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Mixed-methods, descriptive and observational cohort study examining feeding and growth patterns among low birthweight infants in India, Malawi and Tanzania: the LIFE study protocol
  1. Linda Vesel1,
  2. Lauren Spigel1,
  3. Jnanindra Nath Behera2,
  4. Roopa M Bellad3,
  5. Leena Das2,
  6. Sangappa Dhaded3,
  7. Shivaprasad S Goudar3,
  8. Gowdar Guruprasad4,
  9. Sujata Misra2,
  10. Sanghamitra Panda5,
  11. Latha G Shamanur6,
  12. Sunil S Vernekar3,
  13. Irving F Hoffman7,
  14. Tisungane Mvalo8,9,
  15. Melda Phiri8,
  16. Friday Saidi8,
  17. Rodrick Kisenge10,
  18. Karim Manji10,
  19. Nahya Salim10,
  20. Sarah Somji10,
  21. Christopher R Sudfeld11,
  22. Linda Adair12,
  23. Bethany A Caruso13,
  24. Christopher Duggan14,
  25. Kiersten Israel-Ballard15,
  26. Anne CC Lee16,
  27. Stephanie L Martin12,
  28. Kimberly L Mansen15,
  29. Krysten North16,
  30. Melissa Young13,
  31. Emily Benotti1,
  32. Megan Marx Delaney1,
  33. Eliza Fishman1,
  34. Katelyn Fleming1,
  35. Natalie Henrich1,
  36. Kate Miller1,
  37. Laura Subramanian1,
  38. Danielle E Tuller1,
  39. Katherine EA Semrau1,17
  1. 1Ariadne Labs, Harvard T.H. Chan School of Public Health / Brigham and Women's Hospital, Boston, Massachusetts, USA
  2. 2Department of Paediatrics, SCB Medical College and Hospital, Cuttack, Orissa, India
  3. 3Jawaharlal Nehru Medical College, KLE Academy of Higher Education and Research, Belgaum, Karnataka, India
  4. 4Department of Neonatology, JJM Medical College, Davangere, Karnataka, India
  5. 5Department of Obstetrics and Gynaecology, City Hospital, Cuttack, Orissa, India
  6. 6Department of Paediatrics, SS Institute of Medical Sciences and Research Center, Davangere, Karnataka, India
  7. 7Institute for Global Health and Infectious Diseases, University of North Carolina at Chapel Hill School of Medicine, Chapel Hill, North Carolina, USA
  8. 8Department of Pediatrics, University of North Carolina Project Malawi, Lilongwe, Malawi
  9. 9Department of Pediatrics, University of North Carolina at Chapel Hill School of Medicine, Chapel Hill, North Carolina, USA
  10. 10Department of Pediatrics and Child Health, Muhimbili University of Health and Allied Sciences, Dar es Salaam, Tanzania
  11. 11Department of Global Health and Population, Harvard T.H. Chan School of Public Health, Boston, Massachusetts, USA
  12. 12Department of Nutrition, University of North Carolina at Chapel Hill Gillings School of Global Public Health, Chapel Hill, North Carolina, USA
  13. 13Hubert Department of Global Health, Emory University School of Public Health, Atlanta, Georgia, USA
  14. 14Center for Nutrition, Boston Children's Hospital, Boston, Massachusetts, USA
  15. 15Maternal, Newborn, Child Health and Nutrition Program, PATH, Seattle, Washington, USA
  16. 16Department of Pediatric Newborn Medicine, Brigham and Women's Hospital, Boston, Massachusetts, USA
  17. 17Department of Medicine, Harvard Medical School, Boston, Massachusetts, USA
  1. Correspondence to Dr Linda Vesel; lvesel{at}ariadnelabs.org

Abstract

Introduction Ending preventable deaths of newborns and children under 5 will not be possible without evidence-based strategies addressing the health and care of low birthweight (LBW, <2.5 kg) infants. The majority of LBW infants are born in low- and middle-income countries (LMICs) and account for more than 60%–80% of newborn deaths. Feeding promotion tailored to meet the nutritional needs of LBW infants in LMICs may serve a crucial role in curbing newborn mortality rates and promoting growth. The Low Birthweight Infant Feeding Exploration (LIFE) study aims to establish foundational knowledge regarding optimal feeding options for LBW infants in low-resource settings throughout infancy.

