Clinical Trial

Nutritional Educational Program On Therapy in Iron Deficiency Anemia

Study acronym: NEPOT-IDA
Active, Not Recruiting
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Summary
The goal of this clinical trial is to evaluate whether a Nutritional Educational Program for caregivers can improve their knowledge and performance in managing iron deficiency anemia (IDA) in children, compared to oral iron therapy alone. The study focuses on children with IDA, particularly in \[age range 1-5 years\], and aims to determine if combining nutritional education with oral iron therapy has a greater impact on improving hemoglobin levels than iron therapy alone. The main questions it aims to answer are: 1. Does caregiver education improve children's hemoglobin levels more effectively than oral iron therapy alone? 2. Does nutritional education improve caregiver knowledge and practices regarding iron-rich diets? Researchers will compare children who receive both caregiver education and oral iron therapy to those receiving only oral iron therapy to assess differences in hemoglobin levels. Participants will: Receive oral iron supplements. Caregivers will participate in educational sessions on dietary strategies to manage IDA.
Protocol Amendment History 2 changes
notable Enrollment increased: 150 -> 180 participants 2026-07-24
minor Trial arms changed: 2 -> 3 2026-07-24
Trial Details
NCT Number NCT06642337
Lead Sponsor Hawler Medical University
Conditions Iron Deficiency Anemia (IDA), Nutrition Disorders, Growth Retardation
Enrollment 180 participants
Start Date 2025-02-01
Primary Completion 2026-09-01 (estimated)
Study Completion 2026-11-01 (estimated)
Updated on ClinicalTrials.gov 2026-07-23