Sense and Mind method: an innovative methodological approach to embodied rehabilitation
Annalisa Risoli1, Alessandro Antonietti1, Laura Colautti1
1Department of Psychology, Università Cattolica del Sacro Cuore, Milan, Italy.
The Sense and Mind (SaM) method uses embodied cognition to improve spatial cognition and executive functions in patients with neurodevelopmental and acquired neurocognitive impairments. This innovative approach leverages bodily experiences for neurorehabilitation.
Area of Science:
- Neuroscience
- Rehabilitation Medicine
- Cognitive Science
Background:
- Integrating neurorehabilitation research into clinical practice is essential.
- Embodied cognition offers a promising framework for neurorehabilitation.
- Existing methods may not fully address spatial cognition and executive functions through bodily experience.
Purpose of the Study:
- To propose and describe the novel Sense and Mind (SaM) method for neurorehabilitation.
- To target spatial cognition and executive functions using embodied cognition principles.
- To provide a theoretical and methodological framework for the SaM method.
Main Methods:
- The SaM method is grounded in neuroscientific evidence of embodied cognition, movement, spatial representation, mental imagery, and executive functions.
- It employs a restitutive approach with interventions at varying complexity levels, from voluntary movement programming to mental imagery.
- Goal-directed activities based on multimodal sensory experiences are utilized to enhance executive functions.
Main Results:
- The SaM method is designed to rehabilitate spatial cognition and executive functions.
- It facilitates interventions tailored to individual psychomotor profiles.
- The approach aims to improve daily life functioning by recovering crucial executive functions.
Conclusions:
- The Sense and Mind (SaM) method offers an innovative, embodied approach to neurorehabilitation.
- It holds potential for neuromotor and neuropsychological recovery across various disabilities.
- Further research with larger patient samples is needed to validate its efficacy.
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