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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT02166892
Other study ID # MeirMc0042-14CTIL
Secondary ID
Status Completed
Phase N/A
First received June 9, 2014
Last updated March 21, 2018
Start date July 1, 2014
Est. completion date December 1, 2017

Study information

Verified date March 2018
Source Meir Medical Center
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial 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.


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.


Recruitment information / eligibility

Status Completed
Enrollment 22
Est. completion date December 1, 2017
Est. primary completion date December 1, 2017
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 4 Years to 13 Years
Eligibility Inclusion Criteria:

- Over weight / obese children

- Normal weight children

Exclusion Criteria:

- Organic disease that cause obesity

- Underweight children (BMI percentiles < 5)

Study Design


Related Conditions & MeSH terms


Intervention

Other:
Specially designed plates


Locations

Country Name City State
Israel Meir Medical Center Kfar Saba

Sponsors (1)

Lead Sponsor Collaborator
Dan Nemet, MD

Country where clinical trial is conducted

Israel, 

Outcome

Type Measure Description Time frame Safety issue
Primary Caloric intake The amount of food and drink consumed by the children will be evaluated. Up to 1 hour after food serving
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