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Stunting and Targeting Reduction of Impaired Growth in Kids Effectively

RecruitingObservational study

STRIKE: Stunting and Targeting Reduction of Impaired Growth in Kids Effectively: A Community Engaged Comprehensive, Multi-Faceted Nutrition Quality Improvement Program

Who can join

Ages 1 to 5 · All sexes

Full eligibility criteria
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

About the study

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.

Sponsor: Abbott Nutrition · Participants: 158 · Started: May 11, 2026

Contact the study team

Official record on ClinicalTrials.gov — NCT07524907

Locations in the U.S.

MissouriChildren International, Kansas City

Conditions

From ClinicalTrials.gov, data retrieved Sep 30, 2026. Each study sets its own eligibility; the study team decides who can join.