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RecruitingNCT06411405NeoRiskUpdated May 17, 2024

Using Machine Learning to Model Early-onset Neonatal Sepsis Risk in Uganda and Zimbabwe

An observational study in Neonatal Sepsis, sponsored by St George's, University of London. Recruiting at 2 sites in 2 countries. Open to female participants, including healthy volunteers. Per ClinicalTrials.gov, last updated 2024-05-17.

Sponsored by St George's, University of London · Observational

From the registry’s dates

  • Primary completion was expected by Dec 2024, 1 year 10 months ago, but the record still lists the study as recruiting.
  • Started Apr 2024; still recruiting 2 years 7 months later.
Study type
Observational
Model
Other
Time perspective
Prospective
Enrollment
2,500
Sex
Female
01

Study summary

The goal of this observational study is to develop a risk prediction model for early-onset neonatal sepsis in term and late preterm neonates in Uganda and Zimbabwe.

The main questions it aims to answer are:

  • What are the risk factors for early-onset neonatal sepsis in low-resource settings?
  • How can these be combined into a risk prediction model?

Mother-baby pairs will be recruited in Uganda. They will have extensive data taken on their medical and obstetric histories and lifestyles, and their newborns will have a blood sample taken just after birth for culture. Machine learning techniques will be used to create the risk prediction model, which will then be validated in a second population in Zimbabwe.

Read the detailed description

There will be three main phases to this study, which is an observational cohort study.

Phase 1 will take place at Kawempe Hospital in Kampala, Uganda. Participants will be recruited from labour wards by study staff, and interim analysis will be completed after recruitment of 10% of the total sample. See section 7.3 for further details.

Data will be collected via an online CRF, including the factors listed in the table in Section 3.

Additionally:

  • All neonates within the study will have a neonatal venous blood sample taken for culture by designated study staff

    o This must be taken before administration of antibiotics or within 48 hours of birth, whichever is sooner, and regardless of whether the neonate is being investigated and treated for sepsis.

  • Postnatal information will be collected via telephone at 1 month including maternal and infant outcome, hospital readmission or clinical illness, and vaccines given All data will be checked for quality control by a member of the study team. A blood culture will be taken from all neonatal participants at birth, prior to starting antibiotic treatment wherever safe to do so. The volume of blood taken for culture must be 1-2ml and will be verified by weighing blood culture bottles. Training will be provided to paediatric and study teams on blood culture sampling methods, including adequate cleaning of the skin prior to sampling. Feedback on sample volumes and contamination rates (see section 7.3 for definition) will be fed back to paediatric consultants, and additional staff training offered. Where sample is remaining after 3ml is added to the culture bottle, the excess will be retained as a blood spot sample for use in future ethically approved research, where the participant has consented to this.

The results of the microbiological tests will be communicated to the participant's clinical team in real time - see section 7.3.4 for further details. Clinician diagnosis of sepsis will be recorded where a clinician of registrar level or above has recorded a diagnosis of sepsis within 48 hours of birth. To reduce the subjectivity of this measure, GAIA level of certainty for a diagnosis of sepsis will also be assessed (35) and the level of diagnostic certainty recorded (1-5, as per GAIA criteria). Medical records are recorded on paper at Kawempe Hospital, before being coded into an electronic medical record by data clerks. PDF scans of medical records will be available where detailed review is required.

All participant data will be collected by trained study staff, and recorded into an online CRF hosted on REDCap, a secure web application. No patient identifiable data will be stored on the main REDCap database. See section 8.6 for further details of data management plans.

The postnatal information will be completed via a telephone call at 28 days post-delivery, made by study staff. Participants' contact number, a contact number for their partner, and a contact number for a second friend or family member will be taken at recruitment to minimise loss to follow up due to changes to mobile telephone number. Participant identity will be confirmed using three factors (date of birth, full name, address/village). The following information will be collected:

  • Health status of mother and baby
  • Any visits to medical care for the neonate

    • If attended or admitted to Kawempe hospitals, these electronic medical records will be reviewed by study staff
    • If attended elsewhere, the mother will be asked the reason for presenting, whether the neonate was admitted to hospital, the main diagnosis, and any treatments given.