Methods and analysis LIFE is a formative, multisite, observational cohort study involving 12 study facilities in India, Malawi and Tanzania, and using a convergent parallel, mixed-methods design. We assess feeding patterns, growth indicators, morbidity, mortality, child development and health system inputs that facilitate or hinder care and survival of LBW infants.

Ethics and dissemination This study was approved by 11 ethics committees in India, Malawi, Tanzania and the USA. The results will be disseminated through peer-reviewed publications and presentations targeting the global and local research, clinical, programme implementation and policy communities.

Trial registration numbers NCT04002908 and CTRI/2019/02/017475.

  • epidemiology
  • neonatology
  • nutrition & dietetics
  • public health
  • qualitative research
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Strengths and limitations of this study

  • Our convergent parallel, mixed-methods study design will yield detailed and unique data on supply and demand side aspects of infant care, feeding and growth at the facility and community levels throughout the first year of life.

  • The LIFE (Low Birthweight Infant Feeding Exploration) study focuses on low birthweight (LBW) infants with birth weights between 1.5 kg and <2.5 kg given limited data on this birthweight group.

  • The multisite approach enables the comparison of results within and across three countries in sub-Saharan Africa and South Asia, where the phenotypes of LBW infants may vary.

  • The main limitation of this study is that enrolment is facility-based, missing the population of small infants who are born outside the health facility or delay presentation for care within the health system.

Introduction

Challenge

Although improvements in child health and survival have been achieved in the past two decades, a significant decline in neonatal mortality is needed to attain Sustainable Development Goal 3.2 by 2030.1 Focusing attention on the most vulnerable small and sick newborns, namely those born low birthweight (LBW, <2.5 kg), can reduce risk and poor outcomes in the first days, weeks and months of life. LBW, resulting from preterm birth and/or intrauterine growth restriction, accounts for 14.6% of newborn births, but represents 60%–80% of newborn deaths.2 This burden is disproportionately concentrated in low- and middle-income countries (LMICs).2 For at least the last 5 years, prematurity has been the predominant cause of mortality for children under 5 years of age.3 The mortality risk among infants born preterm and small-for-gestational age is more than 15 times greater than those born term and appropriate-for-gestational age.2 4–7

Additionally, LBW infants face increased risks for morbidity, neurodevelopmental impairments and growth faltering as well as challenges related to breast feeding, particularly its initiation and exclusivity in early infancy.2 8–12 Inadequate and insufficient feeding contributes to poor growth outcomes, such as stunting, wasting and underweight, for which the risk among LBW infants is already increased.13 Without close monitoring of growth and guidance on optimal feeding, LBW infants may not appropriately catch up to their non-LBW peers.

Design, testing and implementation of interventions to optimise feeding, growth and development among LBW infants requires a rigorously investigated foundational understanding of current practices, standard of care, outcomes and resource availability in LMICs.14 Limited evidence exists, particularly in low-resource settings, on feeding patterns and initiation, the feeding ecosystem, policies for the care of LBW infants and supply and demand inputs related to various feeding modes.15–17 Generally, studies capturing evidence on optimal milk type and content for moderately LBW infants (1.5 kg to <2.5 kg) in low-resource settings are lacking, hindering the proper management of nutritionally at-risk newborns.18 The World Health Organization (WHO) feeding guidelines for LBW infants were published in 201119; however, most of the recommendations are based on low quality evidence; even so, the majority of available evidence was from high-income countries, and most data were limited to very LBW infants (<1.5 kg) even though the majority of LBW infants are born between 1.5 kg to <2.5 kg.12 20

Opportunity

Despite these gaps, a number of opportunities in recent years have propelled interest and investment in the care of LBW infants. In 2012, the World Health Assembly highlighted the need to prevent LBW by setting a goal of reducing LBW births by 30% by 2025 as part of a set of 6 nutrition targets comprising its comprehensive implementation plan on maternal, infant and young child nutrition.2 In 2017, 40 global health organisations issued an urgent call to action for more evidence to address the current state of feeding of sick and vulnerable infants.21 In the past 2 years, the WHO, the United Nations Children’s Fund (UNICEF) and the United States Agency for International Development released reports and guidelines focusing on the care of the small and sick newborn.22 With interest and investment galvanised, research is needed to develop evidence-based approaches and translate findings into action to ensure the most vulnerable infants can survive and thrive.

