- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT03095833
Food Intake Decisions
Food Decisions and Reward System: Modulation by Olfaction and Taste
Study Overview
Status
Conditions
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
-
-
-
Bron, France, 69500
- CH Le Vinatier
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Description
Inclusion Criteria:
- healthy or Prader-Willi
- right handed
Exclusion Criteria:
- Nursing or pregnant women
- undergoing medical treatment
- Having known olfactory disorder
- neurological or psychiatric history
- all pertinent conditions according to the use of magnetic resonance imaging.
- anosmia (partial/total)
- neurological, psychological or other disease
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Basic Science
- Allocation: Non-Randomized
- Interventional Model: Parallel Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Other: Influence of cognitive biases on food intake
Determine how high-level cognitive control can affect the price to pay for a food and the olfactory and visual perception of these foods in healthy subjects and Prader-Willi patients.
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Four odors are available: "milk chocolate", "dark chocolate", "pineapple" and "apricot". In addition, a neutral odor will be used "clean air", a control odor transmitted during the task by the olfactometer in the same way as the other 4 odors, the only variant being that no odor will be deposited in the U-tube containing the smells. The images corresponding to the odors will be displayed after the odor has been proposed.
Concerning behavioral passes, the subjects will be in front of a computer screen on which the task will be presented.
For fMRI passes, the visual stimulation of the participant is done by a mirror system placed about 10 cm from the participant's eyes, allowing him to watch a translucent screen on which the visual stimuli are projected.
The latter have an intensity similar to that of television images, and therefore below the maximum permitted by labor legislation.
The stimuli will be projected via a video projector located at the back of the imager.
The olfactory sensitivity and the olfactory identification capacities of the subjects will be evaluated using the ETOC test.
Subjects will have to define his state of hunger/satiety thanks to a questionnaire of hunger.
Finally, subjects should assess the hedonic nature of the odor and the edibility of the odor source.
The task to be performed will be the same for the behavioral study as for the imaging study.
The subject will receive instruction from the following three: "indulge yourself", the subject must think of the desire to eat the food that will be presented to him in olfactory and visual form; "Be natural," the subject must act as naturally as possible; Or "hold back," the subject must distance themselves from their desire to eat and control themselves.
In a second step, an odor will be presented for 5 seconds.
This will be based on the subject's inspiration, then an image associated with the odor will be presented for two seconds.
Before and after the imaging examination, a blood sample will be taken by a medical imaging manipulator affiliated with the CERMEP whose actions will be remunerated in accordance with the usual hygiene and safety rules.
The samples taken will then be annotated with the subject code and kept at the CERMEP.
The volume of ghrelin sampling is 5 ml (10 ml for two samples).
The volume of the leptin is 5 ml (ie 10 ml for two samples).
The proposed questionnaires respond to all ethical aspects established by international and national standards to undertake studies on human subjects.
Two types of questionnaires will be used in this experiment: Inclusion of the Subjects and Exploratory Tests.
The purpose of the imaging part is to determine how high-level cognitive control (the setpoint) can affect the price of a food and the olfactory and visual perception of these foods in healthy subjects and Prader-Willi patients.
|
|
Other: Modulation of the floral flavor of a wine
Highlight the brain regions involved in the visual bias related to the intensity of a wine's dress combined with the floral character evaluation of its flavor.
|
Before and after the imaging examination, a blood sample will be taken by a medical imaging manipulator affiliated with the CERMEP whose actions will be remunerated in accordance with the usual hygiene and safety rules.
The samples taken will then be annotated with the subject code and kept at the CERMEP.
The volume of ghrelin sampling is 5 ml (10 ml for two samples).
The volume of the leptin is 5 ml (ie 10 ml for two samples).
The proposed questionnaires respond to all ethical aspects established by international and national standards to undertake studies on human subjects.
Two types of questionnaires will be used in this experiment: Inclusion of the Subjects and Exploratory Tests.
The purpose of the imaging part is to determine how high-level cognitive control (the setpoint) can affect the price of a food and the olfactory and visual perception of these foods in healthy subjects and Prader-Willi patients.
To modify the floral character of the wine used, the investigators will use the β-ionone odorant molecule (4 (2,6,6-trimethyl-1-cyclohexenyl) -3-buten-2-one (CAS number 14901-07-6) Purity ≥97.0%
(Fluka) This molecule is commonly found in wines with a violet odor.
The visual stimulation of the subject will be done by a system of mirrors placed about 10 cm from the subject's eyes allows him to look at a translucent screen behind the MRI scanner and on which the visual stimuli are projected.
For each test the subjects will receive at the same time an image on the screen and a sample of wine (2 ml) delivered in the mouth of the subject thanks to the system of programmable pumps.
Sampling will be done by the subject himself by scratching and firmly pressing into the oral cavity, specifically at the cheeks and tongue for one minute, being careful not to touch the teeth and gums.
The investigators will determine how perceptual judgments are modulated by cross-modal stimuli, as well as metacognitive judgments (how individuals judge their own sensory performance).
In addition, they will determine how perceptual judgments are modified in the context of group decisions and how language influences performance.
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
brain activity related to the perception of food odors and flavor
Time Frame: Hour 1
|
functional magnetic resonance imaging data
|
Hour 1
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
behavioral ratings of odor/flavor valuation by participants
Time Frame: Hour 1
|
behavioral ratings of odor/flavor valuation by participants
|
Hour 1
|
|
blood alcohol level post experiment
Time Frame: 10 minutes
|
reference value for file information
|
10 minutes
|
Collaborators and Investigators
Sponsor
Investigators
- Principal Investigator: Caroline DEMILY, MD, CH Le Vinatier
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Other Study ID Numbers
- 69HCL16_0681
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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