Tools for the Integrated Management of Childhood Illness: Cross-country Quasi-experimental Pre-post Study in Kenya and Senegal

Pneumonia Clinical Trial

— TIMCI  

Official title:

Tools for the Integrated Management of Childhood Illness: Evaluation of Pulse Oximetry and Clinical Decision Support Algorithms in Primary Care. Cross-country Quasi-experimental Pre-post Study, With Embedded Mixed Methods Studies, Cost and Modelled Cost-effectiveness in Kenya and Senegal

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT05065320
• Other study ID #: ERC.0003406
• Status: Completed
• Start date: August 16, 2021
• Est. completion date: March 31, 2023

Study information

• Verified date: November 2022
• Source: Swiss Tropical & Public Health Institute
• Contact: n/a
• Is FDA regulated: No
• Study type: Observational [Patient Registry]

Clinical Trial Summary

By introducing pulse oximetry, with or without clinical decision support algorithms, to primary care facilities in India, Kenya, Senegal and Tanzania, the Tools for Integrated Management of Childhood Illness (TIMCI) project aims to contribute to reducing morbidity and mortality for sick children under-five while supporting the rational and efficient use of diagnostics and medicines by healthcare providers. The multi-country, multi-method evaluation aims to generate evidence on the health and quality of care impact, operational priorities, cost and cost-effectiveness of introducing these tools to facilitate national and international decision-making on scale-up.

Description:

This registry entry describes the quasi-experimental pre-post studies conducted in Kenya and Senegal. In India and Tanzania, pragmatic cluster randomised controlled trials (RCTs) are conducted (NCT04910750). These studies evaluating health, clinical and quality of care impact are complemented by embedded multi-method studies in all countries, including modified Service Provision Assessments, facility-based process mapping and time-flow studies, in-depth interviews (IDIs) with caregivers and healthcare providers, online key stakeholder surveys and key informant interviews, routine data review, and an economic evaluation. We enrol sick children 0 to 59 months of age attending government primary care facilities in before and after implementation of pulse oximetry and CDSA. Interventions are implemented with a package of training on the use of devices and refresher IMCI, supportive supervision, operational support and community engagement. As part of the intervention, facilities are provided with handheld, UNICEF-approved, pulse oximeters along with guidance and training for healthcare providers. In Senegal, healthcare providers are advised to measure oxygen saturation (SpO2) on all children under 2 months of age, all children 2 to 59 months of age with cough or difficulty breathing or with signs of moderate or severe disease based on Integrated Management of Childhood Illness (IMCI); in Kenya, healthcare providers are advised to measure oxygen saturation for all sick children. Providers are advised to urgently refer children with SpO2 <90% in Kenya and <92% in Senegal. The tablet-based CDSA provides step-by-step support to healthcare providers through consultations, providing national guideline-based recommendations on assessment, diagnosis and treatment based tailored to the individual child based on information entered by the provider. Following training, providers are advised to use CDSA for all consultations with sick children under 5 years of age. Sociodemographic and clinical data are collected from caregivers and records of enrolled sick children at study facilities, with phone follow-up on Day 7. Two primary outcomes are assessed for the quasi-experimental pre-post study: referrals to a higher level of care at Day 0 consultation; and antibiotic prescriptions on Day 0. These reflect the aim that the intervention increases detection of severe disease, and therefore increasing referral, whilst promoting antimicrobial stewardship, and therefore reducing antibiotic prescription. Secondary outcomes, relating to hypoxaemia, hospitalisation, referral, antimicrobial prescription, follow-up, health status are further detailed in the attached full protocol and statistical analysis plan available. The pre-post study sample size was originally estimated for a planned 15 month study, with 3 months pre- (Q1) and 12 months post-intervention (Q2-5), with comparison of Q1 and Q5 for the primary outcome. Calculations were based on detecting a ≥50% increase in Day 0 referrals (from 3%, based on DHIS2, SPA and facility estimates), with 80% power, 0.05 alpha and ICC of 0.00547. A relatively large detectable difference was chosen given that a relatively high proportion of referrals may not be completed.5 46 Day 0 referrals, rather than antibiotic prescriptions (with baseline estimated at 60% with ICC 0.05), drove the sample size calculation. We estimated needing 17 facilities, recruiting an average of 690 children per facility per 3-month period in Kenya, and 18 facilities recruiting 510 children per facility per period in Senegal. Following lower than anticipated recruitment in the baseline of the pre-post study, sample size was re-evaluated resulting in a decision to add two facilities per country, extend the baseline (to 6-7 months), and reduce the post-intervention period (to 9-10 months). A minimum of 7429 and 6760 children were estimated to be needed in each period in Kenya and Senegal respectively, with recruitment continuing after meeting the minimum sample size in order to allow for description of changes over time and with overlapping seasonal periods, in line with the intention of the original design. Study approval has been granted by all relevant institutional review boards, national and WHO ethical review committees. Findings will be shared with communities, healthcare providers, Ministries of Health and other local, national and international stakeholders to facilitate evidence-based decision-making on scale-up.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 51590
• Est. completion date: March 31, 2023
• Est. primary completion date: March 31, 2023
• Accepts healthy volunteers: Accepts Healthy Volunteers
• Gender: All
• Age group: 1 Day to 5 Years