Study aims

The Low Birthweight Infant Feeding Exploration (LIFE) study aims to document current feeding practices and growth patterns among LBW infants in LMICs to inform potential feeding interventions. The formative, observational cohort study has four objectives to be assessed among LBW infants using a mixed-methods approach: (1) understand feeding practices and the standard of care underpinning them; (2) explore the beliefs, facilitators and barriers around the feeding of LBW infants; (3) define and document key longitudinal growth and health outcomes up to 12 months of age; and (4) examine the relationships between infant and maternal characteristics, feeding, growth and child development. Before embarking on the formative research, we will conduct extensive desk reviews to better understand the current LBW infant feeding literature and policies in place. The long-term goal of the LIFE study is to inform the design of a future LBW infant feeding and growth trial and, in turn, strengthen the evidence-base for global infant feeding guidelines.

Methods and analysis

Study design

This protocol was developed based on the Strengthening the Reporting of Observational Studies in Epidemiology guidelines, the Consolidated Criteria for Reporting Qualitative Research guidelines, as well as key principles of designing and conducting mixed-methods studies.23–25 LIFE is a formative, multisite, observational cohort study involving 12 study facilities and using a convergent parallel, mixed-methods design. Quantitative and qualitative data will be collected and analysed in parallel and then merged at the interpretation phase.25 A mixed-methods approach allows us to establish the comprehensive foundational knowledge to design feeding interventions for nutritionally at-risk LBW infants. The purpose of the quantitative observational descriptive component of the LIFE study (including a retrospective chart review, prospective observational cohort, in-facility observational cohort and facility needs assessments) is to evaluate feeding practices and health outcomes among LBW infants and the health system inputs that support their care. The purpose of the qualitative descriptive component (including in-depth interviews (IDIs) and focus group discussions (FGDs)) is to examine the care and feeding of LBW infants from the perspectives of various key stakeholders. Finally, the integration of the quantitative and qualitative findings will allow us to more fully understand the context and reasons for the feeding patterns and health outcomes that we observe. Further details of the study design, objectives and data collection activities can be found in table 1. Data collection began in August 2019 and is on-going with plans for completion by October 2021.

Table 1

Details of study design, data collection and analysis

Study setting

The LIFE study is implemented in four sites across three countries: (1) Karnataka state, India and (2) Odisha state, India, led by teams at Jawaharlal Nehru Medical College, JJM Medical College, SS Institute of Medical Sciences, City Hospital and Srirama Chandra Bhanja Medical College; (3) Lilongwe, Malawi, led by the team at University of North Carolina (UNC) Project Malawi; and (4) Dar es Salaam, Tanzania, led by the team at Muhimbili University of Health and Allied Sciences. All sites have strong, long-standing relationships with key government stakeholders, placing them in a position to address local and national priorities and advocate for translation of research to practice. Sites were chosen in South Asia and sub-Saharan Africa as these regions represent the greatest burden of LBW as well as the diverse drivers of LBW.2 Investigators will document regional similarities and differences in maternal and infant characteristics, gestational age, birthweight, feeding patterns and growth. In total, participants are recruited from 12 study facilities (ie, secondary and tertiary hospitals) chosen based on delivery volume, capacity to care for LBW infants in the first days of life and willingness of facility leadership to participate. All facilities are located in urban settings with participants residing within a 50 km radius. Additional site details are included in table 2.

Table 2

Site descriptions

Study population

Quantitative

For the quantitative data collection activities, the study population comprises mother–infant pairs that include newborns with recorded birth weights of 1.5 kg to <2.5 kg, as well as health facilities (table 3). All 12 study facilities will participate in the facility needs assessments, including a facility profile and a donor human milk (DHM) bank assessment; further inclusion and exclusion criteria have not been specified.

Table 3

Inclusion and exclusion criteria for mothers–infant pairs

Qualitative

For the qualitative data collection activities, the study population includes mothers, family members (eg, husbands, guardians, mothers’ parents, mother’s in-laws, grandmothers, sisters and sisters-in-law), religious and community leaders, traditional healers, clinicians, government officials, supply chain experts and DHM banking experts meeting specific inclusion criteria (table 3). Mothers and family members of newborns with recorded birth weights of 1.5 kg to <2.5 kg are eligible for the IDIs and FGDs. Clinicians who have been at their position for less than 6 months are not eligible.

