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Vertical Human Immunodeficiency Virus TransmissionLIFE2ScaleNCT06267508

Increasing Neonatal HIV Test and Treat to Maximize the Long-Term Impact on Infant Health and Novel Infant Antiretroviral Treatment

An observational study of Vertical Human Immunodeficiency Virus Transmission and HIV Infection Pediatric, run by Michael Hoelscher at 2 sites in 2 countries.

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Looking for participants now. Contact the study team or a site below to ask about taking part.

Sites and contacts
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Trial summary

This study aims to improve HIV healthcare services for mothers living with HIV and their newborns in Tanzania and Mozambique. The main questions it aims to answer are: 1) does enhancing screening with maternal HIV viral load monitoring at delivery identify more mother-child pairs at high-risk for HIV vertical… Read more about this study

Who is it for?
Ages 18 years and older, women only
What is being tested?
Maternal HIV viral load testing at delivery for VHT risk assessment
Type of treatment
Surgery or procedure
How many people
6,000 participants
Where
2 sitesin 2 countries
Study dates
30 Apr 2024to Dec 2025
Phase
Observational

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 18 years and older
  • Women only
  • No healthy volunteers
  • Adult, Older adult

Study population: Pregnant women living with HIV and their exposed infants recruited at maternity clinics in Mozambique and Tanzania. The investigators expect to recruit 4000-6000 mother-child pairs in 12 months, or 56-71 mother-child pairs per cluster-randomization period (7 weeks) into Cohort A. Assuming 12-week VHT rates of 2.5% and 1% VHT rates in Mozambique and Tanzania respectively, the investigators expect to roll-over approximately 105 HIV positive infants (75 in Mozambique and 30 in Tanzania) from both countries into Cohort B.

Who may be able to join

  • Voluntary and informed consent of the mother for her own study participation (if applicable);
  • Voluntary and informed consent of the legal guardian of the child for participation of the child in the study;
  • Mothers/legal guardians ≥18 years of age;
  • Documented maternal HIV infection;
  • Willingness to consent to HIV testing for the child and herself (or just her child); and
  • Willingness to consent to active tracing including home tracing.

Who cannot join

  • Deficiency in the mother, rendering it difficult, if not impossible, for her or her infant to take part in the study or understand the information provided to her.
  • Having delivered more than 72h (3 days) ago;
  • Prisoners;
  • Women presenting with an emergency requiring immediate medical assistance if not resolved at study inclusion;
  • Stillbirths;
  • Infant requiring emergency care (e.g. immediate or rapid occurring life threatening conditions, resuscitation, prolonged obstetric related intensive care, severe jaundice) or born with severe malformation;
  • If within the discretion of the investigator based on recommendation of the gynaecologist or paediatrician in charge study participation would possibly add not acceptable risk or burden to the mother or infant (e.g. significant congenital malformation, health deficiencies, very low birth weight less than 1500g); or
  • Unlikely to comply with protocol as judged by the principal investigator or his designate

Trial locations and contacts

2 sites in 2 countries. Contact the study team or a site near you to ask about taking part.

Amy Heilman contact

2 sites in 2 countries

Mozambique1 site, 1 recruiting
  • Centro de Investigacao Operacional de Beira (CIOB), Instituto Nacional de Saúde (INS), Ministério da Saúde,

    Beira

    Joaquim Lequechane

    Ilesh Jani, MD, PhD

    Recruiting

Other trials in Mozambique

Tanzania1 site, 1 recruiting
  • National Institute for Medical Research (NIMR)

    Mbeya, Mbeya

    Issa Sabi, MD, PhD

    Recruiting

Other trials in Tanzania

About this study

This study aims to improve HIV healthcare services for mothers living with HIV and their newborns in Tanzania and Mozambique. The main questions it aims to answer are: 1) does enhancing screening with maternal HIV viral load monitoring at delivery identify more mother-child pairs at high-risk for HIV vertical transmission? and 2) are high-risk infants linked to appropriate prevention and care? The study will expand access to HIV testing services to more rural settings using a hub-and-spoke referral system.

