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Recruiting NCT06855251

NCT06855251 SENSing Inner BodiLy State: Understanding the Role of Interoception in obEsity

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Clinical Trial Summary
NCT ID NCT06855251
Status Recruiting
Phase
Sponsor Istituto Auxologico Italiano
Condition Obesity
Study Type OBSERVATIONAL
Enrollment 32 participants
Start Date 2024-04-01
Primary Completion 2026-03-30

Eligibility & Interventions

Sex Female only
Min Age 18 Years
Max Age 55 Years
Study Type OBSERVATIONAL
Interventions
The crossmodal dual-task

Eligibility Fast-Check

Enter your details for a quick preliminary check. This does not replace medical advice.

What to Expect as a Participant

This is an observational study. You will not receive an experimental treatment; researchers will collect data based on your existing condition or standard treatment.

This trial targets 32 participants in total. It began in 2024-04-01 with a primary completion date of 2026-03-30.

⚠ This information is for research awareness only. Always consult your physician before joining any clinical trial. Participation is voluntary and you may withdraw at any time.

Brief Summary

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.

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

Contact & Investigator

Central Contact

Federica Scarpina, PhD

✉ f.scarpina@auxologico.it

📞 +39032351

Principal Investigator

Federica Scarpina, PhD

PRINCIPAL INVESTIGATOR

IRCCS Istituto Auxologico Italiano

Frequently Asked Questions

Who can join the NCT06855251 clinical trial?

This trial is open to female participants only, aged 18 Years or older, up to 55 Years, studying Obesity. Full inclusion and exclusion criteria are listed in the Eligibility Criteria section. Always confirm your eligibility with the research team before applying.

Is NCT06855251 currently recruiting?

Yes, NCT06855251 is actively recruiting participants. Contact the research team at f.scarpina@auxologico.it for enrollment information.

Where is the NCT06855251 trial being conducted?

This trial is being conducted at Piancavallo, Italy.

Who is sponsoring the NCT06855251 clinical trial?

NCT06855251 is sponsored by Istituto Auxologico Italiano. The principal investigator is Federica Scarpina, PhD at IRCCS Istituto Auxologico Italiano. The trial plans to enroll 32 participants.

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ClinicalMetric — Independent clinical trial intelligence platform. Not affiliated with NIH, ClinicalTrials.gov, the U.S. FDA, or any pharmaceutical company, hospital, or clinical research organization. Trial data is sourced from ClinicalTrials.gov for informational purposes only and does not constitute medical advice. Do not make any treatment, enrollment, or health decisions based solely on information found here — always consult a qualified healthcare professional. Full Disclaimer  ·  Last Reviewed: July 2026  ·  Data Methodology