Patient and public involvement

As part of the study design, the LIFE team involves clinicians, researchers and community stakeholders familiar with the respective settings and populations. Study tools were piloted with patients and community members to ensure that research questions and indicators are culturally appropriate, acceptable and relevant to the study population.

Study measures

Quantitative

We evaluate key maternal and infant characteristics (eg, maternal education, maternal age, place of residence, parity, place and type of delivery, gestational age, infant sex and average length of facility stay) to better understand the LBW population in each site and region and to evaluate which characteristics serve as predictors of particular feeding patterns and growth and health outcomes. We examine infant feeding patterns including: early initiation of breast feeding (within 1 hour of birth), feeding profiles (exclusive breastmilk, mixed milk feeding or no breastmilk) at each visit week from birth to 12 months and duration of exclusive breast feeding (feeding of only breastmilk directly from the breast, expressed or from a donor). We will assess infant growth by measuring weight, length, head circumference and mid-upper arm circumference (MUAC) at 13 time points. Anthropometrics will be used to identify stunting (length-for-age z-score <-2SD), wasting (weight-for-length z-score <-2SD) and underweight (weight-for-age z-score <-2SD) at 6 and 12 months; and plot growth trajectories and velocities. Z-scores are derived from the International Fetal and Newborn Growth Consortium for the 21st Century (INTERGROWTH-21st) newborn size at birth and preterm postnatal growth standards26 27 and the WHO infant growth standards28 from birth through 12 months. We also examine weeks to birthweight regain, namely lack of regain in the first 2 weeks29–31; and identify infants experiencing slow weight gain (<20 g/day) in the second week of life (infants are meant to gain an average of 20 g/day in the first month of life and the second week of life is when infants should be gaining back their postnatal weight loss).32 33 The WHO standards were designed using a cohort of term infants while the INTERGROWTH-21st standards were designed specifically for preterm infants and serve as a complement to the WHO standards in the first 6 months of life. Additional health outcomes include infant morbidity based on maternal self-report of illnesses and symptoms experienced by the infants in the past week at each study visit; neonatal and infant mortality at any point during follow-up; and child development assessed via the Caregiver Reported Early Childhood Development Instruments at 1 year of age.34 Maternal study measures including illness, depression (based on the Patient Health Questionnaire-2) and anthropometrics (weight, height and MUAC taken when the infant was born, 6 weeks, 6 months and 12 months) are collected to evaluate mothers’ roles in the feeding and growth of their infants.35 Finally, data on bed capacity, length of stay post-delivery, neonatal intensive care admissions, infrastructure, space, equipment, feeding options, medications, staffing, service availability and sanitation practices are gathered to assess the health facility inputs available for care provision of LBW infants.

Qualitative

We explore beliefs, barriers, facilitators, risks and benefits of various feeding practices through structured IDIs and FGDs.

Data collection

Quantitative and qualitative data collection occur in parallel through 6 descriptive study activities (table 1). For most data collection activities, timing of data collection will be linked with infant age (figure 1). All data collection is prospective except for the chart reviews. Facility needs assessments are not included in figure 1 since they will not be linked to infant age; facility profiles are completed at baseline and DHM assessments over the course of the study.

Figure 1

Data collection timeline by activity and infant age.

Quantitative

Quantitative data collection is conducted by trained research nurses. The use of multiple data collection activities, combining observations and maternal self-report, helps to reduce bias and allows for triangulation of data. Retrospective patient chart data was collected for infants born in 12 study facilities between July 2018 and October 2019 using a structured survey. Chart reviews were completed before the initiation of prospective observational cohort data collection. The goal for the prospective cohort is to include 300 mother–infant pairs per site during 13 study visits using structured survey tools for infants born between September 2019 and January 2020 (noting that sites will start and end at different times) and completing 1-year follow-up in July 2021 (figure 1). Data are collected in-person at all time points, apart from at 32.5 and 45.5 weeks, at which time an abbreviated survey is administered over the phone in Malawi and Tanzania to bridge the 3-month time gap between in-person visits in order to reduce loss to follow-up; sites in India have previous experience with at least 3-month intervals between visits without adverse consequences on follow-up rates. Changes made in response to the COVID-19 pandemic included the addition of COVID-19 symptom screening questions, pauses to enrolment, data collection via phone calls where in-person visits were not possible and widening of the 6 month visit window. Table 4 summarises the assessments and timing of administration for the prospective observational cohort. Focused training was conducted by a paediatrician or research investigator for all assessments listed. Although this is an observational cohort study with no intervention, adverse events are monitored and recorded. The in-facility observational cohort is intended to include 35 mother–infant pairs per site from all participating study facilities via regular feeding observations (15 min each) and maternal reports starting within 6 hours of birth and continuing until facility discharge (first week—every 3–4 hours; second week—one to two times a day; and third week and thereafter—one time a day for unstable infants and every 3 days for stable infants) (table 4). Finally, facility needs assessment data are collected via standardised tools capturing key vital statistics; the structural, human resource, equipment and service inputs present for new mothers and newborns; and facility and programmatic readiness for establishing and strengthening DHM banks.29–32 Study team members administer the assessments at each of the study facilities through observations, record reviews and staff consultations; global DHM experts will participate in and provide detailed guidance for the DHM component.

