None listed
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: 1.20-49 years 2. Not consuming weight reducing medicine and any nutritional supplements like multivitamins and multi-minerals. 3. Not suffering from chronic disease, capable of active communication will be selected for the study.
Exclusion criteria
Exclusion criteria: •The respondents will be having an infectious disease, functional abnormalities of the kidney and liver. •Any chronic illness, hormonal abnormalities will be excluded from the study. •Pregnant women
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Primary outcome measures the prevalence of obesity by measuring anthropometric indices and also measures prevalence of anemia by haemoglobin levelsTimepoint: 6 months | — |
Secondary
| Measure | Time frame |
|---|---|
| Secondary outcome measures include blood levels of iron status parameters will be compared between the two groups of obese and normal matching control women after screening for obesity supplementation.Timepoint: 6-8 months | — |
Countries
India
Contacts
Centre of Food Technology, University of Allahabad