NCT04203706UnknownNot Applicable
Behavioral and Neurofunctional Correlates of Intentional Motor Behaviors Towards Edible Stimuli in Normal-weight Subjects
I.R.C.C.S Ospedale Galeazzi-Sant'Ambrogio0 sites48 target enrollmentStarted: February 1, 2020Last updated:
Conditions
Trial Snapshot
- Phase
- Not Applicable
- Sponsor
- Enrollment
- 48
- Primary Endpoint
- BOLD Response
Study Overview
Brief Summary
This study aims to investigate, through behavioural tests combined with advanced neurofunctional methods, the neural bases of intentional behaviours towards edible stimuli using explicit and implicit paradigms in normal-weight subjects.
This knowledge will then be expanded with the study of associations between behavioral/neurofunctional measures and blood/hummon parameters.
Study Design
- Study Type
- Interventional
- Allocation
- Na
- Intervention Model
- Single Group
- Primary Purpose
- Basic Science
- Masking
- None
Eligibility Criteria
- Ages
- 18 Years to 80 Years (Adult, Older Adult)
- Sex
- All
- Accepts Healthy Volunteers
- Yes
Inclusion Criteria
- •Normal weight (Body mass index - BMI - comprised between 18.6 and 24.
- •Absence of usual contraindications to MRI examination (e.g. pacemakers, fixed hearing implants, presence of metallic foreign bodies, intrauterine bodies, metallic splinters or fragments, metallic prostheses, screws, nails, fixed or mobile dental prostheses).
- •Signature of informed consent and consent to cooperate in all study procedures.
Exclusion Criteria
- •Previous diagnosis of significant neurological disorders (brain damage or dementia), major psychiatric disorders or eating disorders (binge-eating disorder, bulimia).
- •BMI less than 18.5 and greater than or equal to 25 Kg/cm
- •Serious medical conditions, including but not limited to: hypertension, significant heart disease, disorders or illnesses that may compromise patient safety.
- •Pregnancy and Claustrophobia.
Outcomes
Primary Outcomes
BOLD Response
Time Frame: 3 years
We will record the BOLD response during the visualization of edible stimuli
Secondary Outcomes
No secondary outcomes reported
Investigators
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