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Stunting and Targeting Reduction of Impaired Growth in Kids Effectively

Stunting and Targeting Reduction of Impaired Growth in Kids Effectively

Recruiting
1-5 years
All
Phase N/A

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Overview

The objective of this prospective, real-world evidence/pragmatic study with a quality improvement program approach is to evaluate the feasibility and effectiveness of a community-engaged nutrition-focused program utilizing nutrition screening, education, supplementation and continuous follow up for children and their families.

Eligibility

Household Component

Inclusion

  • Children aged 1-5 years experiencing stunting or its risk (defined as HAZ ≤ -1 SD at baseline)
  • Children's legal guardian agrees to participate in the study
  • Full term pregnancy (defined as ≥ 37 weeks gestation and ≥ 2500g birth weight)
  • Residence in study area attending Children International (NGO) centers

Exclusion

• Children who have current medical conditions requiring hospitalization: gastrointestinal tract infections or inflammatory bowel disease; active tuberculosis; acute hepatitis B or C; human immunodeficiency virus OR malignancy; cystic fibrosis; immunodeficiency syndromes, congenital abnormalities of the respiratory tract, such as lung and respiratory cilia; an unsuspected foreign body in the respiratory tract; asthma; heart abnormalities; abdominal hernias; and known metabolic disorders, renal impairment, or rheumatic diseases and diabetes

  • Congenital condition
  • Children with disabilities such as cerebral palsy, autism spectrum disorder, neurodegenerative disorders
  • Children with chronic or acute infections e.g. HIV, malaria
  • Children who are taking medications or other agents that could potentially affect body weight, including diuretics, appetite stimulants, steroids, and growth hormones
  • Children who have genetic conditions impacting weight status such as but not limited to: Bardet-Biedl Syndrome, Prader-Willi Syndrome
  • Children already enrolled in a nutrition program that includes a supplement
  • Participant has an allergy or intolerance to any ingredient in the study supplement, as reported by the parent.
  • Children with sleep disorders such as but not limited to: obstructive sleep apnea, insomnia, parasomnias (sleepwalking, night terrors, bedwetting), delayed sleep phase syndrome, behavioral sleep disorders, circadian rhythm disorders
  • Mental health disorders such as but not limited to: anxiety, depression

Organization Component

Inclusion

  • NGO staff taking part in nutrition screenings
  • Agrees to participate in survey

Exclusion

  • Not involved in the implementation of the study
  • Not involved in working with pediatric stunting or its risk
  • Declines participation in survey

Study details
    Malnutrition (Calorie)

NCT07524907

Abbott Nutrition

25 July 2026

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FAQs

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