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Specially Designed Eating Plates Effects on Food Intake in Normal Weight and Overweight Children

The Effect of Specially Designed Eating Plates on Self-served Portions and Caloric Intake in Normal Weight and Overweight Children

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02166892
Enrollment
22
Registered
2014-06-18
Start date
2014-07-01
Completion date
2017-12-01
Last updated
2018-03-22

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

Conditions

Obesity

Keywords

Childhood obesity, Plate, Food consumption

Brief summary

Previous studies demonstrated that children served themselves more food when using larger plates and bowels. The purpose of this study is to evaluate if self-served portions and caloric intake in normal weight and overweight children will be influenced by a specially designed eating plates compared to similar size normal plates.

Detailed description

40 normal weight and 40 overweight kindergarden and elementary school children will participate in this study. Anthropometric measurements: weight, height, BMI and BMI percentiles will be measured and calculated for each participant. The participants will take part in two non-exercise activities at the 'sport and health center for children and adolescence'. At the end of each activity, a lunch buffet that contains all food ingredients will be served. During one meeting the children will be handed a regular plate and at the second meeting they will be handed a specially designed plate (with marking of the recommended meal composition and portion). The amount and composition of food on the plates will be assessed by weighing and photography before and after eating and analysed to report macronutrient consumption by a dietitian. The meetings for normal weight children will be separated from the overweight children.

Interventions

OTHERSpecially designed plates

Sponsors

Dan Nemet, MD
Lead SponsorOTHER

Study design

Allocation
NON_RANDOMIZED
Intervention model
PARALLEL
Primary purpose
PREVENTION
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
4 Years to 13 Years
Healthy volunteers
Yes

Inclusion criteria

* Over weight / obese children * Normal weight children

Exclusion criteria

* Organic disease that cause obesity * Underweight children (BMI percentiles \< 5)

Design outcomes

Primary

MeasureTime frameDescription
Caloric intakeUp to 1 hour after food servingThe amount of food and drink consumed by the children will be evaluated.

Countries

Israel

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026