not include either observed or caregiver history of cough and/or difficult breathing
  • does not reside in the clinic catchment area
  • caregiver does not agree to provide contact details
  • caregiver does not agree to be contact by study staff after two weeks
  • caregiver unable to provide written informed consent

研究组 & 干预措施

Controls

No Intervention

Controls will be managed routinely by the clinic staff, including the triage and clinical examination pathway through the facility, treatment and referral decisions, all of which can include the standard care device. After the child has had an oxygen saturation measurement, the study data collector will conduct oxygen saturation measurements using the control device and a reference device.

Phefumla

Experimental

Phefumla arm participants will be managed by the clinic staff, including the triage and clinical examination pathway through the facility, treatment and referral decisions, all of which can include the Phefumla device. After the child has had an oxygen saturation measurement, the study data collector will conduct oxygen saturation measurements using the Phefumla device and a reference device. All final patient clinical management decisions will be made based on the reference device measurement.

干预措施: Phefumla device (Device)

LB-01

Experimental

LB-01 arm participants will be managed by the clinic staff, including the triage and clinical examination pathway through the facility, treatment and referral decisions, all of which can include the LB-01 device. After the child has had an oxygen saturation measurement, the study data collector will conduct oxygen saturation measurements using the LB-01 device and a reference device.

干预措施: LB-01 device (Device)

结局指标

主要结局

Proportion of Children with Correct management of oxygen saturation

时间窗: Day 1

The proportion of children aged 0 to \<24 months with acute respiratory infection and (1) a HCW-documented SpO2 and heart rate measured in room air (i.e., off of supplemental oxygen), and (2) an appropriate referral recommendation has been provided by the HCW according to WHO-defined hypoxaemia status (SpO2 \<90% or \>90%) and (3) SpO2 confirmed by study staff measurement with reference device (within 2% SpO2 range above or below the documented SpO2).

次要结局

  • Proportion of Children with Correct SpO2 management (definition 2)(Day 1)
  • Proportion of Children with Correct SpO2 management (definition 3)(Day 1)
  • Proportion of Children with Correct SpO2 management (definition 4)(Day 1)
  • Proportion of Children with Correct SpO2 management (definition 5)(Day 1)
  • Proportion of Children with Correct SpO2 management (definition 6)(Day 15 after enrollment)
  • Communication fidelity as assessed by number of participants who had timely communication(Day 1)
  • Proportion of plausible measurement (Quality measurement)(Day 1)
  • Feasibility as assessed by number of measurement attempts(Day 1)
  • Measurement acceptance as assessed by the proportion of caregivers who permit Sp02 measurement(Day 1)
  • Referral acceptance as assessed by proportion of children who present to hospital(Day 2)
  • Oxygen treatment as assessed by proportion of children who are given oxygen treatment(Day 2)
  • Treatment failure as assessed by proportion of children still feeling sick(Day 15)
  • Hypoxemia prevalence(Day 1)
  • Mortality(Day 15)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (2)

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