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Standardized Corn-Soy Blend with Nutrition Education versus Nutrition Education Alone in Community-based Management of Children Under Five Years of Age with Moderate Acute Malnutrition

Standardized Corn-Soy Blend with Nutrition Education versus Nutrition Education Alone in Community-based Management of Children Under Five Years of Age with Moderate Acute Malnutrition: A Randomized Controlled Clinical Trial

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
PACTR
Registry ID
PACTR202002462358066
Enrollment
160
Registered
2020-02-18
Start date
2020-03-02
Completion date
Unknown
Last updated
2026-09-14

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

Conditions

Nutritional, Metabolic, Endocrine

Interventions

Nutrition education alone
Standardized corn soy blend with nutrition education

Sponsors

University of Uyo
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1. Children aged 6 – 59 months with MAM (weight-for-height/age between -2 and -3 Z scores or MUAC 11.5 cm – 12.5 cm). 2. Children whose parents/guardian consent to their participation and agree to bring the children/wards to the health facility throughout the period of the study.

Exclusion criteria

Exclusion criteria: 1. Children with chronic illnesses that may affect growth {(cardiac disease, renal disease, tuberculosis (chronic cough, history of contact with an adult with chronic cough, poor growth, chest infection not responding to antibiotics) liver disease, HIV/AIDS} 2. Children with feeding difficulties eg. gastroesophageal reflux diseases, cleft palate 3. Children with diarrhea (history of passage of = 3 loose stools/day), signs of dehydration or loss of appetite will be considered as complication of malnutrition. 4. Children with neurological diseases eg. Cerebral palsy 5. Children less than 6 months or more 59 months of age

Design outcomes

Primary

MeasureTime frame
To determine the; •Improvement from baseline of weight-for-height at two weekly intervals for six months follow-up duration. •The compare the proportion of recovery from MAM in the intervention arm versus the control arm.

Secondary

MeasureTime frame
To determine the; • Change in mid upper arm circumference from baseline • The proportion of non-recovery from MAM • Time-to-recovery from MAM • Time-to-progression from MAM to SAM • Change in serum protein from baseline • Change in haematocrit value from baseline • Change in serum electrolyte, urea and creatinine values from baseline • All-cause- mortality Adverse events

Countries

Nigeria

Contacts

Public ContactFrances Okpokoworuk

Consultant Cardiologist University of Uyo Teaching Hospital

zipsadoo@yahoo.com+2348037270377

Outcome results

None listed

Source: PACTR (via WHO ICTRP) · Data processed: Sep 19, 2026