Read the detailed description

The UN Sustainable Development Goals set the ambitious goal to eliminate new paediatric HIV infections by 2030. Between 2010 and 2020, new HIV infections among children declined by more than 50%. This decline demonstrates the goal is achievable, but the loss of momentum in recent years indicates a need for further improvements. Results from the previous LIFE study conducted in Mozambique and Tanzania demonstrated that identifying HIV-infection in neonates and starting HIV treatment as early as birth is feasible and may reduce infant death and severe disease. However, this study also demonstrated that it is difficult to administer infant HIV treatments due to poor palatability of the infant drug formulation, socio-behavioural constraints for mothers, and care linkage challenges. This resulted in poor treatment adherence and efficacy (as measured by HIV suppression rates in the blood).

The investigators propose to expand and optimize treatment and prevention interventions for mothers living with HIV and their newborns and translate previous research findings into policy and practice, with a focus on primary healthcare to reduce access inequities in rural areas. The study aims to scale-up of tools used for vertical HIV transmission risk screening affiliated with immediate, risk-based HIV test \& treat procedures. Testing for high-risk case detection will be implemented in a hub-and-spoke model, where smaller, less well-equipped health facilities refer samples to nearby larger health facilities for diagnostic testing, ensuring rural communities have access to the interventions. The investigators will also provide personnel support for scale-up of high-risk case detection and high-risk infant care management. Furthermore, all high-risk mother-baby pairs will receive enhanced counselling services. eHealth tools for electronic result sharing across health facilities will be part of our package of interventions.

The investigators will evaluate the impact of the intervention package described above on key prevention of vertical HIV transmission (PVHT) program indicators (e.g., percentage of high-risk newborns immediately tested for HIV, percentage of newborns with HIV immediately started on treatment) in a stepped-wedge, cluster-randomized study. The investigators will also conduct a cost-effectiveness analysis of the intervention package. Furthermore, the investigators will conduct interviews and use self-reported questionnaires by the participants and site staff to better understand the socio-economic and behavioural factors contributing to high-risk classification.

For HIV-positive babies, the investigators will assess the impact of a novel HIV drug used for newborns, i.e. Dolutegravir (DTG), on health outcomes. The investigators will also characterize the impact of transmitted and acquired genotypic drug resistance, as well as transmitted viral strains, towards neutralization against established and novel broadly neutralizing antibodies. This information will be used to inform future prevention and treatment strategies for HIV-exposed newborns.

All mothers of HIV-positive babies taking part in this study will continue to have access to enhanced counselling and care support throughout the study, and the investigators will collect information on socio-behavioural factors influencing treatment outcomes to understand challenges related to infant HIV treatment.

This study will be performed by an established consortium of interdisciplinary African and European experts, closely collaborating with health authorities and policy makers, thus ensuring effective and sustainable implementation, programmatic stewardship, and global access to the proposed complex intervention.

Being tested
Maternal HIV viral load testing at delivery for VHT risk assessment
Keywords
Prevention of Vertical HIV Transmission (PVHT), Infant HIV Prophylaxis, Early Infant HIV Diagnosis, Infant Antiretroviral Treatment
Medical subject headings
Infant Death, Infant, Newborn, Diseases

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • Maternal HIV viral load testing at delivery for VHT risk assessmentProcedure or surgery

    Maternal HIV viral load testing will be performed for all mothers enrolled in the study at delivery. Results will be used along with WHO-defined clinical criteria to determine risk status for VHT. The intervention also includes personnel to support the additional testing volume and management of high-risk cases and eHealth solutions for communication of test results between health facilities.

Study groups in NCT06267508
Study groupRoleWhat they receive
Cohort AHIV-exposed infants and their mothers enrolled in the study
Receives: Procedure: Maternal HIV viral load testing at delivery for VHT risk assessment
Cohort BHIV-positive infants, identified in the first 12 weeks, and their mothers will be rolled over from Cohort A to Cohort B for long-term follow-up for up to 12 months.

