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Oral nutritional supplement to support weight and length gain in stunted children aged 12 to 18 months in Palembang, Indonesia

Impact of an oral nutritional supplement on linear growth velocity in stunted children aged 12 to 18 months in Palembang City: a quasi-experimental single-arm study

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ISRCTN
Registry ID
ISRCTN18275142
Enrollment
72
Registered
2026-05-20
Start date
2025-01-02
Completion date
Unknown
Last updated
2026-06-01

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

Conditions

Stunting in children aged 12 to 18 months Nutritional, Metabolic, Endocrine

Interventions

Participants receive a milk-based oral nutritional supplement (ONS) with an energy density of 1 kcal/ml, a protein-energy ratio (PER) of 13% and 0% sucrose. The product is administered as two servings
a dietary assessment is performed at baseline and Month 5, and growth biomarkers are measured in a sub-sample of participants.

Sponsors

Nestlé (Indonesia)
Lead Sponsor

Eligibility

Sex/Gender
All
Age
12 Months to 18 Months

Inclusion criteria

Inclusion criteria: 1. Children aged 12 to 18 months at the time of enrollment 2. Stunted children, defined as height-for-age Z-score (HAZ) between <2 and =-3 SD according to WHO growth standards 3. Parent(s)/legal guardian(s) willing to provide written informed consent and to allow participation for up to 6 months 4. Willingness to comply with study product administration as prescribed by a pediatrician 5. Ability and willingness to comply with all study procedures and protocol requirements 6. Managed as outpatients and under regular monitoring by pediatrician

Exclusion criteria

Exclusion criteria: 1. Children with short stature not classified as stunting (=-2 SD) 2. Presence of chronic or major medical conditions that may affect growth or feeding, including but not limited to: tuberculosis, prematurity, small for gestational age (SGA), congenital heart disease, or other significant acute/chronic illnesses 3. Requirement for hospitalisation at the time of screening or during enrolment 4. History of cow’s milk protein allergy (CMPA) or lactose intolerance

Countries

Indonesia

Contacts

Public ContactRheinhard Rheinhard
rheinhard@equilab-int.com+62 (0)89694315561

Outcome results

None listed

Source: ISRCTN (via WHO ICTRP) · Data processed: Jun 11, 2026