Skip to main content
OpenTrials
Completed

NCT Number: NCT02653378

The Effects of Acute Caloric Deprivation on Odour Identification and Food Reward

The purpose of this study is to determine how the modality of energy depletion can differently impact appetite hormones, ad libitum food intake, food hedonics, and olfaction.

Completed

Looking for future studies?

Notify Me

Key information

About this study

The objectives of the current randomized controlled study were to examine how the modality of an acute 3 day isocaloric -25% energy depletion by dieting alone or by aerobic exercise alone differently impacts appetite and appetite-related hormones, ad libitum energy intake (EI), food hedonics and food reward, and olfaction. It was hypothesized that independent of modality of depletion, that relative to the control, there would be increased ad libitum feeding and food reward, improvements in smell performance, and a decline in fasting leptin and increase in fasting total ghrelin. It was also hypothesized that the increased food reward would prove to be a predictor of ad libitum EI and that relative to the depletion by aerobic exercise alone, the depletion by diet alone would produce greater compensatory increases in appetite, ad libitum EI, and food reward.

Statistics

To test for differences in body weight, plasma hormone concentrations, relative-reinforcing value of food (RRVF), and olfaction across each condition of the study, repeated measures ANOVA controlling for day 1 as a covariate was employed. Pairwise comparisons at day 4 using Sidak adjustment to account for multiple comparisons are reported when the ANOVA was significant. One way repeated measures ANOVAs with Sidak adjustments for multiple comparisons were used to test for differences in variables measured only at day 4: body composition (fat mas, %Fat, and fat free mass), appetite, palatability, and ad libitum EI.

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Free from any illness that could influence outcome of the experiment
  • Weight-stable for >6months
  • aged between 18-40 years

Exclusion criteria

  • diabetic
  • smoker
  • medication

Treatment and study plan

Diet

Behavioral

25% Energy Depletion by Diet only for 3 Days

EX

Behavioral

25% Energy Depletion by Exercise only for 3 Days

Primary outcomes

  1. Change in Ad Libitum Energy Intake at Buffet Lunch--total kcals consumed at lunch meal measured to nearest 0.5grams.

    Time frame: Day 1 and Day 4 of each study arm (DIET and EX)

    Ad libitum measure of energy intake at lunch time at Day 1 and Day 4 of study

Secondary outcomes

  1. Change in fasting measure of Leptin

    Time frame: Day 1 and Day 4 of each study arm (DIET and EX)

    One fasting sample of plasma Leptin

  2. Change in fasting measure of Ghrelin

    Time frame: Day 1 and Day 4 of each study arm (DIET and EX)

    One fasting sample of plasma Ghrelin taken at Day 1 and Day 4 of study

  3. Change in Relative-Reinforcing Value of Food as measured by food points earned during a computerized behavioral choice tast

    Time frame: Day 1 and Day 4 of each study arm (DIET and EX)

    Computer task measuring reinforcing value of preferred snack food and preferred fruit at Day 1 and Day 4 of study

  4. Olfaction--Odor Detection Threshold measured by Sniffin Sticks odorized pens

    Time frame: Day 1 and Day 4 of each study arm (DIET and EX)

    Measure of odour threshold for n-butanol taken at Day 1 and Day 4 of study

Sponsors and collaborators

Lead sponsor

University of Ottawa

Other

Registry information

Acronym: DEXDER

Important dates

Study start
2009
Primary completion
2012
Study completion
2012
First posted
Jan 12, 2016
Registry last updated
Jan 12, 2016

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

Published trials that share one or more normalized conditions with this study.