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Clinical Trials/NCT04203706
NCT04203706
Unknown
N/A

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 enrollmentFebruary 1, 2020

Overview

Phase
N/A
Intervention
Not specified
Conditions
Food Oriented Behavior
Sponsor
I.R.C.C.S Ospedale Galeazzi-Sant'Ambrogio
Enrollment
48
Primary Endpoint
BOLD Response
Last Updated
6 years ago

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.

Registry
clinicaltrials.gov
Start Date
February 1, 2020
End Date
January 31, 2023
Last Updated
6 years ago
Study Type
Interventional
Study Design
Single Group
Sex
All

Investigators

Sponsor
I.R.C.C.S Ospedale Galeazzi-Sant'Ambrogio
Responsible Party
Sponsor

Eligibility Criteria

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

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