About this trial
This prospective, double-blind, parallel-group controlled trial aims to investigate the consequence of early trauma on dopamine release evoked by positive valence odors.
Eligibility criteria
This trial accepts healthy volunteersQualifiers
Aged 18 years or older
Have been selected based on the Childhood Trauma Questionnaire score
Non-smoker
Be able to speak and read French
Disqualifiers
A pre-existing condition that affects olfaction including congenital anosmia, upper respiratory tract infection, nasal and/or sinus disease,
Be on medication, with the exception of oral contraceptives
Pregnant or breast-feeding woman (check with urine pregnancy tests);
Contraindications to TMS or MRI (implanted medical devices or metallic foreign body in the head);
Trial design
Parallel
Treatments tested in this trial
High score at Childhood Trauma Questionnaire.
Other interventionIn the "presence of early trauma" arm, 15 participants are recruited based on a high Childhood Trauma Questionnaire total score.
Low score at Childhood Trauma Questionnaire.
Other interventionIn the "absence of early trauma" arm, 15 participants are recruited based on a low Childhood Trauma Questionnaire total score.
Treatment groups
Trial outcomes
Primary outcomes
Dopamine transmission measured with positron emission tomography
Subcortical dopaminergic transmission will be analyzed, using \[11C\]raclopride PET activity (D2 receptor antagonist)
Secondary outcomes
Odor hedonic appreciation.
The pleasantness of the odors presented will be assessed on a scale of 1 to 9.
Functional brain connectivity.
Resting-state functional connectivity assessed with fMRI.
Effective brain connectivity
Effective brain connectivity will be assessed using a dual-coil TMS protocol that stimulates the motor cortex and dorsolateral prefrontal cortex during odor presentation. Measurement of the amplitude of the motor response reflects the connectivity between these two regions of interest.
Sponsors and contacts
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