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Folic Acid and Vitamin B12 in Young Indian Children

Primary Purpose

Diarrhea, Pneumonia

Status
Completed
Phase
Phase 2
Locations
India
Study Type
Interventional
Intervention
Folic Acid
Vitamin B12
Placebo
Folic acid and vitamin B12
Sponsored by
Tor A. Strand
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional prevention trial for Diarrhea focused on measuring Nutrition, Children, Folate, Vitamin B12, India, Homocysteine, Methyl Malonic Acid

Eligibility Criteria

6 Months - 30 Months (Child)All SexesAccepts Healthy Volunteers

Inclusion Criteria:

  • Age: 6 to 30 months
  • Either sex
  • Likely to reside in area for next 6 months

Exclusion Criteria:

  • Severe systemic illness requiring hospitalization
  • Severe malnutrition, i.e. weight for height < -3 z of the WHO standard for this age group. For ethical reasons these children require micronutrient supplementation and adequate medical care.
  • Non consent
  • Consuming vitamin supplements that include folic acid and vitamin B12.
  • Severe anemia (Hb < 7 g/dL).

Sites / Locations

  • Society for Essential Health Action and Training

Arms of the Study

Arm 1

Arm 2

Arm 3

Arm 4

Arm Type

Placebo Comparator

Experimental

Experimental

Experimental

Arm Label

A

B

C

D

Arm Description

Placebo dietary supplement

Folic acid

Vitamin B12

Folic acid and Vitamin B12

Outcomes

Primary Outcome Measures

Number of episodes diarrhea (all, severe, prolonged) and pneumonia (ALRI, Clinical pneumonia)
Prevalence of diarrhea

Secondary Outcome Measures

Growth (length for age, weight for age, and length for weight)
Adverse events (vomiting and gastric discomfort)
Changes in folate, vitamin B12, methyl malonic acid, and homocysteine concentration
Developmental Milestones
Developmental milestones. The developmental milestones will be measured using the ASQ-3. ASQ-3 is an easily administered and comprehensive checklist consisting of 30 items measuring skills in 5 different domains; Communication, Gross Motor, Fine Motor, Personal-Social and Problem-Solving. The questionnaires are divided into two-month intervals for use with children 4-60 months of age, and scores are normed to indicate whether children are developing age-appropriately.
Measure the association between pneumonia incidence and the plasma mannose binding lectin (MBL) concentration
Measure the exposure to Cryptosporidium spp
We will measure the exposure to Cryptosporidium spp. in Indian children aged 6-30 months by measurement of antibodies to recombinant gp15, a conserved surface protein in plasma samples taken at baseline.
Measure the association between the antibody response to Cryptosporidium and plasma MBL
Compare the change in plasma MBL between the intervention groups
We will compare the change in plasma MBL between those who have been given 2 RDA of vitamin B12 and/or folic acid with those who were given placebo in a subsample of 256 children.
Vitamin D status
We will measure vitamin D (25-hydroxy vitamin D) in all children at baseline to describe the vitamin D status and the proportion with vitamin D deficiency.
Vitamin D status and the risk for respiratory infections
We will measure the vitamin D status at baseline and assess to what extent it predicts the risk of subsequent respiratory tract infections over the next 6 months.

Full Information

First Posted
July 16, 2008
Last Updated
July 27, 2015
Sponsor
Tor A. Strand
Collaborators
Society for Essential Health Action and Training, New Delhi, India, Thrasher Research Fund
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1. Study Identification

Unique Protocol Identification Number
NCT00717730
Brief Title
Folic Acid and Vitamin B12 in Young Indian Children
Official Title
Routine Administration of Folic Acid and Vitamin B12 to Prevent Childhood Infections in Young Indian Children
Study Type
Interventional

2. Study Status

Record Verification Date
July 2015
Overall Recruitment Status
Completed
Study Start Date
January 2010 (undefined)
Primary Completion Date
September 2011 (Actual)
Study Completion Date
September 2011 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor-Investigator
Name of the Sponsor
Tor A. Strand
Collaborators
Society for Essential Health Action and Training, New Delhi, India, Thrasher Research Fund

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
Hypothesis: Supplementation of two recommended daily allowances (RDA) of folic acid with or without simultaneous administration of vitamin B12 reduces the rates of acute lower respiratory tract infections (ALRI), clinical pneumonia and diarrhea. Design/Methods We will conduct a preventive randomized placebo controlled clinical trial of folic acid and vitamin B12 supplementation in 1000 children aged 6 to 30 months living in a low to middle-income socioeconomic setting in New Delhi, India. Children aged 6-30 months will be identified through a survey. Eligible and willing Children aged 6-30 months will be randomized to 4 treatment groups. Trial to enrollment informed consent will be obtained by the Study Physician/Supervisor. At enrollment a baseline form will be filled and the child weight and length taken. The baseline blood samples will be collected. The supplements will be given daily for 6 months. Morbidity will be ascertained through biweekly home visits by field workers.
Detailed Description
Pneumonia and diarrhea are among the leading causes of poor health and death in young children of developing countries. Many of these children have inadequate intakes of several vitamins and minerals. Folate and vitamin B12 are important for normal function of the immune system. Deficiencies of these vitamins are often part of general malnutrition and might be responsible for the excess morbidity and mortality seen in malnourished children. In a recent cohort study in almost 2,500 Indian children we demonstrated that those with poor folate status had higher rates of diarrhea and pneumonia. This study also showed that children that were not breastfed had poor folate status and our analyses suggested that the effect of breastfeeding in preventing respiratory and gastrointestinal infections could be explained by the folate content of breast milk. The finding that poor folate status is related to increased susceptibility to childhood infections needs to be confirmed in well conducted clinical trials in populations where folate deficiency is prevalent. This trial aims to examine whether daily supplementation of 2 recommended doses of folate or vitamin B12 or both will lessen the incidence of acute lower respiratory tract infections and diarrhea. We will also measure if the supplementation improves the weight and length of supplemented children.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Diarrhea, Pneumonia
Keywords
Nutrition, Children, Folate, Vitamin B12, India, Homocysteine, Methyl Malonic Acid

