Maternal Education on Complementary Feeding and Infant Outcome

• Nutritional status [ Time Frame: 7.5 month ] [ Designated as safety issue: No ]
  Height, Weight and Mid Upper Arm circumference
  
  

• Diarrhea episodes [ Time Frame: 7.5 months ] [ Designated as safety issue: No ]
  Diarrhea episodes during the study period.
  
  
• Z score (HAZ, WAZ and WHZ scores) [ Time Frame: 7.5 months ] [ Designated as safety issue: No ]
  Z scores (wasting, stunting will be measured and compared in between interventional and control group.
  
  
• ARI [ Time Frame: 7.5 months ] [ Designated as safety issue: No ]
  ARI will be asses by using standard IMCI guidelines, and/or physician prescription and medications prescribed to the infant.
  
  

Study population The study will be conducting in Bhainse colony (BC), Karachi. This is a periurban community area, and catering population mainly belonging to low - middle income households. The study population would be the mothers (having infant of 2.5 - 5 months of age) and their infants in these two study areas.

Inclusion Criteria;

• Infants aged 2.5 - 5 months; who are either exclusively breast feed or partially breast feed but have not started complementary feeding or have recently started complementary food (less than 1 week)
• Informed consent Exclusion Criteria;
• Infants found below 5th percentile on weight for age CDC growth charts 23 at baseline will be excluded.
• History of two or more hospital admissions for more than 7 days each
• Presence of serious congenital anomalies (cleft palate, congenital heart disease, neural tube defect) or other chronic conditions impairing feeding (e.g. cerebral palsy)
• Presence of acute illness requiring urgent hospitalization
• Infants from families of very low socioeconomic status where adequate calorie-provision is constrained (assessed by a questionnaire on household possessions of items such as mobile phone, bicycle or other vehicle, TV, cemented construction, fuel used for cooking - wood or gas/LPG)
• Infant already enrolled in any trial with a nutritional intervention will be excluded.
• Infants who at initial clinical examination are found to be severely anemic.

Data outcome measures Measuring Weight, height and Mid-upper arm circumference The investigators measure serial height, weight and mid-upper arm circumference (MUAC) for each subject at enrollment and subsequently in each visit. Each infant will be measured four times during the study enrollment.

• Height will be measured twice and the results averaged. Duplicate measures that exceed predefined allowable variation will be resolved by the field supervisor, e.g., by returning to the site with the interviewer to repeat the measurements. The height of infants will be measured (to the nearest 0.1 cm) in the recumbent position using a board with a fixed head and sliding foot piece.
• Weight will be measured to the nearest 0.1 kg using a scale that is calibrated daily.

• MUAC will be measure twice each time by using measuring tape. All anthropometric measurements will be taken three times (in each visit) and the mean of the measurements will counted as valid value. Each of the anthropometric indices will be expressed in standard deviation units (SD) from the median of the NCHS/CDC/WHO International Reference Population. Methods are adapted from How to Weigh and Measure Children: Assessing the Nutritional Status of Young Children in Household Surveys, United Nations Department of Technical Cooperation for Development and Statistical Office, 1986. The height and weight measurements will later converted into WAZ, WHZ and HAZ score and the difference in both groups will be analyzed.

  • ARI will be measured through standard IMCI guidelines. ARI could be assess by the physician's visit and treatment prescribed.