Oral Nutritional Supplementation in Children at Risk of Undernutrition

Completed · Not applicable

Conditions studied: Undernutrition

In brief

The objective of this randomized, controlled trial is to evaluate the effects of consuming a pediatric oral nutritional supplement (ONS) plus dietary counseling for 120 days on anthropometric growth, strength, and nutritional status, compared with dietary counseling alone in undernourished children in the United States.

Key facts

Study ID

NCT05161000

Run by

Abbott Nutrition

People needed

279

Starts

2022-04-18

Expected to finish

2024-06-11

Last updated by the study team

2024-07-16

Who can join

Age: 3 and older, up to 9. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• Child is 36 months - 107 months of age.
• Child is undernourished as determined by BMI for age z-score or Mid-upper-arm circumference z-score
• Child's caregiver has voluntarily signed and dated an informed consent form (ICF), approved by an IRB, and provided Health Insurance Portability and Accountability Act (HIPAA) or other applicable privacy regulation authorization prior to any participation in the study.
• Child's caregiver is willing to abstain from providing non-study oral nutrition supplements during the study period duration.
• Child's caregiver is able and willing to follow study procedures and record data in parent diaries and complete any forms or assessments needed during the study.
• Child is willing to consume the study product for the duration of the study, if randomized to intervention group

You may not qualify if…

• Child has a height-for-age z-score ≥ 0.
• Child is currently drinking an oral nutritional supplement (ONS) on a regular basis (≥ 15 days in the past month)
• Child is participating in another study that has not been approved as a concomitant study by AN.
• Child has been diagnosed with the following:
• Galactosemia, or an allergy or intolerance to any ingredient found in the study product
• Acute or chronic infections including but not restricted to respiratory infections, diarrhea, Hepatitis B or C, HIV infection or tuberculosis
• Severe gastrointestinal disorders such as celiac disease, short bowel syndrome, pancreatic insufficiency, or cystic fibrosis
• Neoplastic, renal, hepatic or cardiovascular, hormonal or metabolic disorders, Down's syndrome or significant, uncorrected cardiac anomalies that may impact growth
• Infantile anorexia nervosa, developmental disability, including physical disorders such as cerebral palsy, or a developmental delay that is considered too severe for participation
• Disorders of hemoglobin structure, function or synthesis
• Clinically significant nutritional deficiency requiring specialty nutritional therapy
• Any other clinically significant medical condition, which in the investigator's opinion, makes him or her unsuitable for inclusion in the study.

Where it is running

• Midway Medical Clinic — Oneonta, Alabama, United States
• HealthStar Research Glenwood — Glenwood, Arkansas, United States
• HealthStar Research, LLC — Hot Springs, Arkansas, United States
• L.A. Universal Research Center, Inc. — Los Angeles, California, United States
• Kissimmee Clinical Research — Kissimmee, Florida, United States
• Dade Research Center, LLC — Miami, Florida, United States
• D&H National Research Centers — Miami, Florida, United States
• Suncoast Research, Assoc., LLC — Miami, Florida, United States
• Springs Medical Research — Owensboro, Kentucky, United States
• Velocity Clinical Research — Covington, Louisiana, United States
• Southern Clinical Research — Zachary, Louisiana, United States
• Alivation Research (Primary Care) — Lincoln, Nebraska, United States
• Javara Inc. 3380 — Winston-Salem, North Carolina, United States
• Tribe Clinical Research LLC. — Greenville, South Carolina, United States
• Javara, Inc. 3377 — Dallas, Texas, United States
• Proactive Clinical Research — Edinburg, Texas, United States
• Gentle Pediatrics — Sugar Land, Texas, United States

Full record on ClinicalTrials.gov

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