Table 4

Timing of assessments for longitudinal prospective observational cohort

All sample sizes were determined to account for timeline, feasibility and resource constraints. Apart from the prospective observational cohort, we will not aim to make statistical inferences or precise point estimates from these samples, but will use the data descriptively for each infant to construct a narrative of their feeding patterns and health outcomes. The main statistical results from the prospective observational cohort will be point estimates and CIs for certain rates, such as the per cent of LBW infants who fail to thrive or whose growth falters, develop problems breast feeding or fall ill. The size of the true proportions will determine the precision of the estimate (eg, with a sample of 300 mother–infant pairs at each site, a true proportion of 10% can be detected with precision of ±3.6%). The 95% CI would be 6.4% to 13.6% (figure 2).

Figure 2

Margin of error in estimation of a single proportion with a sample of 300 at each study site for the prospective observational cohort.

To ensure standardisation and facilitate high quality data collection, investigators will conduct site-specific workshops to review tools and train research staff on how to prepare for and conduct all key assessments; timing and duration will be tailored to the needs and knowledge of each team. Supervisors perform regular quality checks and refresher training as needed. Standardised anthropometric equipment includes: Seca 334 mobile digital baby scale, 887/876/874 digital flat scale with foot pedal for maternal weight, site-specific height boards for mothers, Seca 417 infant measuring board, Shorr MUAC tapes for infants and mothers (WM-MUAC26) and Shorr 65 cm head circumference tapes for infants (SKU: WM-S Tape). The survey tools are administered in the local language (Hindi, Kannada and Marathi in India—Karnataka; Hindi and Oriya in India—Odisha; Chichewa in Malawi; and Swahili in Tanzania).

Qualitative

IDIs and FGDs with mothers and family members of LBW infants, community members, clinicians, government officials and supply chain and DHM knowledge experts took place between July 2019 and January 2021. All participants will only be interviewed once. Interviewers include men and women with clinical and/or research backgrounds including specialised training in qualitative data collection methods. They conduct IDIs and FGDs with stakeholders and clinicians in English, and with mothers, family members and community leaders in relevant local languages. Interviewers are not personally known to interviewees and are trained to reduce bias by building rapport with all participants and maintaining neutrality and confidentiality. They start each IDI and FGD by sharing the purpose of the study and any potential risks, obtaining consent and then use structured interview guides with specific probes; guides were piloted prior to data collection. All IDIs and FDGs are audio-recorded with permission from participants and supported with real-time note-taking; transcripts and/or summary notes will not be reviewed by participants. IDIs are scheduled for 1 hour and FGDs for 2 hours. All qualitative data collection takes place in a private location either within a study health facility or in the community setting. Participants are given a small incentive to participate in order to cover the cost of travel and lost wages.

