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Clinical Trial Details — Status: Not yet recruiting

Administrative data

NCT number NCT04916652
Other study ID # 20.02.INF
Secondary ID
Status Not yet recruiting
Phase
First received
Last updated
Start date November 2023
Est. completion date March 2025

Study information

Verified date October 2023
Source Société des Produits Nestlé (SPN)
Contact Joyce Li
Phone +86 15810125435
Email joyce.li@rd.nestle.com
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

The overall objective is to characterize the developmental characteristics of MRI measured neural flexibility, as an index of cognitive flexibility, in Chinese toddlers (32 to 42 months old).


Description:

The primary objective of this clinical study is to characterize in Chinese toddlers ages 32 - 42 months old the developmental characteristics of MRI measured neural flexibility, as an index of cognitive flexibility, and to assess a range of executive functions (inhibit, shift, emotional control, working memory, plan/organize) using the Global Executive Composite summary score obtained from the BRIEF-P standardized rating scale.


Recruitment information / eligibility

Status Not yet recruiting
Enrollment 60
Est. completion date March 2025
Est. primary completion date February 2025
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 32 Months to 34 Months
Eligibility Inclusion Criteria: 1. Written informed consent has been obtained from the parent/legally acceptable representative. 2. Full-term birth (more than 37 weeks and >2.5kg) 3. Children aged between 32 to 34 mo or 2.8 to 2.10 years at enrollment 4. Neurotypical development as assessed by interview 5. No major risk factors for learning, neurologic, or psychiatric disorder as assessed by interview [defined as a diagnosed learning neurologic or psychiatric disorder in a first degree relative (e.g. parents, siblings)]. 6. Dietary requirement detailed below: S-26 GOLD or ULTIMA GUM--fed group: I. Daily consumption of S-26 GOLD or ULTIMA GUM for the last 60 days (2 months) II. Desire of the parent to continue feeding GUM during the course of the study Cow's milk-fed group: I. Daily consumption of cow's milk or for the last 60 days (2 months) II. Desire of the parent to continue feeding cow's milk during the course of the study Exclusion Criteria: 1. Delayed birth ( > 41 weeks gestation) as reported in medical record 2. Birth Weight < 2500 g or small for gestational age (birth weight below the 10th percentile) or large for gestational age (birth weight above the 90th percentile) as reported in medical record 3. History of neurological (e.g., head injury, epilepsy), psychiatric or developmental disorder in the toddler as assessed by interview 4. History of diagnosed neurological (e.g., head injury, epilepsy), psychiatric or developmental disorder in parents or siblings, as assessed by interview 5. In utero exposure to alcohol abuse or illicit substances as defined as diagnosis of current substance use disorder in the biological mother and guidelines set by the American College of Obstetricians and Gynecologists and the Royal College of Physicians 6. Multiple birth as reported in medical record 7. Complicated pregnancy (e.g., preeclampsia, gestational diabetes) as assessed by medical interview/ medical record 8. Abnormal screening laboratory values and studies considered to be clinically significant in the opinion of the Investigator (e.g., metabolic disease screening, neonatal bilirubin)

Study Design


Related Conditions & MeSH terms


Intervention

Radiation:
MRI
MRI is a safe, non-invasive, cutting edge imaging technology widely used to study the human brain both internationally (NIH connectome project) and in China (China Brain Project). The Baby Connectome Project (BCP) led by NIH scientists has begun data collection on the structural and functional brain development among American infants (Howell, Styner et al. 2019).

Locations

Country Name City State
China Shanghai Children's Medical Center Shanghai Shanghai

Sponsors (3)

Lead Sponsor Collaborator
Société des Produits Nestlé (SPN) SAS Institute, Veeva Systems

