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CompletedNCT01720589MeltUpdated May 30, 2013

Effect of Dietary Fat Cooking Blend on Energy Expenditure in Children

An interventional study of Melt (test oil) and Corn oil (control) in Childhood Obesity, sponsored by St. Luke's-Roosevelt Hospital Center. Completed at 1 site in United States. Open to participants aged 15 Years to 18 Years, including healthy volunteers. Per ClinicalTrials.gov, last updated 2013-05-30.

Sponsored by St. Luke's-Roosevelt Hospital Center · Not applicable, Interventional, and Prevention

Phase
Not applicable
Study type
Interventional
Enrollment
5
Allocation
Randomized
Ages
15 Years to 18 Years
Sex
All
01

Study summary

The purpose of this study is to test the effects of a cooking oil blend of dietary fats rich in medium chain triglycerides on energy expenditure and food intake in overweight and obese children.

02

Conditions studied

  • Childhood Obesity

Keywords

  • Obesity
  • Dietary fat
  • Energy expenditure
  • Food intake
03

In context

Obesity

6,296 studies on the registry are indexed under Obesity; 1,695 are open to participants now.

This study's enrollment of 5 is below the median of 78 across 4,878 interventional studies indexed under Obesity.

Browse Obesity studies →

Lead sponsor

St. Luke's-Roosevelt Hospital Center is the lead sponsor of 68 studies on the registry; none are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
15 Years to 18 Years
Sexes eligible
All
Accepts healthy volunteers
Yes

Inclusion criteria

  • age 15-18
  • body mass index 85% percentile or higher for age/sex
  • weight stable

Exclusion criteria

Exclusion Criteria:

  • ±5 lbs weight change in the the 3 months prior
  • use of medications
  • dietary allergies
  • metabolic disorder
  • eating disorder
  • behavioral or psychological disorders
05

Study design

Phase
Not applicable
Primary purpose
Prevention
Allocation
Randomized
Intervention model
Crossover assignment
Masking
Double (Participant, Investigator)
Enrollment
5 participants (actual)

Study arms

  • Experimental
    Melt (test oil)

    Participants will consume a muffin containing 20 g of dietary fat provided by the test oil and their energy expenditure will be measure post-prandially for 6 hours. At the end of the measurement period, participants will consume a cookie containing 10 g of fat provided by the test oil and their food intake at an ad libitum meal will be measured 1 hour later.

    Dietary Supplement: Melt (test oil)

  • Active comparator
    Corn oil (control)

    Participants will consume a muffin containing 20 g of dietary fat provided by the control oil and their energy expenditure will be measure post-prandially for 6 hours. At the end of the measurement period, participants will consume a cookie containing 10 g of fat provided by the control oil and their food intake at an ad libitum meal will be measured 1 hour later.

    Dietary Supplement: Corn oil (control)

Interventions

  • Dietary supplementMelt (test oil)
  • Dietary supplementCorn oil (control)
06

What researchers measure

Primary outcomes

  1. Thermic effect of food

    Measurement of thermic effect of food over 6 hours after a meal rich in test oil and control oil. The thermic effect of food is the difference between post-prandial energy expenditure and basal energy expenditure. We will assess the difference in thermic effect of food over a 6-hour period between the test oil and the control oil.

    Time frame: 6 h

  2. Respiratory quotient/fat oxidation

    Measurement of substrate oxidation by indirect calorimetry over 6 hours after consumption of the test oil and control oil. We will specifically calculate carbohydrate and fat oxidation rates over the 6-hour period post-prandially and compare rates of oxidation of these two substrates between the test oil and the control oil.

    Time frame: 6 h

  3. Food intake

    Measurement of food intake at a single meal served 1 hour after a pre-load containing 8-10 g of the test oil and the control oil

    Time frame: single meal

Secondary outcomes

  1. Glucose

    Measurement of glucose over 6 hours after consumption of the test oil and control oil

    Time frame: 6 h

  2. Feelings of appetite and satiety

    Measurement of feelings of appetite and satiety by visual analog scales over 6 hours after consumption of the test oil and control oil

    Time frame: 6 h

  3. Insulin

    Measurement of insulin over 6 hours after consumption of the test oil and control oil

    Time frame: 6 hours

  4. Leptin

    Measurement of leptin over 6 hours after consumption of the test oil and control oil

    Time frame: 6 hours

  5. Ghrelin

    Measurement of ghrelin over 6 hours after consumption of the test oil and control oil

    Time frame: 6 hours

  6. Peptide YY

    Measurement of peptide YY over 6 hours after consumption of the test oil and control oil

    Time frame: 6 hours

  7. Glucagon like peptide 1

    Measurement of glucagon like peptide 1 over 6 hours after consumption of the test oil and control oil

    Time frame: 6 hours

07

Study locations

1 site
  • St. Luke's/Roosevelt Hospital
    New York, New York 10025, United States
08

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on May 30, 2013, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
09

Registry details

Key details

Study ID
NCT01720589
Lead sponsor
St. Luke's-Roosevelt Hospital Center
Collaborators
Prosperity Organic Foods, USDA Beltsville Human Nutrition Research Center
Responsible party
Marie-Pierre St-Onge (Research Associate, St. Luke's-Roosevelt Hospital Center) — Principal investigator
First posted
Nov 2, 2012
Start date
Oct 2012
Primary completion
Feb 2013
Completion
Feb 2013
Last update
May 30, 2013

Study contacts

Marie-Pierre St-Onge, Ph.D
principal investigator · St. Luke's-Roosevelt Hospital Center
Cygnia Rapp
principal investigator · Prosperity Organic Foods

Oversight

Data monitoring committee
Yes
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is completed, as verified in May 2013. You cannot join it, but the record below documents what was studied.

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