We use purposive sampling for government officials and knowledge experts and convenience sampling based on availability for clinicians, mothers, family members and community leaders. Participants are approached in person or via email and visits are confirmed over the phone. Mothers of LBW infants aged 0–3 months and 4–7 months are sampled from facility patient charts while those aged 9 and 12 months are sampled from the prospective observational cohort based on their sex and presence or absence of stunting at 6 months of age. Our sampling strategy is designed to reach code saturation rather than meaning saturation.36

Data management and analysis

Quantitative

Quantitative data are entered and managed in CommCare,37 a secure electronic data capture and management system (retrospective chart reviews and prospective observational cohorts) and Microsoft Excel 2018, version 16.16.27 (facility needs assessments). For the prospective observational cohort only, the Tanzania team uses its own electronic data capture system and securely transfers data to be merged with the rest of the data collected in CommCare. All data used for analysis are de-identified and stored securely. Experienced statistical analysts and epidemiologists will use means, medians and SD to describe continuous variables and frequencies and proportions for categorical variables (all activities). For the prospective observational cohort, t-tests, χ2 tests and regression models (linear, logistic, log-binomial and/or poisson) will be used to explore relationships between key maternal and infant characteristics, feeding and growth. CIs around all measures will be constructed to adjust by site and cluster by mother to account for multiple births. Analyses will be stratified by site, sex and LBW phenotype. Missing data will be accounted for and denominators will be adjusted accordingly. Outliers for z-scores and anthropometrics will be examined and cleaned with the use of existing guidelines and sensitivity analyses, where helpful. Any further analyses will be post hoc and described separately. Analyses will be conducted using the Stata Statistical Software Package, V.1638 and the SAS statistical software suite.39

Qualitative

De-identified qualitative data are stored for internal use in SharePoint, a secure web-based document management and storage system. A codebook will be developed deductively (based on the research aims and interview guide questions to inform high-level codes) and inductively (based on the emerging content of the IDIs and FGDs to inform subcoded and emerging high-level codes) and applied to IDI and FGD data. Coding of the IDIs and FGDs will be performed by a total of seven coders and will involve a combination of rapid (framework analysis based on real-time notes supported by audio-recordings, where needed) and in-depth (coding of verbatim translated transcripts) approaches.40–42 Interviewers/site-based coders will employ a framework analysis and code notes into summary tables followed by subsequent coding (using a codebook) in Dedoose by qualitative researchers at Harvard. The first stage of data collection and coding in India and Malawi will be used to enable ongoing learning during the data collection process for a large volume of qualitative data.39 For maternal IDIs conducted among those with infants ages 9 months and older in India and Malawi, as well as all of Tanzania’s IDIs and FGDs across the full year of infancy, interviewers will transcribe the audio-recordings verbatim in English and the qualitative researchers at Harvard will conduct a comprehensive, thematic analysis of the data to identify key messages as well as similarities and differences across sites. During the analysis, researchers at Harvard will review all coded data and will identify, via Dedoose, themes that were most and least commonly mentioned. Themes will be further defined and discussed with the site-based coders to review the interpretation of the data and reduce bias. Data will be analysed by participant type and study location, and emergent key themes will be used to inform recommendations for future interventions.

Protocol and registration

The study is registered with ClinicalTrials.gov and Clinical Trial Registry of India (http://ctri.nic.in).

Ethics and dissemination

This study was approved by 11 ethics committees in India, Malawi, Tanzania and the USA: (1) India Health Ministry’s Screening Committee with Indian Council of Medical Research acting as its secretariat (2019–2674); (2) Directorate of Health and Family Welfare Services, Government of Karnataka, which also covers investigators at Women and Children Hospital, Davangere and Chigateri General District Hospital, Davangere (NHM/SPM/04/2019–20); (3) Institutional Ethics Committee of KLE Academy of Higher Education and Research which also covers investigators at JN Medical College, Belagavi and KLES Dr Prabhakar Kore Hospital & Medical Research Center, Belagavi (KAHER/IEC/2019–20/D-2760); (4) Institutional Ethics Review Board of SS Institute of Medical Sciences and Research Centre (IERB/200/2019); (5) Institutional Ethics Committee of JJM Medical College (JJMMC/IEC-01/2019), which also covers investigators at Bapuji Child Health Institute and Research Centre, Davangere, Women and Children Hospital, Davangere and Chigateri General District Hospital, Davangere; (6) Research and Ethics Committee, Directorate of Health Services, Odisha state, which also covers investigators at City Hospital Oriya Bazar, Cuttack (155/PMU/187/17); (7) Institutional Ethical Committee, Sriram Chandra Bhanja Medical College, Cuttack (7188); (8) Malawi National Health Sciences Research Committee (NHSRC2019/Protocol19/03/2250-UNCPM 21905); (9) Tanzania National Institute of Medical Research (NIMR/HQ/R.8a/Vol.IX/3126); (10) Muhimbili University of Health and Allied Sciences (DA.282/298/01.C/); and (11) Harvard T.H Chan School of Public Health (IRB10-0282) which also covers investigators at Boston Children’s Hospital, Brigham and Women’s Hospital, Emory University, PATH and University of North Carolina.

