Clinical Trials Logo

Clinical Trial Summary

Globally, 15% of all babies, amounting to 20 million infants each year, are born low birthweight (LBW), defined less than 2500 grams (5.5 lbs). Compared to normal weight infants, LBW infants are at higher risk of morbidity, mortality, and poor growth (Risnes et al 2011; Larroque et al 2001; WHO 2006). The main causes of LBW are preterm birth, intrauterine growth restriction (IUGR), or their combination. Unfortunately, there is a paucity of information around feeding practices and optimal feeding strategies for this population, particularly for LBW infants who struggle with breastfeeding or growth. This study hopes to address these gaps.


Clinical Trial Description

The Low-birthweight Infant Feeding Exploration (LIFE)(original grant 0-6 months of age) and the 6- month extension (6-12 months of age) will fill a critical data gap in the field of newborn care regarding vulnerability and feeding of LBW infants. The investigators aim to establish the background information required to set up and test the most efficient and feasible infant feeding strategies for LBW infants: first to support breastfeeding, and then to support infants who are nutritionally at risk in the first 6 month of life in low and middle income countries (LMIC). The investigators will explore all three infant feeding options currently included in the WHO guidelines for LBW infants (WHO 2011), namely mother's own milk (MOM), donor human milk (DHM), and breast milk substitute or formula (BMS), in that order. This work will provide much-needed evidence to inform infant feeding guidelines. In addition, this 6-month extension will allow for a more comprehensive exploration and understanding of feeding options for LBW infants from 6 to 12 months of age, accounting for timing of introduction of complementary liquids and foods, changes in feeding types, growth and health outcomes over the entire infancy period. This will contribute significantly and allow for high quality data to describe the burden of disease across sites. Specifically, we will be able to describe the following for LBW infants: - Growth trajectories from 0 to 12 months of age - Patterns and timing of complementary feeding and continued breastfeeding/breastmilk consumption - Common infant morbidities and timing of mortality - Maternal demographics, well-being and environmental factors affecting infant feeding and growth The overall study goal is to understand feeding options for LBW infants in LMIC settings, including current feeding practices, health outcomes, and potential interventions. The study will take place in four study sites located in three countries: Tanzania, Malawi, and India. Each study site will encompass 2 to 5 individual study facilities. The three study objectives under the goal include: 1. Understand the current practices and standard of care (SOC) for feeding LBW infants 2. Define and document the key outcomes (including growth, morbidity, and lack of success on MOM) for LBW infants under current practices 3. Assess the acceptability and feasibility of a system-level IYCF intervention and the proposed infant feeding options for LBW infants The investigators will also use the results of this work to design ways to support exclusive breastfeeding (including strategies for feeding with MOM), and to support other options, when mother's own milk (MOM) is unavailable or infants are nutritionally at risk. To do this, the investigators will engage in discussion and consensus-building activities among study staff and key stakeholders, using the collected study data to inform feasible, acceptable Infant and Young Child Feeding (IYCF) strategies for LBW infants that include specific options for those who are nutritionally at risk. The strategies will be tailored to the country as much as possible. A primary product for this later stage will be a white paper documenting key findings from the research and proposing feeding strategies for LBW infants in study sites. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT04002908
Study type Observational
Source Harvard School of Public Health (HSPH)
Contact
Status Completed
Phase
Start date July 31, 2019
Completion date July 29, 2021

See also
  Status Clinical Trial Phase
Completed NCT04200807 - Non-invasive Measurement of Neonatal Central and Peripheral Hemodynamics
Active, not recruiting NCT05282628 - I-InTERACT Preterm N/A
Recruiting NCT04717037 - Olive Oil Massage Effect for Reduction of Preterm Sepsis (OMEPS) Phase 2/Phase 3
Completed NCT05017727 - Closed-loop Oxygen Control in Ventilated Infants Born at or Near Term
Completed NCT04633551 - Vascular Inflammation and Anti-inflammatory Supplements After Adverse Pregnancy Outcomes N/A
Completed NCT04295395 - Evaluation of the Brain and Renal Regional Oxygenation Using NIRS in Preterm Infants
Recruiting NCT05383586 - MusicHyperBrain Study With Preterm Infants and Their Parents N/A
Not yet recruiting NCT04812249 - Effect of Co-morbidities on the Development of Oral Feeding Ability in Pre-term Infants
Recruiting NCT03966170 - Citicoline as Neuroprotector in Preterm Phase 3
Completed NCT05863481 - Obstetric Outcome in Pregnancies Treated With Laparoscopic Cerclage
Recruiting NCT05404594 - Multimodal Approach to the Ontogenesis of Nociception in Very Preterm and Term Infants N/A
Not yet recruiting NCT05188066 - Study of Pregnancy Pathologies Associated With Placental Abnormalities
Not yet recruiting NCT05629910 - NeO2Matic-Pilot Trial N/A
Completed NCT04811872 - Placental Transfusion Effect on Hemodynamics of Premature Newborns Phase 2/Phase 3
Completed NCT04785183 - Antioxidant Effects of Melatonin in Preterm N/A
Not yet recruiting NCT05243901 - EPIPAGE 2 - 10-year Follow-up (RECONAI PROJECT)
Not yet recruiting NCT04333121 - Modelling Weight Reference Centiles for Preterm Infants
Completed NCT04292015 - Optos Versus Indirect Ophthalmoscopy for ROP Screening Examination (Optos vs BIO Study) N/A
Not yet recruiting NCT04351425 - Early Weaning of Preterm Newborn From Incubator to Cot at 1400 Grams N/A
Not yet recruiting NCT06354517 - The Impact of the SENSE Program on NICU N/A