Eligibility

Inclusion Criteria:

• Children 0-59 months of age for whom caregivers provide consent
• Consulting for an illness, or reported to be unwell when attending for a routine visit (e.g. vaccination, growth or chronic disease monitoring)

Exclusion Criteria:

• Children in the immediate post-natal period or first day of life
• Attending for a consultation related to trauma only (including new and follow-up presentations for burns, injuries, wounds)
• Admitted within an inpatient part of the facility (including neonates delivered at the facility admitted with their mother)
• Enrolled in the study within the preceding 28 days at any study facility

Related Conditions & MeSH terms

• Decision Support Systems, Clinical
• Hypoxia
• Pneumonia
• Primary Health Care

Locations

Country	Name	City	State
Kenya	University of Nairobi	Nairobi
Senegal	UCAD	Dakar

Sponsors (5)

Lead Sponsor	Collaborator
Swiss Tropical & Public Health Institute	Burnet Institute, Cheikh Anta Diop University, Senegal, PATH, University of Nairobi

Countries where clinical trial is conducted

Kenya,  Senegal, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Proportion of children referred by a primary care healthcare provider to a higher level of care (either to a hospital or to an inpatient part of a larger primary healthcare facility) at Day 0 consultation	The denominator will be all children recruited. Only urgent referrals will be considered.	At time of enrolment
Primary	Proportion of children prescribed an antibiotic at Day 0	Only antibacterials for systemic use will be taken into account for the definition of antibiotics. All children recruited will be counted in the denominator.	At time of enrolment
Secondary	Proportion of children with a severe complication (death or secondary hospitalisation) by Day 7	Secondary hospitalisation refers to any delayed hospitalisation (occurring at any point greater than 24 hours after Day 0 consultation) and any hospitalisation occurring without referral. The denominator is all enrolled children..	From enrolment up to 7 days after
Secondary	Proportion of children admitted to hospital within 24 hours of the Day 0 primary care consultation and as a result of a referral	This is used as a proxy for 'appropriate referral' of children, as those with severe disease should generally be admitted to hospital. The denominator for this outcome is also all children enrolled in the study, rather than only referred children. This is because the proportion of referred children that are admitted may be high in routine care, in the context of an inappropriately low referral rate. The aim of the intervention is therefore to increase the overall referral rate of children with severe disease. Hospital admission is chosen as the proxy of severe disease rather than using primary care classification of severe disease, as there are inadequacies in the classification of severe disease in routine practice. A child will be considered admitted to hospital 24hrs of Day0 consultation if the date of hospitalization is the same as Day0 date or is one day after Day0 date.	From enrolment up to 1 day after
Secondary	Proportion of children who completed referral, as reported at day 7 follow-up	Only urgent referrals will be considered. A referral will be considered completed if a child attended a hospital, whether was admitted or not. A window of +3 days from Day 7 is considered.	From enrolment up to 10 days after
Secondary	Proportion of children cured (defined as caregiver reported recovery from illness) by Day 7	The denominator will be all children recruited. A window of +3 days from Day 7 is considered.	From enrolment up to 10 days after
Secondary	Proportion of children with non-severe disease referred to a higher level of care on Day 0	Only urgent referrals will be considered. Only urgent referrals will be considered.	At time of enrolment
