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Impact Assessment of Iron and Folic Acid Supplementation With and Without Intensive Health Education in Pregnant Women

Impact Assessment of Iron and Folic Acid Supplementation With and Without Intensive Health Education in Pregnant Women of Selected Villages in District Etawah: An Interventional Study

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2023/01/048956
Enrollment
100
Registered
2023-01-12
Start date
Unknown
Completion date
Unknown
Last updated
2023-09-18

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Health Condition 1: O990- Anemia complicating pregnancy, childbirth and the puerperium

Interventions

Intervention1: health education: every month there will be educational session, this will continue for 6 months Control Intervention1: nothing it will be act as control group: this group will be compa

Sponsors

none
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: pregnant women

Exclusion criteria

Exclusion criteria: 1. Women who are severely anaemic (Blood Hb level 2. Women with any known haematological disorder 3. Women who were unwilling to participate in the study

Design outcomes

Primary

MeasureTime frame
To assess the effect of iron folic acid supplementation in pregnant women, with and without intensive health educationTimepoint: 6 months—

Secondary

MeasureTime frame
To evaluate the changes in the hematological profile of the study subjects.Timepoint: 6 months—

Countries

India

Contacts

Public ContactDr Gaurav Kumar

Uttar Pradesh University of Medical Sciences

vidyarims@gmail.com9720550369

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Feb 4, 2026