Recruitment of the first 160 participants from labour ward (10% of the overall sample) will be treated as a pilot, and both recruitment and data will be reviewed at this point with particular attention to the following aspects:

  • Demographic comparison between recruited women and the population attending Kawempe
  • Data completion
  • Volume of blood culture samples taken
  • Loss to follow up rates
  • Association between potential risk factors and clinical sepsis, or culture-positive sepsis After this pilot analysis, the data collection instrument may be adjusted to be more concise if some risk factors appear to have no relationship with neonatal outcomes. Additionally, the recruitment strategy may be adjusted to include women attending antenatal clinics to improve the representativeness of the sample if the pilot sample is significantly different demographically to the general population of pregnant women attending the same study site antenatally. Finally, feedback and staff training will be given as needed to ensure optimal sample volumes and data completeness.

During Phase 1, two separate focus group discussions with 10 participants each will be held with staff from Kawempe Hospital. One discussion will be with senior clinicians, and one with junior clinicians and midwives. The focus groups will be held on site at Kawempe in English. Focus groups are being held in order to complement the quantitative results of this project by highlighting risk factors currently perceived as significant (which should then be a key part of analysis and results dissemination to confirm their usefulness), inform of current diagnostic difficulties to guide future work with the risk stratification model, and provide context for development and communication of the model to maximise its utility. The focus groups will address the following issues:

  • Ascertain knowledge and awareness of neonatal sepsis
  • Management of neonatal sepsis
  • regarding risks and consequences of neonatal sepsis, and
  • Current diagnostic strategies and their perceived strengths and difficulties
  • Perceptions of neonatal sepsis and how this might affect diagnosis and treatment
  • Recommendations to enhance the diagnosis and treatment of neonatal sepsis The focus groups will be conducted by members of MUJHU's social sciences team and Dr Sarah Sturrock. A tool has been developed by the social sciences team and Dr Sturrock for these discussions (see attached). The discussions will be recorded, and recordings destroyed once the discussions have been transcribed. The social sciences team will then complete thematic analysis of the discussions.

The investigators anticipate Phase 1 will take place between January and July 2024.

Phase 2 will use the data collected in phase 1 to construct a risk stratification model, in collaboration with the Advanced Research Computing Centre at University College London.

The investigators anticipate Phase 2 will take place between March and September 2024.

Phase 3 will involve external validation of the risk stratification tool. This phase will take place at Sally Mugabe Central Hospital in Harare, Zimbabwe. Participants will be recruited from antenatal clinics and labour wards by study staff.

Similar data will be collected from participants in Phase 3 as in Phase 1; following Phase 2, the data fields required for the model will be determined and these fields will be collected for Phase 3 participants.

Data collection will take place via the Neotree platform, which is in use at Sally Mugabe(41). Phase 1 will collect data on items not part of a standard medical history (such as sanitation availability and food security). Should any of these items form a key part of the statistical model, the possibility of adding these items to the Neotree platform will be discussed with the Neotree team. Pseudonymised data only will be extracted from the Neotree dataset, and the model from Phase 2 applied to determine the risk of neonatal sepsis.

The primary outcome for Phase 3 will be senior clinician diagnosis of sepsis recorded within 48 hours of delivery, and blood cultures (when available) will only be taken in neonates judged to be at risk of, or with clinical signs of sepsis as per standard clinical guidelines. Using senior clinician diagnosis of sepsis as the outcome is because supply of blood culture bottles and laboratory analysis of cultures is unreliable and is unlikely to be available to all study participants as in the Phase 1 setting.

Performance of the statistical model will be determined by calculating its sensitivity, specificity, positive and negative predictive values comparing calculated risk with clinical diagnosis of sepsis occurring within 72 hours of birth.

The investigators anticipate Phase 3 will take place between late 2024 and March 2025.

The TRIPOD (Transparent reporting of a multivariable prediction model for individual prognosis or diagnosis) statement have been followed in the design of this study and will be followed in its reporting(42). Adjustments will be made as necessary with the release of upcoming artificial intelligence-specific guidelines.

02

Conditions studied

  • Neonatal Sepsis

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03

In context

Neonatal Sepsis

192 studies on the registry are indexed under Neonatal Sepsis; 41 are open to participants now.

This study's planned enrollment of 2,500 is above the median of 200 across 85 observational studies indexed under Neonatal Sepsis.

