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Electric touch test could pave way for smarter stroke rehab

NCT ID NCT07656675

Knowledge-focused Sponsor: Sungkyunkwan University Source: ClinicalTrials.gov ↗

What the study statuses mean

This study's is highlighted.

Recruitment status, easiest to join first

Recruiting now
This trial is taking on new participants right now.
Not yet recruiting This study
Registered, but not yet taking participants.
By invitation only
Not open to general applications. Only people the study team invites can take part.
Paused
Paused for now. It may or may not start again.
Ongoing
Running, but no longer taking on new participants.
Completed
The trial has finished. Results may not be published yet.
Stopped early
Stopped early, before it reached the end. That can be for many reasons, including safety.
Cancelled
Cancelled before anyone took part.

Expanded access (not trials)

Expanded access
Not a trial. This treatment can be requested outside a study, case by case, for people who qualify.
Expanded access (paused)
Not a trial. The treatment can normally be requested outside a study, but is unavailable right now.
Expanded access (ended)
Not a trial. The treatment could once be requested outside a study, but no longer can.
Approved
The treatment has been approved, so it is available normally rather than through this programme.

When the status isn't known

Details not published
The full record has not been published yet, so there is little to show here.
Status unknown
This status has not been confirmed recently, so it may be out of date.

First seen Jun 26, 2026 · Last updated Jun 27, 2026 · Updated 1 time

Summary

This study will compare how young adults, older adults, and stroke survivors sense small electrical pulses on their skin. Researchers will measure the smallest changes in pulse frequency, strength, and timing that people can detect. The goal is to gather basic information to improve feedback systems used in rehabilitation after a stroke.

What this could mean

Our plain-language read of the trial. This is informational only, not medical advice or a prediction.

What this could lead to
If successful, this could help design better sensory feedback systems for stroke rehabilitation and assistive technologies.
What could go wrong
This is an early-stage observational study with only 80 participants, so results may not apply broadly. It does not test a treatment or therapy.

This is an AI summary of the original study and may miss details. Read our disclaimer.

Study facts

What this study's own registry entry says, in plain language.

Phase

Not a phased trial

Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.

Participants

About 80 people

The number the study aims to enrol. It can still change while the study runs.

Expected to start

Jun 2026

An estimate. Start dates often move.

Expected to finish

Apr 2028

An estimate. End dates often move.

Lead sponsor

Other sponsor

The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.

Who can take part

This study's own entry requirements. Only the study team can say for certain whether you qualify.

Ages

19 to 70 years

Sex

Anyone

Healthy volunteers

Accepted

You do not need to have the condition being studied to take part.

Show the full entry requirements

Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.

Inclusion Criteria: * Young Adult Group: * Age 19 to 54 years. * Has tactile sensation in the hands and fingers. * Provides voluntary written informed consent personally or through a legally authorized representative, if applicable. Older Adult Group: * Age 55 to 70 years. * Has tactile sensation in the hands and fingers. * Provides voluntary written informed consent personally or through a legally authorized representative, if applicable. Stroke Patient Group: * Age 19 years or older. * Diagnosis of ischemic or hemorrhagic stroke. * Stroke confirmed by CT or MRI. * Stroke accompanied by proprioceptive sensory impairment. * Residual tactile sensation in the fingertip. * Provides voluntary written informed consent personally or through a legally authorized representative, Exclusion Criteria: * Young and Older Adult Groups: * Absence of tactile sensation in the hands or fingers. * Congenital deformity of the hands or fingers. * Presence of a major pre-existing neurogenic disease. * Presence of a major psychiatric disorder, such as major depressive disorder, schizophrenia, bipolar disorder, or dementia. * Implanted pacemaker. Stroke Patient Group: * Difficulty communicating due to K-MMSE score \< 23, severe language impairment, or similar condition. * Absence of tactile sensation in the hands or fingers. * Congenital deformity of the hands or fingers. * Severe pain during elbow joint or finger movement. * Progressive or unstable stroke. * Presence of hemispatial neglect. * Presence of a major pre-existing neurogenic disease. * Presence of a major psychiatric disorder, such as major depressive disorder, schizophrenia, bipolar disorder, or dementia. * Implanted pacemaker.

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Conditions

The condition(s) this trial relates to.

stroke disorder

As listed by the trial registrant

The condition terms exactly as the trial's registrant entered them.

Stroke

How to take part

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  1. The official record

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    Open the record ↗

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More trials for these conditions

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