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.
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
- Conditions the study is for
- Vertical Human Immunodeficiency Virus Transmission, HIV Infection Pediatric, Infant Death
- 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
- Recruiting
Centro de Investigacao Operacional de Beira (CIOB), Instituto Nacional de Saúde (INS), Ministério da Saúde,
Beira
Joaquim Lequechane
Ilesh Jani, MD, PhD
Tanzania1 site, 1 recruiting
- Recruiting
National Institute for Medical Research (NIMR)
Mbeya, Mbeya
Issa Sabi, MD, PhD
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.
- Conditions
- Vertical Human Immunodeficiency Virus Transmission, HIV Infection Pediatric, Infant Death, Infant Morbidity, Infant, Newborn, Diseases
- 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 group | Role | What they receive |
|---|---|---|
| Cohort A | HIV-exposed infants and their mothers enrolled in the study Receives: Procedure: Maternal HIV viral load testing at delivery for VHT risk assessment | |
| Cohort B | HIV-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.
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)
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
Proportion and rate of VHT at birth, week 4-8, and week 14
Measured: 14 weeks
Risk-factors associated with VHT
Demographic, socio-economic, and behavioral data collected from mothers
Measured: 14 weeks
Adherence to PNP and ePNP
Measured: 14 weeks
Proportion and rate of clinical endpoints (mortality, morbidity) among HIV-positive infants at week 14, month 6, and month 12
Measured: 12 months
Age at ART initiation among HIV-positive infants
Measured: 12 months
Risk factors for poor ART adherence among high-risk mothers and infants
Measured: 12 months
Proportion of HIV-positive infants virally suppressed at week 14, month 6, and month 12
Measured: 12 months
Risk factors for poor viral suppression among HIV-positive infants
Measured: 12 months
Proportion of HIV-positive infants on ART that experience grade III or greater laboratory ART toxicity
Measured: 12 months
Retention to HIV EID and infant health care services
Measured: 14 weeks (Cohort A), 1 year (Cohort B)
Proportion of pregnant women presenting with criteria considered high-risk for VHT at delivery
Measured: 7 days
Proportion of mothers virally suppressed at week 14 post-partum
Measured: 14 weeks
Proportion and rate of post-partum mothers newly fulfilling high-risk criteria based on socio-behavioural criteria (i.e., adherence issues)
Measured: 14 weeks
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
Proportion of HIV-positive infants who develop acquired drug resistance mutations during the study
Measured: 12 months
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
Average public healthcare and healthcare-related expenditures
Measured: 12 months
Average health worker time needed to care for mothers and infants per clinic visit, including for enhanced counselling sessions
Measured: 12 months
Cost per HIV-exposed infant fulfilling the primary outcome
Measured: 12 months
Empirical cost-effectiveness (incremental cost-effectiveness ratio) relating intervention costs to life-years saved among HIV-positive infants
Measured: 12 months
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.
- First posted20 Feb 2024
- Study start30 Apr 2024
- Primary completionDec 2025 (estimated)
- Study completionDec 2025 (estimated)
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Other trials for Vertical Human Immunodeficiency Virus TransmissionStudies of the same condition, open and under way.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
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)
Sponsor and investigators
- Lead sponsor
- Michael Hoelscher
- Sponsor type
- University, hospital or other
- Collaborators
- National Institute for Medical Research (NIMR) - Mbeya Medical Research Centre (MMRC), Instituto Nacional de Saúde (INS), Ministério da Saúde, University of Liverpool
- Responsible party
- Sponsor-investigator, Michael Hoelscher, Ludwig-Maximilians - University of Munich
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