Browse Neonatal Sepsis studies →

Lead sponsor

St George's, University of London is the lead sponsor of 106 studies on the registry; 12 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
Child (0–17), Adult (18–64), Older adult (65+)
Sexes eligible
Female
Accepts healthy volunteers
Yes
Sampling method
Non-probability sample

Study population

The study populations will be recruited from Kawempe National Referral Hospital in Kampala, Uganda and Sally Mugabe Central Hospital in Harare, Zimbabwe.

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

  • Neonates born at one of the study sites
  • Neonates born at ≥34 weeks gestational age, defined by:
  • Ultrasound scan, where participant has had an ultrasound scan during routine antenatal care
  • If no ultrasound scan has been done, according to last menstrual period date, according to mother
  • If no ultrasound scan has been done and the mother does not know her last menstrual period date, the neonate will be eligible for inclusion if their birth weight is ≥1400g which will include the majority of births ≥34 weeks according to the results of the INTERGROWTH-21st Project(44)

Exclusion criteria

Exclusion criteria

  • Neonates born at \<34 weeks gestational age, due to their higher background risk of sepsis, and automatic admission to the neonatal unit with antibiotic administration
  • Neonates with congenital abnormalities or syndromes associated with increased susceptibility to infection will be excluded (e.g. gastroschisis).
  • Neonates whose mothers are unable to provide
Terms in these criteria, in plain language(1)

Underlined terms in the criteria open these too. Explained by clinicaltrials.gg, not part of the registry record. The study team decides who can take part.

Informed consent

Before you join, the study team explains what taking part involves — its purpose, what happens, the risks and possible benefits — and answers your questions, so you can decide freely. Consent is usually recorded on a form (the informed consent form, ICF) signed by you or, where the law allows, by someone legally authorised to decide for you.

You can keep asking questions during the study, you are told of new information that matters, and you can choose to leave at any time.

05

Study design

Observational model
Other
Time perspective
Prospective
Enrollment
2,500 participants (estimated)
Patient registry
No
Biospecimen retention
Samples without dna

Groups and cohorts

  • Ugandan mother-baby cohort

    Mother-baby pairs recruited antenatally or at delivery, with babies eligible for inclusion if they are born at 34 weeks gestational age and above. Used as primary data for modelling.

    Other: Maternal medical history

  • Zimbabwean mother-baby cohort

    Mother-baby pairs with babies eligible for inclusion if they are born at 34 weeks gestational age and above, used as a validation cohort for the model.

    Other: Maternal medical history

Interventions

  • OtherMaternal medical history

    See above; multiple factors to be collected broadly grouped into maternal medical, obstetric, and sociodemographic/lifestyle factors.

    Also known as: Maternal obstetric/pregnancy history, Maternal sociodemographic/lifestyle factors

06

What researchers measure

Primary outcomes

  1. Positive blood culture amongst neonatal participants

    Venous blood culture processed on BACTEC machine

    Time frame: Sample taken in first 48 hours of life

Secondary outcomes

  1. Documented clinical diagnosis of sepsis amongst neonatal participants

    Diagnosis by specialist neonatal or paediatric doctor, documented in clinical notes or discharge letter

    Time frame: Within first 72 hours of life

  2. Clinical features of neonatal sepsis

    As defined by Brighton Collaboration GAIA criteria (https://doi.org/10.1016/j.vaccine.2016.03.046)

    Time frame: Within first 72 hours of life

  3. Admission to neonatal unit

    Admission to neonatal unit at study site or transfer to a neonatal unit at another facility

    Time frame: Within first 72 hours of life

  4. Readmission to hospital in first 28 days amongst neonatal participants

    Any readmission to any hospital

    Time frame: Within 28 days of birth

  5. Death before 28 days of age

    Maternal or other caregiver report of neonatal death

    Time frame: Within 28 days of birth

07

Study locations

1 of 2 sites recruiting
08

References and documents

Study documents

PDFs hosted by the registry, ClinicalTrials.gov.

Individual participant data

Plan to share: Undecided

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on May 17, 2024, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT06411405
Collaborators
MU-JHU CARE, Biomedical Research and Training Institute, Zimbabwe
Responsible party
Sponsor
First posted
May 13, 2024
Start date
Apr 11, 2024
Primary completion
Dec 31, 2024 (estimated)
Completion
Mar 1, 2025 (estimated)
Last update
May 17, 2024

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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