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Adherence to Oral Iron and Folic Acid Supplementation Amongst Pregnant women

A Mixed Method Interventional Study to Assess the Adherence to Oral Iron and Folic Acid Supplementation Amongst Pregnant women in Rural Area of Central India - NIL

Status
Active, not recruiting
Phases
Phase 3Phase 4
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2024/10/075421
Enrollment
456
Registered
2024-10-17
Start date
Unknown
Completion date
Unknown
Last updated
2024-11-11

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

Conditions

Health Condition 1: O093- Supervision of pregnancy with insufficient antenatal care

Interventions

Intervention1: Behavioural change model: The study aims to provide health education and counseling to pregnant women in PHCs and Anganwadi Centres (AWCs) on iron deficiency anemia, oral iron-rich food

Sponsors

Dr Abhishek Joshi
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1 Pregnant women with HB greater than 10 registered with Primary Health centers 2 Those participants who have no plan to shift for the next 1 year 3 Those who give written informed consent

Exclusion criteria

Exclusion criteria: 1 Those Pregnant women who are diagnosed with moderate or severe anemia 2 Those Pregnant women who are diagnosed with Sickle cell anemia and Thalassemia shall be referred for appropriate treatment and will be excluded from the study

Design outcomes

Primary

MeasureTime frame
1 Consumption and compliance to IFA and Iron rich foods 2 Improvement in Knowledge and Awareness Attitude Behavior regarding Anemia and Compliance to ANC clinic visits 3 Determinants influencing compliance and non compliance in regards to IFA consumption Timepoint: Data will be verified once in 12 months

Secondary

MeasureTime frame
The study could investigate a number of factors that influence compliance including sociodemographic characteristics age education and socioeconomic level awareness of the value of supplements access to healthcare experiences with side effects and perceptions of the advantagesTimepoint: Data will be verified once in 12 months

Countries

India

Contacts

Public ContactDr Ragini Kulkarni

ICMR National Institute for Research in Reproductive and Child Health

kulkarnir120@gmail.com9820966112

Outcome results

None listed

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