Hed-O-Shift: Hedonic and Neurocognitive Processes in Relation to Dietary Habits and Weight Status

Rennes University Hospital

Status: Completed

Conditions: Neurocognitive Correlates of Eating Habits

Treatments: Other: First Visit; Other: on-line questionnaires; Device: fMRI

Study type: Interventional

Funder types: Other

Identifiers

NCT03076489

35RC17_9740_Hed-O-Shift

Details and patient eligibility

About

This study includes an inclusion visit, 2 visits to the Rennes University Hospital and the filling of two on-line questionnaires.

The first visit to the University-Hospital of Rennes, during which a blood sample will be taken, morpho-anatomic measures (height, weight, hip and size), impedancemetry and resting energy expenditure by indirect calorimetry will be carried out in the Clinical Investigation Unit.

During this visit, the volunteers will also have to bring a sample of urine and faeces previously collected at home.

The two on-line questionnaires (hedonic and caloric evaluation of foods and beverages on photos) will have to be completed by the volunteers between the first and the second visit to the University-Hospital.

Finally, the volunteers will go to the University-Hospital of Rennes for the second visit, on the Neurinfo platform, during which they will be subjected to a cognitive two-choice test based on food and drink pictures, during fMRI. Before and after the fMRI session, an assessment of the state of hunger, thirst, and general status of the volunteer will be carried out using a numerical scale ranging from 1 to 10.

Enrollment: 50 patients

Sex: Female

Ages: 18 to 24 years old

Volunteers: Accepts Healthy Volunteers

Inclusion criteria

• Women aged 18-24,
• Presenting a normal BMI (18-25),
• Right-handers,
• Affiliated to a social security scheme
• Having given a free, informed and written consent.
• Having a low frequency of consumption of fatty and / or sugary / salty foods, or on the contrary, a high frequency of consumption of these foods.

Exclusion criteria

• Related to the study:
• High level athletes, (determined on the basis of the Ricci & Gagnon questionnaire - excluded if score > 32);
• Food abstinents for religious, ideological or health reasons (intolerance, vegetarianism, allergies, etc.);
• Family history of obesity or diabetes;
• Personal history of TCA, anxiety or depressive disorder, or proven addictive behaviour;
• Excessive consumption of alcohol or other psychoactive substances (determined on the basis of the AUDIT questionnaires - excluded if score > 7 and CRAFT - excluded if score> 2 " yes ");
• Smoking daily or having stopped for less than 6 months;
• History of bariatric surgery;
• On-going treatment in the nutrition unit;
• Insufficient command of French;
• Pregnant or nursing women;
• Persons of full age who are subject to legal protection (safeguard of justice, curatorship, guardianship), persons deprived of their liberty.
• Simultaneous participation in another research protocol involving the human person

Related to fMRI:

• Implantable cardiac pacemaker or defibrillator;
• Neurosurgical clips;
• Cochlear implants;
• Neural or peripheral stimulator;
• Foreign orbital or brain metallic foreign bodies;
• Endoprostheses implanted for less than 4 weeks and osteosynthesis materials placed for less than 6 weeks;
• Claustrophobia.

Trial design

Primary purpose: Other

Allocation: Non-Randomized

Interventional model: Parallel Assignment

Masking: None (Open label)

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50 participants in 2 patient groups

high consumption habits

Experimental group

Description:

high consumption habits of fatty and sugary foods

Treatment:

Other: on-line questionnaires

Other: First Visit

Device: fMRI

low consumption habits

Experimental group

Description:

low consumption habits of fatty and sugary foods

Treatment:

Other: on-line questionnaires

Other: First Visit

Device: fMRI