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Visuo-Tactile Integration and Body Ownership in the Human Brain

Visuo-Tactile Integration and Body Ownership in the Human Brain

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05164991
Enrollment
45
Registered
2021-12-21
Start date
2022-01-10
Completion date
2023-09-12
Last updated
2023-09-13

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

Conditions

Behavior and Behavior Mechanisms, Body Representation

Brief summary

The present project exploits brain imaging and neuroscience robotics to investigate the role of quantifiable visual input on the relationship between visuo-tactile integration and body ownership (the feeling that this body belongs to me).

Detailed description

Observational study, fundamental research, multicentric, national. The analysis of questionnaires, self-reports, and brain imaging associated with the RHI is used to understand the influence of visual input on body ownership. To this aim, participants lay down in the magnetic resonance (MR) scanner (Figure 1B), are presented with visual stimuli (videos of the virtual rubber hand - visual stroking) simultaneously in real time with tactile stimuli (robotic stroking of the participant's hand - tactile stroking), and in combination or not with the measurement of autonomic arousal (GSR) associated with the observation of a video showing the virtual rubber hand in a threatening situation (e.g. a knife approaching the virtual hand - unconscious RHI effects). By means of structured questionnaires and semi-structured self-reports, participants (i) evaluate eventual sensations felt during the visuo-tactile stimulation and (ii) report the personal feelings and impressions about body ownership for the virtual rubber hand (conscious RHI effects).

Interventions

BEHAVIORALVisuo-tactile stimulations of the right hand

Participants lay down in the magnetic resonance (MR) scanner are presented with visual stimuli (videos of the virtual rubber hand - visual stroking) simultaneously in real time with tactile stimuli (robotic stroking of the participant's hand - tactile stroking). An MR-compatible robot systematically provides the tactile stroking on the participant's hand. MR-compatible goggles show the visual stroking. Patterns of long and short robotic movements will be provided.

Sponsors

Psychiatric University Hospital, Zurich
CollaboratorOTHER
Eye Hospital Jules Gonin
CollaboratorOTHER
Swiss Federal Institute of Technology
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
BASIC_SCIENCE
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to 55 Years
Healthy volunteers
Yes

Inclusion criteria

* general health * personal interest * age between 18 and 55 years old * fulfil standard guidelines for fMRI studies

Exclusion criteria

* history of seizures, epilepsy * specific medications or treatment * concomitant diseases (e.g. cardiopathy) * pregnancy * unexplained loss of consciousness * chronic headaches * neurological illnesses * head concussion, * presence of metal in the neck or head * implanted medical devices * drug abuse * inability to give consent

Design outcomes

Primary

MeasureTime frameDescription
Neuro-behavioral changes associated with vision-dependent alterations of body ownership, measured via brain activity (fMRI)Through study completion, an average of 2 yearsAnalysis of objective measures of the RHI

Secondary

MeasureTime frameDescription
Subjective Experience via VAS scaleThrough study completion, an average of 2 yearsTo understand the variations of the body ownership, Visual Analogic Scale, values 0 to 7, 0 = no illusory body ownership, 7 = strong illusory body ownership
Automatic response (skin conductance)Through study completion, an average of 2 yearsMeasure of the skin conductance response (SCR, measured in siemens) during experiment runs, which is an indirect measure of sympathetic activity. Compare the blocks in which a pre-recorded visual threat (a video in which a hand is being pricked by a syringe needle) with baseline blocks and expect a higher SCR signal during visual threat blocks compared to the baseline. The SCR will be measured through a device connected to a dedicated laptop and electrodes that will be attached to the left index and middle fingers from participants. The SCR will be saved in log files and estimated a posteriori for each block using a general linear model and the weight regressors will be compared. There are no risks to the participants (since it is a passive measurement) the electrodes are compatible to the magnetic resonance environment.

Countries

Switzerland

Outcome results

None listed

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