7. Study Design

Primary Purpose
Prevention
Study Phase
Phase 2
Interventional Study Model
Factorial Assignment
Masking
ParticipantCare ProviderInvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
1000 (Actual)

8. Arms, Groups, and Interventions

Arm Title
A
Arm Type
Placebo Comparator
Arm Description
Placebo dietary supplement
Arm Title
B
Arm Type
Experimental
Arm Description
Folic acid
Arm Title
C
Arm Type
Experimental
Arm Description
Vitamin B12
Arm Title
D
Arm Type
Experimental
Arm Description
Folic acid and Vitamin B12
Intervention Type
Dietary Supplement
Intervention Name(s)
Folic Acid
Other Intervention Name(s)
Folate
Intervention Description
150µgm/day for 6 months in children older than 11 months and 80µgm in 6 to 11 months.
Intervention Type
Dietary Supplement
Intervention Name(s)
Vitamin B12
Other Intervention Name(s)
Cobalamin
Intervention Description
1.8µgm/day for 6 months in children older than 11 months and 0.5µgm in 6 to 11 months.
Intervention Type
Dietary Supplement
Intervention Name(s)
Placebo
Intervention Description
Placebo with no active ingredients
Intervention Type
Dietary Supplement
Intervention Name(s)
Folic acid and vitamin B12
Intervention Description
Folic acid 150µgm/day for 6 months in children older than 11 months and 80µgm in 6 to 11 months vitamin B12 1.8µgm/day for 6 months in children older than 11 months and 0.5µgm in 6 to 11 months.
Primary Outcome Measure Information:
Title
Number of episodes diarrhea (all, severe, prolonged) and pneumonia (ALRI, Clinical pneumonia)
Time Frame
6 months
Title
Prevalence of diarrhea
Time Frame
6 months
Secondary Outcome Measure Information:
Title
Growth (length for age, weight for age, and length for weight)
Time Frame
6 month
Title
Adverse events (vomiting and gastric discomfort)
Time Frame
6 months
Title
Changes in folate, vitamin B12, methyl malonic acid, and homocysteine concentration
Time Frame
6 months
Title
Developmental Milestones
Description
Developmental milestones. The developmental milestones will be measured using the ASQ-3. ASQ-3 is an easily administered and comprehensive checklist consisting of 30 items measuring skills in 5 different domains; Communication, Gross Motor, Fine Motor, Personal-Social and Problem-Solving. The questionnaires are divided into two-month intervals for use with children 4-60 months of age, and scores are normed to indicate whether children are developing age-appropriately.
Time Frame
End study, i.e. after 6 months of vitamin B12 and/or folic acid administration
Title
Measure the association between pneumonia incidence and the plasma mannose binding lectin (MBL) concentration
Time Frame
Baseline blood samples
Title
Measure the exposure to Cryptosporidium spp
Description
We will measure the exposure to Cryptosporidium spp. in Indian children aged 6-30 months by measurement of antibodies to recombinant gp15, a conserved surface protein in plasma samples taken at baseline.
Time Frame
Baseline blood samples
Title
Measure the association between the antibody response to Cryptosporidium and plasma MBL
Time Frame
Baseline blood samples
Title
Compare the change in plasma MBL between the intervention groups
Description
We will compare the change in plasma MBL between those who have been given 2 RDA of vitamin B12 and/or folic acid with those who were given placebo in a subsample of 256 children.
Time Frame
6 months
Title
Vitamin D status
Description
We will measure vitamin D (25-hydroxy vitamin D) in all children at baseline to describe the vitamin D status and the proportion with vitamin D deficiency.
Time Frame
Baseline blood samples
Title
Vitamin D status and the risk for respiratory infections
Description
We will measure the vitamin D status at baseline and assess to what extent it predicts the risk of subsequent respiratory tract infections over the next 6 months.
Time Frame
Baseline samples and 6 months follow up

10. Eligibility

Sex
All
Minimum Age & Unit of Time
6 Months
Maximum Age & Unit of Time
30 Months
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria: Age: 6 to 30 months Either sex Likely to reside in area for next 6 months Exclusion Criteria: Severe systemic illness requiring hospitalization Severe malnutrition, i.e. weight for height < -3 z of the WHO standard for this age group. For ethical reasons these children require micronutrient supplementation and adequate medical care. Non consent Consuming vitamin supplements that include folic acid and vitamin B12. Severe anemia (Hb < 7 g/dL).
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Tor A Strand, MD, PhD
Organizational Affiliation
University of Bergen
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Sunita Taneja, MBBS, PhD
Organizational Affiliation
Society for Essential Health Action and Training
Official's Role
Principal Investigator
Facility Information:
Facility Name
Society for Essential Health Action and Training
City
New Delhi
State/Province
Delhi
Country
India

12. IPD Sharing Statement

Citations:
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Citation
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Folic Acid and Vitamin B12 in Young Indian Children

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