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Proportion of HIV-exposed infants correctly identified as low- or high-risk and receiving birth EID testing and ePNP or ART as appropriate within 7 days of life

    All infants enrolled in the study: 1) assessed for high-risk criteria for VHT at birth, 2) if high-risk, receiving enhanced post-natal prophylaxis (ePNP) and PoC birth EID testing, AND 3) if HIV-positive, initiated on ART

    Measured: 7 days

Secondary outcomes (22)
  1. Turnaround times for EID testing at birth, 4-6 weeks, and 14 weeks (time from sample collection to receipt of results by the health facility and communication of results to the mother/caregiver) and maternal PoC VL testing at delivery and 14 weeks

    Measured: 14 weeks

  2. Proportion and rate of VHT at birth, week 4-8, and week 14

    Measured: 14 weeks

  3. Risk-factors associated with VHT

    Demographic, socio-economic, and behavioral data collected from mothers

    Measured: 14 weeks

  4. Adherence to PNP and ePNP

    Measured: 14 weeks

  5. Proportion and rate of clinical endpoints (mortality, morbidity) among HIV-positive infants at week 14, month 6, and month 12

    Measured: 12 months

  6. Age at ART initiation among HIV-positive infants

    Measured: 12 months

  7. Risk factors for poor ART adherence among high-risk mothers and infants

    Measured: 12 months

  8. Proportion of HIV-positive infants virally suppressed at week 14, month 6, and month 12

    Measured: 12 months

  9. Risk factors for poor viral suppression among HIV-positive infants

    Measured: 12 months

  10. Proportion of HIV-positive infants on ART that experience grade III or greater laboratory ART toxicity

    Measured: 12 months

  11. Retention to HIV EID and infant health care services

    Measured: 14 weeks (Cohort A), 1 year (Cohort B)

  12. Proportion of pregnant women presenting with criteria considered high-risk for VHT at delivery

    Measured: 7 days

  13. Proportion of mothers virally suppressed at week 14 post-partum

    Measured: 14 weeks

  14. Proportion and rate of post-partum mothers newly fulfilling high-risk criteria based on socio-behavioural criteria (i.e., adherence issues)

    Measured: 14 weeks

  15. Characteristics of transmitted viral strains (lineages, subtypes, resistance mutations) among HIV-positive infants and in comparison to their mothers viral sequences

    Mother-child comparative genomic analysis and virus quasi-species diversity (major/minor and transmitted strains)

    Measured: 12 months

  16. Proportion of HIV-positive infants who develop acquired drug resistance mutations during the study

    Measured: 12 months

  17. Characteristics of infant and maternal HIV strains to be neutralized against a panel of known broadly neutralizing antibody candidates (e.g., VRC07, 10-1074) and maternal autologous antibodies at time of transmission

    Measured: 12 months

  18. Average public healthcare and healthcare-related expenditures

    Measured: 12 months

  19. Average health worker time needed to care for mothers and infants per clinic visit, including for enhanced counselling sessions

    Measured: 12 months

  20. Cost per HIV-exposed infant fulfilling the primary outcome

    Measured: 12 months

  21. Empirical cost-effectiveness (incremental cost-effectiveness ratio) relating intervention costs to life-years saved among HIV-positive infants

    Measured: 12 months

  22. Average global and dimensional patient satisfaction

    Measured: 14 weeks

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted20 Feb 2024
  2. Study start30 Apr 2024
  3. Primary completionDec 2025 (estimated)
  4. Study completionDec 2025 (estimated)

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Observational
Observational model
Cohort
Time perspective
Prospective
Enrolment
6,000 participants (estimated)
IDs, dates and publications
ClinicalTrials.gov ID
NCT06267508
Sponsor's protocol ID
LMU-IMPH-LIFE2Scale
Acronym
LIFE2Scale
Status last verified
Nov 2024
First submitted
24 Jan 2024
Last updated
18 Nov 2024
Results posted
No
Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
No

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