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Healthy Infant Development Project

Primary Purpose

Iron Deficiency Anemia, Iron Deficiency

Status
Completed
Phase
Not Applicable
Locations
China
Study Type
Interventional
Intervention
folic acid + iron prenatally, vits A & D + iron postnatally
folic acid + iron prenatally, vitamins A & D postnatally
folic acid prenatally, vitamins A & D + iron postnatally
folic acid prenatally, vitamins A & D postnatally
Sponsored by
Eunice Kennedy Shriver National Institute of Child Health and Human Development (NICHD)
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional prevention trial for Iron Deficiency Anemia focused on measuring iron deficiency anemia, iron deficiency, infant, development, behavior

Eligibility Criteria

1 Day - 5 Days (Child)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

- Full-term healthy neonates born to study mothers from CDC's Prenatal Nutrition Study with randomly selected lot numbers.

Exclusion Criteria:

  • birth weight < 2500 g
  • gestational age ≤ 37 wk
  • major perinatal complications
  • major congenital anomaly
  • multiple birth.

Sites / Locations

  • Peking University First Hospital

Arms of the Study

Arm 1

Arm 2

Arm 3

Arm 4

Arm Type

Experimental

Experimental

Experimental

Active Comparator

Arm Label

a

b

c

d

Arm Description

pre- and early postnatal iron

iron prenatal only

iron early postnatal only

no iron pre- or postnatal

Outcomes

Primary Outcome Measures

Infant behavior and development

Secondary Outcome Measures

Infant anemia

Full Information

First Posted
February 11, 2008
Last Updated
October 28, 2014
Sponsor
Eunice Kennedy Shriver National Institute of Child Health and Human Development (NICHD)
Collaborators
Centers for Disease Control and Prevention
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1. Study Identification

Unique Protocol Identification Number
NCT00613717
Brief Title
Healthy Infant Development Project
Official Title
Timing, Duration and Severity of Infant Iron Deficiency: Developmental Impacts
Study Type
Interventional

2. Study Status

Record Verification Date
March 2014
Overall Recruitment Status
Completed
Study Start Date
November 2009 (undefined)
Primary Completion Date
June 2014 (Actual)
Study Completion Date
June 2014 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Eunice Kennedy Shriver National Institute of Child Health and Human Development (NICHD)
Collaborators
Centers for Disease Control and Prevention

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
The Healthy Infant Development Project will determine if providing micronutrient supplements to mothers during pregnancy and infants in the first 9 months fosters healthy behavior and development in babies.
Detailed Description
Iron deficiency (ID) is the most common single nutrient disorder in the world, and pregnant women and infants are at highest risk. With long-lasting differences in prior studies, effects on the developing brain and infant behavior and development are among the most worrisome concerns. The proposed study will determine developmental/ behavioral effects of preventing ID depending on timing (Aim 1) and duration (Aim 2) of iron supplementation (i.e., pre- and/or early postnatally). The study will relate outcomes to severity of ID (Aim 3) and consider reversibility of effects with iron therapy, depending on timing (Aim 4). We expect different neurobehavioral effects when ID occurs or is prevented/treated during different phases of brain development (proliferation and growth phase primarily prenatally and regional diversification and interconnection largely in infancy). The project entails 2 randomized controlled trials (RCTs) to support causal inferences about preventing ID pre- and/or early postnatally. The project builds on a large US CDC-supported study (Pregnancy Nutrition Study) involving pregnant women in rural China (ClinicalTrials.gov identifier: NCT00133744). Study groups of infants in the proposed RCTs combined are a) pre- and early postnatal iron, b) prenatal iron, c) early postnatal iron, and d) neither (n = 500/group, total 2000, at study end). Iron status and sensitive sensory, motor, cognitive, language, and social-emotional outcomes will be assessed at birth, 9 and 18 mo. Results of Aims 1 & 2 will determine the best window to prevent ID effects and whether breast-fed infants benefit from iron before 6 mo. Aim 3 (severity) will determine the level of ID at which different developmental domains are adversely affected. If ill effects of ID without anemia are documented, there could be major policy implications; screening is currently only for anemia. Detecting more or less vulnerable domains may also point to other interventions in addition to iron therapy. To identify reversibile effects, depending on age of treatment (Aim 4), outcomes at 18 mo will be compared for infants 1) never iron-deficient, 2) poor iron status at birth and assigned to postnatal iron, 3) maternal IDA (anemia) treated in the 1st or 2nd trimester, 4) infant IDA treated at 9 mo, and 5) IDA treated at 18 mo. The results will be highly relevant to global practice and policy regarding ID, which differentially affects poor and/or minority women and infants everywhere. The project is expected to continue with a 5-year follow-up (Nov 2014- Oct 2019).

