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Enhanced Human Sensorimotor Integration Via Self-modulation of the Somatosensory Activity

Enhanced Human Sensorimotor Integration Via Self-modulation of the Somatosensory Activity

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06814873
Enrollment
39
Registered
2025-02-07
Start date
2023-05-10
Completion date
2024-03-31
Last updated
2025-02-07

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

Conditions

Somatosensory Evoked Potentials, and Electroencephalography

Brief summary

The purpose of this study is to examine the functional and structural modification effects on the brain of a non-invasive experimental device applied to the head and forearms of healthy subjects during motor recall training. The experimental device used in this study is the Brain-Machine Interface (hereinafter referred to as BMI), which is under development in the principal investigator's laboratory. The BMI consists of an arithmetic unit that processes the results in real time using a personal computer, a depth ray that displays the results, a transcutaneous electrical stimulator that is driven based on the results of the arithmetic, and an exoskeletal motor assist device that is driven based on the results of the arithmetic.

Detailed description

This study does not fall under the category of 'medical research involving human subjects' or 'clinical research subject to legal regulations' in Japan, and the appointment of a principal investigator (PI) is not required. For the convenience of registry submission, the name of the principal investigator field has been filled with the name of the study representative (a non-physician).

Interventions

BEHAVIORALNeurofeedback

The participants received visual feedback of the processed result of neural signals acquired online.

BEHAVIORALSham-feedback

Previously recorded neural signals are processed and presented to participants as if the signals from them are processed online.

Sponsors

Keio University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
BASIC_SCIENCE
Masking
SINGLE (Subject)

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
Yes

Exclusion criteria

* History of neurological disorder

Design outcomes

Primary

MeasureTime frameDescription
Somatosensory evoked potentialFrom the timing of pre-training evaluation (before the intervention) to the end of evaluation (after the intervention), with the intervention lasting 30 minutes.Median nerve stimulation elicits the somatosensory evoked potentials. Their amplitude was calculated.

Secondary

MeasureTime frameDescription
Touch typing performanceFrom the timing of pre-training evaluation (before the intervention) to the end of evaluation (after the intervention), with the intervention lasting 30 minutes.A touch typing task was employed to test sensorimotor integration performance

Countries

Japan

Outcome results

None listed

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