Description Module
The Description Module contains narrative descriptions of the clinical trial, including a brief summary and detailed description. These descriptions provide important information about the study's purpose, methodology, and key details in language accessible to both researchers and the general public.
Description Module path is as follows:
Study -> Protocol Section -> Description Module
Description Module
Ignite Creation Date:
2025-12-24 @ 5:48 PM
Ignite Modification Date:
2025-12-24 @ 5:48 PM
NCT ID:
NCT04810468
Brief Summary:
Study of malnutrition in primary school age children aim to asses the prevelance of malnutrition amoung the children in this age group and also ldintified the factors that affect in malnutrition between the children and the study will done in two primary school one present in rural area and another in urban area to compare the factor and the result that affect in both two different area
Detailed Description:
Study of malnutrition in primary school age children aim to asses the prevelance of malnutrition amoung the children in this age group and also ldintified the factors that affect in malnutrition between the children and the study will done in two primary school one present in rural area and another in urban area to compare the factor and the result that affect in both two different area investigators in this study will use anthropometric measurment to asses wheight and height and BMI and also collect sociodemographic data from participant for Ex father and mother education and age ,sex,place of residence,father and mother jop, mean income.
and also collect data about hygine lnformation for Ex safe and cleen drink water , presence of toilet ,wash hand before and after eating and cooking ,clean nail .
Other data will be collected from participant about dietary habits for Ex how many times eating meat, paultary ,fish in week and how many times eating vegetable,fruits ege milk in day .
This all data will be analysed by use the proper statical analysis system and finally the results will obtained
Study:
NCT04810468
Study Brief:
Protocol Section:
NCT04810468