Country where clinical trial is conducted

China, 

Outcome

Type Measure Description Time frame Safety issue
Other Anthropometry (weight in grams) Weight in grams and corresponding weight-for-age Z-score according to the WHO growth standards at baseline and 8 month after baseline
Other Anthropometry (body length in centimeters) Length in centimeters and corresponding length-for-age Z-score according to the WHO growth standards at baseline and 8 month after baseline
Other Anthropometry (weight-for-length) Corresponding weight-for-length Z-score according to the WHO growth standards at baseline and 8 month after baseline
Other Anthropometry (head circumference in centimeters) Head circumference in centimeters and corresponding head-circumference-for-age Z-score according to the WHO growth standards at baseline and 8 month after baseline
Other Anthropometry (BMI) Weight and height will be combined to report the BMI (kg/m2) and corresponding BMI-for-age Z-score according to the WHO growth standards at baseline and 8 month after baseline
Other Gastrointestinal tolerance (for infants) using validated Infant Gastrointestinal Symptom Questionnaire (IGSQ) for age 1.5-12 months at baseline and 8 month after baseline
Other Gastrointestinal tolerance (for toddlers) using the Toddler Gut Comfort Questionnaire (TGCQ) for age 12-24 months at baseline and 8 month after baseline
Other Adverse Events (e.g., type, incidence, severity, seriousness) standard AE reporting procedure from enrollment until 36 months of age
Primary Neural flexibility Neural flexibility is a quantitative measure of the frequency at which brain regions change their allegiance from one functional module to another during a given time period. It will be measured by MRI at the brain regions implicated to be associated with cognitive flexibility (including anterior cingulate cortex, dorsolateral prefrontal cortex, ventrolateral prefrontal cortex, anterior insula, interior frontal junction, superior parietal lobule, precuneus, intraparietal sulcus, frontal eye fields, and temporoparietal junction) at baseline and 8 months after baseline
Secondary Brain structure (brain regions volume) Brain structure (brain regions volume) measured using MRI, including the hippocampal and frontal lobe volume (in cubic millimeter) at baseline and 8 months after baseline
Secondary Brain structure (cortical surface area) Brain structure (cortical surface area) measured using MRI at baseline and 8 months after baseline
Secondary Brain structure (cortical thickness) Brain structure (cortical thickness) measured using MRI at baseline and 8 months after baseline
Secondary Brain structure (myelination) Brain structure (myelination) measured using MRI at baseline and 8 months after baseline
Secondary Brain function (network topologies) Brain functional network topologies of the nine commonly assessed brain functional networks, including the primary visual, secondary visual, visual association, motosensory, default mode, frontoparietal, medial frontal, subcortical and cerebellum networks using MRI at baseline and 8 months after baseline
Secondary Brain function (connection strengths) Brain functional connection strengths of the nine commonly assessed brain functional networks, including the primary visual, secondary visual, visual association, motosensory, default mode, frontoparietal, medial frontal, subcortical and cerebellum networks using MRI at baseline and 8 months after baseline
Secondary Children development Using the Griffiths Mental Development Scales for China (GDS-C). Gross and fine motor, personal-social-emotional, language and communication and learning development will be assessed at baseline and 8 months after baseline
Secondary Children attention Using an established eye tracking protocol in Chinese pediatric population (using the Tobii TX300 eye tracker) at baseline and 8 months after baseline
Secondary Children behavior (for infants) Using the Infant Behavior Questionnaire (IBQ) for age 3-12 months at baseline and 8 months after baseline
Secondary Children behavior (for toddlers) Using the Early Childhood Behavioral Questionnaire (ECBQ) for age 13 - 36 months at baseline and 8 months after baseline
Secondary Sleep quality Sleep quality, duration and efficiency (total sleep time / duration of sleep episode *100) computed using the Brief Infant Sleep Questionnaire (BISQ). In addition, an actigraphy in combination with a sleep diary will be used during home period and their relationship will indicate the sleep quality at baseline and 8 months after baseline
Secondary Fecal microbiota composition Measured via the shotgun metagenomics sequencing for species composition and functional pathways through stool samples collected at baseline and 8 months after baseline
Secondary Breast milk composition Breast milk composition (lipids, carbohydrates, proteins, minerals and vitamins) will be measured by the MIRIS analyzer through breast milk samples collected (only for breast-fed subjects) at baseline and 8 months after baseline
Secondary Feeding practice Using validated Child Feeding Practice Questionnaire. In addition, to complete the feeding and adverse events calendar monthly during home period at baseline and 8 months after baseline
Secondary Home environment Using Home Environment questionnaire to collect information on household: siblings, and whether parents receive help on feeding the child. at baseline and 8 months after baseline
Secondary Cognitive flexibility Using the Behavior Rating Inventory of Executive Function-Preschool Version (BRIEF-P) and the Dimensional Change Card Sort (DCCS) task at 36 months of age
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