The Alberta BLOOM Premature Child Study
For patients and families
In plain language
An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.
- What is being studied
- This is an observational study: the protocol does not assign a study treatment.
- Who it may be relevant to
- Registry conditions: Infant Conditions, Infant, Premature, Diseases, Asthma, Asthma in Children. Basic parameters: from 0 Days · All.
- What needs checking
- Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
- Where it takes place
- Canada
- Next step
- Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
Unsure about the terms? Read our patient guide →
Official title
The Alberta BLOOM Premature Child Study: Impact of the Microbiome on the Clinical Course and Health Outcomes of Premature Children
Overview
This is a prospective, observational clinical cohort study involving 405 children born premature (at less than 37 weeks gestation) and their mother/parent/guardian. The purpose of the study is to investigate how the microbiome (the collection of microbes in a biological site) of children develops over the first years of life and its associations with the risk of childhood health outcomes including allergies and asthma. The study will also examine how perinatal factors associate with patterns of microbiome development, and their effects on the microbiome, metabolome (the collection of metabolites in a biological sample) and immune development of this population in the first years of life.
Detailed description
Premature birth (birth before 37 weeks of pregnancy) occurs in about 1 in 10 pregnancies. When infants are born prematurely their gut is not as developed. One important factor in gut health is the large community of microbes (tiny living things such as bacteria) that live on the human body called the microbiome. Recent studies have shown that premature infants are more likely to experience changes to their gut microbiome that are associated with health issues, such as asthma and allergies. However, the specific microbiome features of children born preterm and the role of their microbiome in disease risk and childhood health is not well understood. The Alberta BLOOM Premature Child Study (PCS) investigates how the microbiome and immune health of premature children develops over the first years of life and its associations with the risk of childhood health outcomes. BLOOM-PCS will also study how the microbiome of children born premature differs from the microbiome in the term population.
The type of microbes that are present in the infant's gut in the first months of life have a major impact on the microbiome that will form during childhood. There are many environmental factors during pregnancy, birth and the first months of life that can impact an infant's microbiome development. Factors such as diet, exposure to antibiotics, surgical procedures, and mode of delivery can strongly affect early microbiome development. This study will investigate how these factors influence the types of early microbes present in preterm infants.
This study hypothesizes that specific microbial patterns, trajectories and/or metabolites will be significantly associated with single or a combination of perinatal maternal and/on infant factors. Also, that microbial alterations resulting from preterm birth contributes to the allergy and asthma outcomes in infants through immune mechanisms.
Primary outcome measures
- Infant outcomes at 1 and 3 years of age [Time frame: 1-3.5 Years Corrected Gestational Age]
Secondary outcome measures (3)
- Microbiome [Time frame: 0-3.5 Years Corrected Gestational Age]
- Metabolome [Time frame: 0-3.5 Years Corrected Gestational Age]
- Perinatal factors and microbiome, metabolome and immunobiome [Time frame: 0-3.5 Years Corrected Gestational Age]
Eligibility criteria
Inclusion criteria
Child Inclusion Criteria:
- Less than 8 days of age or previous participation in one of the BLOOM-PTN, BLOOM-LTFU, Pregnancy During the Pandemic or PROBIO studies;
- Born at ≤ 36 weeks + 6 days gestation (36 6/7 weeks gestational age)
- For babies recruited shortly after birth, be expected to survive more than one week;
Mother/Parent/Legal Guardian Inclusion Criteria:
- Provide a signed and dated consent form;
- Be able to speak and understand English;
- Be 16 years of age or older;
- Be willing to comply with all study procedures and be available for the duration of the study;
- If recruited as a previous participant of the BLOOM-PTN, BLOOM-LTFU, Pregnancy During the Pandemic and/or PROBIO studies, must be willing to attend clinic visit(s) at the Alberta Children's Hospital in Calgary, Alberta at 1 and 3 years Corrected Gestational Age, or
- If recruited within 8 days of birth, must reside within the Calgary Metropolitan Region.
Exclusion criteria
Child Exclusion Criteria:
- Has major congenital or chromosomal anomalies, including any congenital gastrointestinal anomalies
- Children recruited within 8 days of birth who have a history of gastrointestinal surgery at the time of recruitment
Mother/Parent/Legal Guardian Exclusion Criteria:
- Not the legal guardian of the child or
- In a legal guardianship dispute.
Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.
Healthy volunteers: No
Study design
- Observational model
- Cohort
Study locations
Canada · 1 center
- University of Calgary — Calgary
Identifiers
NCT: NCT05011071 · REB20-1442