Written informed consent is obtained from all IDI, FGD, in-facility observational cohort and prospective observational cohort participants. After 6 months of follow-up, prospective observational cohort participants will be re-consented for an additional 6 months. Verbal consent will only be obtained in the event of extenuating circumstances where written consent cannot be sought; Institutional Review Board approval will be needed before proceeding. For the facility needs assessments, verbal consent is sought at the facility leadership level as these activities are considered to be a part of quality improvement. Results from the LIFE study will be disseminated at global-levels and site-levels through peer-reviewed publications and presentations to key stakeholders during meetings and conferences. Site investigators will also share results informally with participating study facilities. On publication of the study results, select data will be made publicly available via Harvard Dataverse.43

Discussion

The LIFE study will fill critical data gaps in the care and nutrition of LBW infants in LMICs; although limited, most of the existing research in this area is concentrated in high-income countries.18 Overall, evidence is lacking on feeding, care and health of LBW infants born with birth weights of 1.5 to <2.5 kg; however, these moderately LBW infants represent the majority (>90%) of global LBW births compared with very LBW infants (<1.5 kg).2 17 18 44–46 We will aim to establish the foundational knowledge required to design, test and implement the most effective and feasible infant feeding strategies to prevent and address growth faltering among LBW infants in low-resource settings. The LIFE study will provide the much-needed evidence to comprehensively understand what LBW infants require, how they differ from infants born ≥2.5 kg and what rigorous research is critical to strengthen global LBW infant feeding guidelines.

Ethics statements

Patient consent for publication

Acknowledgments

The authors would like to thank clinical leadership and staff at all study facilities for their partnership, support and contribution to this work; the mothers and infants for allowing us to have a glimpse into their experiences and sharing key moments of their lives; community members, government officials and subject experts for sharing their perspectives; and all data collectors and study staff for conducting study activities.

References

Footnotes

  • Twitter @DrFridaySaidi, @k_semrau

  • Contributors Study conceptualisation and design was completed by ACCL, BAC, CD, CRS, DET, EB, IFH, KEAS, KI-B, KLM, KMa, KMi, KN, LA, LSp, LSu, LV, MY, NH, RMB, SD, SSG and TM. Protocol development and tool design was carried out by ACCL, BAC, CRS, DET, EB, EF, GG, IFH, JNB, KEAS, KF, KI-B, KLM, KMa, KMi, KN, LA, LD, LGS, LSp, LSu, LV, MY, MMD, NH, NS, RK, RMB, SLM, SM, SP, SMD, SSG, SS, SSV and TM. Tool pilot testing/modification were conducted by EB, EF, FS, GG, JNB, KF, LD, LGS, LSp, LSu, LV, MP, NH, NS, SM, SP, SS and SSV. Writing of the manuscript was conducted by LSp and LV. All authors reviewed multiple drafts of the manuscript and approved the final version.

  • Funding This work was supported, in whole or in part, by the Bill & Melinda Gates Foundation [OPP1192260]. Under the grant conditions of the Foundation, a Creative Commons Attribution 4.0 Generic License has already been assigned to the manuscript. The Bill & Melinda Gates Foundation reviewed the study design and sample-size calculations, but will not be involved in data collection, management, analysis, interpretation, writing of the manuscript, or the decision to submit manuscripts for publication.

  • Competing interests All authors completed the ICMJE conflict of interest form and were funded by the Bill & Melinda Gates Foundation for this work as part of the LIFE study. ACCL, BAC, CRS, DET, KEAS, KI-B, KLM, KMa, MMD, RK and SS have received funding from the Bill & Melinda Gates Foundation for maternal and newborn health work at large. CD reports other from American Society for Nutrition, other from UpToDate and other from People’s Medical Publishing House outside the submitted work. ACCL reports grants from the WHO and National Institute of Health NICHD outside the submitted work.

  • Patient and public involvement Patients and/or the public were involved in the design, or conduct, or reporting, or dissemination plans of this research. Refer to the Methods section for further details.

  • Provenance and peer review Not commissioned; externally peer reviewed.