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Malnutrition At Risk intervention for Visible and Effective Long-term growth

Malnutrition At Risk intervention for Visible and Effective Long-term growth

Status
Active, not recruiting
Phases
Phase 2Phase 3
Study type
Interventional
Source
TCTR
Registry ID
TCTR20220908004
Enrollment
160
Registered
2022-09-08
Start date
2022-09-20
Completion date
Unknown
Last updated
2026-08-03

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

Conditions

Malnutrition-at-risk children aged 1-6 years malnutrition-at-risk children undernutrition wasting

Interventions

Giving 2 portions per day of oral nutritional supplement formula together with dietary advice. Each portion of the oral nutritional supplement provides 210 kcal per portion with protein 5.5 g, iron, z
Experimental Dietary Supplement,Sham Comparator Other
Oral nutritional supplements ,Dietary counselling alone

Sponsors

Pediatric Nutrition Research Unit, Pediatric Department, Faculty of Medicine, Chulalongkorn University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
1 Years to 6 Years

Inclusion criteria

Inclusion criteria: 1. children aged 1-6 years old 2. weight-for-height between -1SD to -2SD 3. born full-term with birth weight 2.5 kg to 4.5 kg 4. parent(s) has sufficient Thai language skills to understand the study information, the informed consent, and to comply with the study procedure 5. parent(s) is willing and deemed able to fulfill the requirements of the study protocol and procedures 6. at least one parent is of legal age of consent

Exclusion criteria

Exclusion criteria: 1. a child who is diagnosed with diseases that might affect growth (e.g., chronic infectious disease, neoplastic diseases, renal, hepatic, cardiovascular diseases, malabsorption syndrome, or a diagnosis of congenital disorder) 2. a child who is receiving medications that interfere with appetite, nutrient absorption, or child growth 3. participation in any other interventional trial during the same period 4. cow milk allergy or intolerance

Design outcomes

Primary

MeasureTime frame
Weight at 1, 3, 6 months after starting the intervention kg,Height at 1, 3, 6 months after starting the intervention cm

Secondary

MeasureTime frame
body composition 3,6 months after starting the intervention BIA,iron, zinc and anemic status 3,6 months after starting the intervention blood test,feeding difficulty 1, 3, 6 months after starting the intervention Montreal Children Hospital Feeding Scale,feeding behavior 1,3,6 months after starting the intervention Children Eating Behavior Questionnaire ,Appetite score 1,3, 6 months after starting the intervention visual analog scale,Other health outcomes e.g. sleep duration, defecation pattern, infection episodes, parental satisfaction 1,3,6 months after starting the intervention questionnaire

Countries

Thailand

Contacts

Public ContactSirinuch Chomtho

Faculty of Medicine, Chulalongkorn University

sirinuch.c@chula.ac.th6622564903

Outcome results

None listed

Source: TCTR (via WHO ICTRP) · Data processed: Aug 9, 2026