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Iron Deficiency Anemia, Iron Deficiency
Keywords
iron deficiency anemia, iron deficiency, infant, development, behavior

7. Study Design

Primary Purpose
Prevention
Study Phase
Not Applicable
Interventional Study Model
Factorial Assignment
Masking
ParticipantCare ProviderInvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
2371 (Actual)

8. Arms, Groups, and Interventions

Arm Title
a
Arm Type
Experimental
Arm Description
pre- and early postnatal iron
Arm Title
b
Arm Type
Experimental
Arm Description
iron prenatal only
Arm Title
c
Arm Type
Experimental
Arm Description
iron early postnatal only
Arm Title
d
Arm Type
Active Comparator
Arm Description
no iron pre- or postnatal
Intervention Type
Dietary Supplement
Intervention Name(s)
folic acid + iron prenatally, vits A & D + iron postnatally
Intervention Description
Prenatally: pills by mouth, one per day, from the first prenatal visit until delivery, 400 mcg folic acid, 30 mg Fe. Postnatally: liquid by mouth, once per day, from 6 weeks old until 9 months old, 1 mg/kg/day Fe, 1500 IU vitamin A, 500 IU vitamin D.
Intervention Type
Dietary Supplement
Intervention Name(s)
folic acid + iron prenatally, vitamins A & D postnatally
Intervention Description
Prenatally: pills by mouth, one per day, from the first prenatal visit until delivery, 400 mcg folic acid, 30 mg Fe. Postnatally: liquid by mouth, once per day, from 6 weeks old until 9 months old, 1500 IU vitamin A, 500 IU vitamin D.
Intervention Type
Dietary Supplement
Intervention Name(s)
folic acid prenatally, vitamins A & D + iron postnatally
Intervention Description
Prenatally: pills by mouth, one per day, from the first prenatal visit until delivery, 400 mcg folic acid. Postnatally: liquid by mouth, once per day, from 6 weeks old until 9 months old, 1 mg/kg/day Fe, 1500 IU vitamin A, 500 IU vitamin D.
Intervention Type
Dietary Supplement
Intervention Name(s)
folic acid prenatally, vitamins A & D postnatally
Intervention Description
Prenatally: pills by mouth, one per day, from the first prenatal visit until delivery, 400 mcg folic acid. Postnatally: liquid by mouth, once per day, from 6 weeks old until 9 months old, 1500 IU vitamin A, 500 IU vitamin D.
Primary Outcome Measure Information:
Title
Infant behavior and development
Time Frame
9 and 18 months
Secondary Outcome Measure Information:
Title
Infant anemia
Time Frame
9 and 18 months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
1 Day
Maximum Age & Unit of Time
5 Days
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: - Full-term healthy neonates born to study mothers from CDC's Prenatal Nutrition Study with randomly selected lot numbers. Exclusion Criteria: birth weight < 2500 g gestational age ≤ 37 wk major perinatal complications major congenital anomaly multiple birth.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Betsy Lozoff, MD
Organizational Affiliation
University of Michigan
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Li Ming, MD
Organizational Affiliation
Peking University First Hospital
Official's Role
Study Director
Facility Information:
Facility Name
Peking University First Hospital
City
Beijing
ZIP/Postal Code
100034
Country
China

12. IPD Sharing Statement

Citations:
PubMed Identifier
27836288
Citation
Clark KM, Li M, Zhu B, Liang F, Shao J, Zhang Y, Ji C, Zhao Z, Kaciroti N, Lozoff B. Breastfeeding, Mixed, or Formula Feeding at 9 Months of Age and the Prevalence of Iron Deficiency and Iron Deficiency Anemia in Two Cohorts of Infants in China. J Pediatr. 2017 Feb;181:56-61. doi: 10.1016/j.jpeds.2016.10.041. Epub 2016 Nov 8.
Results Reference
derived
PubMed Identifier
26791556
Citation
Lozoff B, Jiang Y, Li X, Zhou M, Richards B, Xu G, Clark KM, Liang F, Kaciroti N, Zhao G, Santos DC, Zhang Z, Tardif T, Li M. Low-Dose Iron Supplementation in Infancy Modestly Increases Infant Iron Status at 9 Mo without Decreasing Growth or Increasing Illness in a Randomized Clinical Trial in Rural China. J Nutr. 2016 Mar;146(3):612-21. doi: 10.3945/jn.115.223917. Epub 2016 Jan 20.
Results Reference
derived

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Healthy Infant Development Project

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