Evaluation of an Intervention Program for the Prevention of Anemia
Primary Purpose
Anemia
Status
Unknown status
Phase
Not Applicable
Locations
Israel
Study Type
Interventional
Intervention
Iron supplement
Sponsored by
About this trial
This is an interventional prevention trial for Anemia focused on measuring Anemia, Iron, Supplement
Eligibility Criteria
Inclusion Criteria:
- Infant who visit Family Health Centers
Sites / Locations
- Tel Aviv District of the Health Office
Outcomes
Primary Outcome Measures
Secondary Outcome Measures
Full Information
NCT ID
NCT00436202
First Posted
February 15, 2007
Last Updated
September 12, 2010
Sponsor
Wolfson Medical Center
Collaborators
Tel Aviv District of the Health Office
1. Study Identification
Unique Protocol Identification Number
NCT00436202
Brief Title
Evaluation of an Intervention Program for the Prevention of Anemia
Study Type
Interventional
2. Study Status
Record Verification Date
September 2010
Overall Recruitment Status
Unknown status
Study Start Date
undefined (undefined)
Primary Completion Date
undefined (undefined)
Study Completion Date
undefined (undefined)
3. Sponsor/Collaborators
Name of the Sponsor
Wolfson Medical Center
Collaborators
Tel Aviv District of the Health Office
4. Oversight
5. Study Description
Brief Summary
The purpose of the study is to determine whether improvement in the accessibility to iron supplement will decrease anemia rates in infants.
Detailed Description
Iron deficiency anemia is the most common type of anemia in infants, children and women of reproductive age. The most frequent cause of iron deficiency in infants at 6 months of life is poor nutrition during a period of rapid growth and a diet lacking in iron rich foods. Children who suffered from anemia in infancy demonstrated slower cognitive development, were low achievers in school and had a high rate of behavioral disturbances.
The Ministry of Health implements a primary prevention program for anemia. If by making iron supplements more accessible would increase parental compliance in acquisition of the iron supplement and subsequently reduce the rate of iron deficiency anemia, the result would be the immediate application of the finding. It is possible to implement a program whereby the supplement will be directly available at the family health centers for purchase by the parent.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Anemia
Keywords
Anemia, Iron, Supplement
7. Study Design
Primary Purpose
Prevention
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Non-Randomized
8. Arms, Groups, and Interventions
Intervention Type
Behavioral
Intervention Name(s)
Iron supplement
10. Eligibility
Sex
All
Minimum Age & Unit of Time
4 Months
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria:
Infant who visit Family Health Centers
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Tamar Shohat, M.D., MPH
Organizational Affiliation
Tel Aviv District of the Health Office
Official's Role
Principal Investigator
Facility Information:
Facility Name
Tel Aviv District of the Health Office
City
Tel Aviv
Country
Israel
12. IPD Sharing Statement
Learn more about this trial
Evaluation of an Intervention Program for the Prevention of Anemia
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