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Behavioral and Neurofunctional Correlates of Intentional Motor Behaviors Towards Edible Stimuli in Normal-weight Subjects

Behavioral and Neurofunctional Correlates of Intentional Motor Behaviors Towards Edible Stimuli in Normal-weight Subjects

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04203706
Enrollment
48
Registered
2019-12-18
Start date
2020-02-01
Completion date
2023-01-31
Last updated
2019-12-18

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Food Oriented Behavior

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.

Interventions

OTHERNeurofunctional imaging

Subjects will be submitted to a functional neuroimaging scanning procedure

Sponsors

I.R.C.C.S Ospedale Galeazzi-Sant'Ambrogio
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
BASIC_SCIENCE
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to 80 Years
Healthy volunteers
Yes

Inclusion criteria

* Normal weight (Body mass index - BMI - comprised between 18.6 and 24.99. * 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/cm2. * Serious medical conditions, including but not limited to: hypertension, significant heart disease, disorders or illnesses that may compromise patient safety. * Pregnancy and Claustrophobia.

Design outcomes

Primary

MeasureTime frameDescription
BOLD Response3 yearsWe will record the BOLD response during the visualization of edible stimuli

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026