Secondary	Average length of stay (in days) of children admitted to hospital	If a child is hospitalised twice, the first hospitalization will be used and second hospitalizations will be reported separately. The denominator will be all hospitalised children. This is not a time-to-event outcome measure, as it will be analysed as a continuous variable.	From hospital admission to discharge
Secondary	Proportion of children prescribed a diagnosis-appropriate antibiotic	Appropriateness of antibiotic prescription in relation to diagnosis will be evaluated as: diagnosis for which a systemic antibiotic was indicated and a systemic antibiotic was prescribed; diagnosis for which a systemic antibiotic was not indicated and systemic antibiotic was prescribed; first-line (or second-line) antibiotics were prescribed according to recommendations for IMCI diagnoses for which specific antibiotic(s)are indicated Diagnoses will be classified according to whether systemic antibiotics are indicated, based on IMCI and other relevant national guidelines as used for the CDSA.	At time of enrolment
Secondary	Proportion of febrile children tested for malaria at Day 0	A child will be considered to be febrile if history of fever was reported by the caregiver before the consultation or temperature was recorded to be above or equal 37.5 C°. Only febrile children will be counted in the denominator.	At time of enrolment
Secondary	Proportion of malaria positive children prescribed an antimalarial	Only children with a positive malaria test result will be counted in the denominator.	At time of enrolment
Secondary	Proportion of malaria negative children prescribed an antimalarial	Only children with a negative malaria test result will be counted in the denominator.	At time of enrolment
Secondary	Proportion of untested children prescribed an antimalarial	Only children untested for malaria will be counted in the denominator.	At time of enrolment
Secondary	Proportion of children with severe, moderate and mild hypoxaemia, adjusted for sites at high altitude	The following SpO2 values ranges will be used: SpO2 < 90%, 90% = SpO2 < 92% and 92% = SpO2 < 94%. All children recruited will be in the denominator.	At time of enrolment
Secondary	Proportion of children with hypoxaemia (according to differing cut-offs) with severe complication	The following SpO2 values ranges will be used: SpO2 < 90%, 90% = SpO2 < 92% and 92% = SpO2 < 94%, spurious values and missing values. Each SpO2 group will be the denominator of each proportion.	At time of enrolment
Secondary	Proportion of children with severe hypoxaemia not meeting any other clinical criteria for severe disease	Country's specific cut-off for severe hypoxaemia will be used. All children recruited will be in the denominator.	At time of enrolment
Secondary	Proportion of children referred with hypoxaemia who receive oxygen at hospital	All children recruited will be in the denominator. Referral and hypoxaemia are assessed at Day0 consultation. Oxygen use at hospital is only available for hospitalised children from hospital records. At the time of enrolment hypoxaemia is measured and referral advise might be issued. Whether the child received oxygen or not at hospital is evaluated based on hospital registry and it refers to oxygen given at arrival to hospital. The specified time frame takes into account that the outcome is evaluated considering information recorded at different time points.	At time of enrolment and at time of hospitalization
Secondary	Proportion of children attending scheduled follow-up at the same facility by Day 7	All children recruited will be in the denominator.	From enrolment up to 7 days after
Secondary	Proportion of children presenting for unscheduled follow-up to any health facility by Day 7	All children recruited will be in the denominator.	From enrolment up to 7 days after