Impact of Fatty Stimuli on Cerebral Activity in Anorexia Nervosa: a Multi-sensory Approach

Trial statusNot yet recruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexFemale
Age18+
SponsorCentre Hospitalier Universitaire de Saint Etienne

About this trial

Lipid restriction is significant in anorexia nervosa and limits therapeutic management. The multisensory perception of fat is altered, creating an aversion to lipids. The investigators aim to characterize the impact of sensory stimulation (smells or images) associated with specific tastes using neuropsychological assessments and functional MRI. Some volatile aromas can enhance the perception of the associated taste. The investigators hypothesize that such associations are altered in anorexia nervosa for fatty foods but may be preserved for sweet tastes, and that this alteration contributes to the maintenance of the disease. The interdependence of different sensory perceptions of lipids could play a major role in the therapeutic approach, aiding in the deconditioning of this aversion and the restoration of positive food sensory associations.

Eligibility criteria

This trial accepts healthy volunteers

Qualifiers

Person affiliated or entitled to a social security scheme

Person having received informed information on the study and having co-signed, with the investigator, a consent to participate in the study

female person

Person affiliated or entitled to a social security scheme

Disqualifiers

Pregnant women, parturient, nursing mothers;

Persons deprived of their liberty, hospitalized without consent, hospitalized for purposes other than research;

Minors

Refusal of the study by the participant

Trial design

Design model

Parallel

Treatments tested in this trial

  • MRI examination

    Other intervention

    One hour MRI examination

  • Smell and taste capacity testings

    Other intervention

    one hour sensory testings

Treatment groups

90 Participants
are divided into 3 treatment groups
Group A: Anorexia Nervosa patient groupExperimental treatment 2 interventions
Group B: Normal Weight Control groupActive comparator 2 interventions
Group C: Low Weight Control groupActive comparator 2 interventions

Trial outcomes

Primary outcomes

1

Brain activity measured by functional MRI

Estimation of the "fatty vs. neutral" contrast when all three senses are used, comparing AN patients to the normal-weight control group (NC group) in each voxel of the brain volume (whole-brain analysis) and in the orbitofrontal cortex (ROI analysis).

Time frame
Day 1

Secondary outcomes

1

Brain activity measured by functional MRI

Estimation of the "fatty vs. neutral" contrast when all three senses are used, comparing AN patients to the control group with a similar BMI (CT group) in each voxel of the brain volume (whole-brain analysis) and in the orbitofrontal cortex (ROI analysis).

Time frame
Day 1
2

Brain activity measured by functional MRI

BOLD signal variations between the groups (AN, NC, and CT) for the "sweet vs. neutral" contrast.

Time frame
Day 1
3

Brain activity measured by functional MRI

BOLD signal variations for single vs. three senses simultaneously for each group and between groups for the "fatty vs. neutral" and "sweet vs. neutral" contrasts.

Time frame
Day 1
4

BMI

Body Mass Index

Time frame
DAY 1.

Other outcomes

Sponsors and contacts

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