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Clinical Trials in Israel / NCT07808983
Recruiting Not applicable

Chewing, Eating Rate, and Weight Status in Children

NCT07808983 · tracked via the Priya Life Science Israel tracker
Phase
Not applicable
Started
2026-09-01
Last updated
2026-09-09

Condition(s) studied

Healhty

Investigational drug(s) / intervention(s)

Test meal BTest meal A

Test meal B: A standardized Mediterranean-style breakfast consisting of bread, a thin omelet, grated carrot, sliced cucumber, apple purée, and a banana.

Test meal A: A typical Medittarenean breakfast with a soft texture including: Bread, flat omlet, grated carot, sliced cucamber, apple puree and a banana

Study summary

Background: Childhood obesity is a multifactorial health condition associated with profound metabolic, psychosocial, and socioeconomic ramifications across the lifespan. Among eating behaviors associated with obesity, limited attention has been given to chewing and food texture as pathways that may influence energy intake and weight regulation. Existing pediatric research remains scarce, methodologically heterogeneous, and often inconclusive.

Aims: This study aims to examine associations between oral processing behaviors during a standardized meal, including eating duration, eating rate, Ghrelin levels, and anthropometric measures in healthy children.

Methods: Participants responding to public advertisements will be screened for eligibility, including age (6-11 years), health status, absence of food allergies or intolerances, dental or developmental problems, and measured weight and height to achieve a sample of 40 children with obesity and 40 with normal weight. In a randomized crossover design, participants will consume two isocaloric, non-processed test meals differing in food texture (soft vs. hard) during separate laboratory visits. Eating behavior will be objectively assessed using a Universal Eating Monitor with synchronized video analysis to quantify chewing time, number of chews, and eating rate. Salivary ghrelin, subjective satiety (measured using visual analog scales), and total daily energy intake (assessed via 24-hour dietary recall) will be evaluated, along with anthropometric, body composition, strength measures, and sociodemographic and behavioral data. To account for familial and shared environmental influences on eating behavior, at least one parent will undergo a parallel assessment, conducted separately from the participating child. Participants will receive a modest shopping voucher to facilitate retention. Associations between oral processing behaviors, physiological responses, and weight status will be examined using multivariable regression models. Exploratory mediation analyses will be conducted to assess whether ghrelin and satiety responses partially account for the observed associations.

Eligibility

Sex
ALL
Min age
6 Years
Max age
11 Years
Healthy volunteers
Accepted
Inclusion Criteria: * Healthy children aged 6-11 years and their parents who are fluent in Hebrew or English. Exclusion Criteria: * Children with dietary restrictions due to medical indications, such as celiac disease, inflammatory bowel disease, or other health conditions that may affect their ability to accept identical test meals included in the research. * Children who are treated with medications for ADD or ADHD. * Children with recent tooth loss or an oral injury that interferes with their ability to chew or eat normally at the time of assessment.

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
Ariel University Ariel Israel Recruiting

More Ariel University trials in Israel

Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT07808983 on ClinicalTrials.gov ↗ ← All trials in Israel