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Public Health Initiative to study the role of Ayurveda in improving Hemoglobin level in women of reproductive age in Chengalpattu district of Tamilnadu

A community based study to assess the role of Ayurvedic interventions and lifestyle advocacy on Iron Deficiency Anemia in women of reproductive age in Chengalpattu district of Tamilnadu - NIL

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2025/06/088988
Enrollment
1120
Registered
2025-06-17
Start date
Unknown
Completion date
Unknown
Last updated
2025-06-24

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

Conditions

Health Condition 1: D509- Iron deficiency anemia, unspecified

Interventions

None listed

Sponsors

Ministry of Ayush
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Non-pregnant non-lactating women of reproductive age(15 to 49years),Hb greater than or equal to 8 gm percentage and less than 12 gm percentage,intend to remain in the study site for the next 6 months atleast, willingness to sign the informed consent form(Written assent in participants below 18 years of age) and to participate in the study related activities such as adherence to lifestyle advocacy,study intervention, logging in compliance log, etc.

Exclusion criteria

Exclusion criteria: Severe anemia(less than 8gm percentage) warranting immediate referral and care, history of diagnosis of other types of anemia, Women with menstrual irregularities such as menorrhagia, irregular menstrual cycles, cycle duration less than 24 days, History of any chronic or other medical condition (e.g. IBS, IBD, malignancy) requiring frequent medical attention or potentially interfering with nutritional status, malnutrition warranting medical attention, Obesity (BMI greater than or equal to 29.9),any chronic or acute illness that require intake of any other medications other than oral hypoglycemic agents or anti-hypertensive, any other condition that, as per the PI would adversely affect participation in the study or the outcome of the study.

Design outcomes

Primary

MeasureTime frame
Change in Hemoglobin levelTimepoint: To be assessed during baseline,90thday and 180th Day

Secondary

MeasureTime frame
1.Change in the other blood indices such as RBC Count, MCV, MCHC, and PCV 2.Change in Serum Ferritin level 3.Medication adherence and compliance to lifestyle advocacy 4.Documentation of demographic characteristics and severity of anemia through pre-designed questionnaire to assess the association between both Timepoint: 1. To be assessed during baseline,90thday and 180th Day 2. To be assessed during baseline,90thday and 180th Day 3. To be assessed during 30th, 60th and 90th day 4.To be assessed during Baseline

Countries

India

Contacts

Public ContactDr S Asha

CCRAS-Dr. Achanta Lakshmipathi Regional Ayurveda Research Institute

dr.ashas2324@gmail.com9895192067

Outcome results

None listed

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