Stunting and Targeting Reduction of Impaired Growth in Kids Effectively
ConditionMalnutrition (Calorie)
Trial statusNot yet recruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age1-5
SponsorAbbott Nutrition
About this trial
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 criteria
Qualifiers
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
Disqualifiers
None
Trial design
Treatments tested in this trial
- Not listed
Trial groups
150 Participants
are grouped into 2 trial groupsSponsors and collaborators
Abbott Nutrition
Lead sponsor
Children International
Collaborator
Source ClinicalTrials.gov