Actively Recruiting
Maternal Iron Deficiency and Childhood Health - a Prospective Cohort Study
Led by Tampere University Hospital · Updated on 2025-03-17
6000
Participants Needed
1
Research Sites
365 weeks
Total Duration
On this page
Sponsors
T
Tampere University Hospital
Lead Sponsor
T
Tampere University
Collaborating Sponsor
AI-Summary
What this Trial Is About
Researchers are studying how maternal iron deficiency and iron deficiency anemia, along with the use of iron supplements during pregnancy, affect the health and development of children up to seven years old. This prospective observational cohort study involves pregnant women who visit Tampere University Hospital for prenatal care or labor. The study also includes two smaller groups focusing on mothers with iron deficiency or diabetes to explore how maternal iron status relates to the child's iron levels and development. All pregnant women who agree to participate complete an online questionnaire about their anemia diagnosis, iron supplement use, chronic diseases, and any intravenous iron treatments during pregnancy. The mothers' iron status is tested before delivery, and their children's iron levels are checked at birth, a few days after birth, and again at 8 months, 2 years, and 5 years. Parents also fill out questionnaires about their child's nutrition, sleep, behavior, and development at these same ages. Participants' health records will be followed from birth until the child is seven years old to gather information on growth, diagnoses, medications, and support needs at school. Data collection began in April 2024 and will continue for about 3.5 years, with ongoing follow-up of children through outpatient records. The study aims to provide insights that could guide pregnancy care and future recommendations for diagnosing and treating iron deficiency in mothers and children.
CONDITIONS
Brief Title
Maternal Iron Deficiency and Childhood Health
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Pregnant
- Can read and write Finnish, Swedish or English
You will not qualify if you...
- Illiterate
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Your Study Journey
Duration - Up to 3.5 years during recruitment
Participants are screened for eligibility to participate in the trial.
Prenatal visits or hospital visits for labor
Duration - From pregnancy through delivery and up to 1 month of age for newborns
Participants' iron status and health data are collected from mothers and newborns through questionnaires, lab tests, and medical records.
1 visit for hemoglobin and iron status testing before delivery, cord blood and newborn tests at birth and 2-5 days of age
Duration - From birth until 7 years of age
The child's health and development are followed through medical records and questionnaires at multiple ages.
Questionnaires and lab tests at 8 months, 2 years, and 5 years; health record reviews at 1.5, 4, and 7 years
Trial Site Locations
Total: 1 location
1
Tampere University Hospital
Tampere, Pirkanmaa, Finland, 33520
Actively Recruiting
Research Team
L
Laura K Seppälä, MD,PhD
E
Elli Toivonen, MD,PhD
How is the study designed?
Study Type
OBSERVATIONAL
Masking
N/A
Allocation
N/A
Model
N/A
Primary Purpose
N/A
Number of Arms
4
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