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Recruiting NCT06855251

SENSing Inner BodiLy State: Understanding the Role of Interoception in obEsity

Observational Obesity Body Representation

For patients and families

In plain language

An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.

What is being studied
The protocol lists: The crossmodal dual-task.
Who it may be relevant to
Registry conditions: Obesity, Body Representation. Basic parameters: 18 years — 55 years · Female.
What needs checking
Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
Where it takes place
Italy
Next step
Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →

Overview

Successfully perceiving the flow of interoceptive cues and integrating them with exteroceptive information are fundamental aspects of countering the body's inherent instability and guaranteeing homeostatic regulation. This process deeply affects cognitive/emotional functioning and general health. Recently, it has been suggested that an important signature underpinning obesity might be an interoceptive dysfunction in perceiving internal body signals and/or integrating them with information from the external environment. There is evidence that interoceptive deficits correlate with Body Mass Index (BMI), but it is still largely unclear how different measures and facets of interoception are related to high BMI and eating behaviour. Within this framework, it is mandatory to understand the role of interoception in obesity at perceptual, cognitive, and emotional levels. One open issue regards the relationships between interoceptive signals and the reactivity to external food cues.

Interventions

  • Behavioral The crossmodal dual-task
    Two main sensory tasks performed together: 1\. the visual task, in which participants are requested to monitor visual stimuli presented on a computer screen and to detect the "deviant" target" as soon as possible. The target changes across blocks: in half of the trials, participants will have to respond to food stimuli presented together with irrelevant non-food stimuli (food target condition); in the other half conditions, participants will have to respond to non-food stimuli presented togethe

Primary outcome measures

  • Visual detection velocity [Time frame: At the moment of the experiment]
  • Interoceptive judgement [Time frame: At the moment of the experiment]
Secondary outcome measures (1)
  • Visual detection accuracy [Time frame: At the moment of the experiment]

Eligibility criteria

Inclusion criteria

  • Right-handed individuals diagnosed with obesity
  • In rehabilitative treatment at the Istituto Auxologico

Exclusion criteria

  • Concurrent neurological, neurodevelopmental (e.g., autism), motor, somatosensory and/or psychiatric disorders

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: Yes

Study design

Observational model
Case-control

Study locations

Italy · 1 center
  • IRCCS Istituto Auxologico Italiano - Ospedale San Giuseppe — Piancavallo

Identifiers

NCT: NCT06855251 · 21C404

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