Electrotactile Frequency, Amplitude, and Temporal Gap Discrimination in Young Adults, Older Adult… (NCT07656675) | Clinical Trial Compass
Not Yet RecruitingNot Applicable
Electrotactile Frequency, Amplitude, and Temporal Gap Discrimination in Young Adults, Older Adults, and Stroke Survivors
80 participantsStarted 2026-06-11
Plain-language summary
The purpose of this study is to evaluate and compare sensory discrimination ability for electrotactile stimulation among young adults, older adults, and patients with stroke. Participants will receive non-invasive electrotactile stimulation through electrodes attached to the skin of the upper limb, such as the fingertip, palm, elbow, or shoulder, depending on the stimulation condition. The study will assess discrimination thresholds for changes in stimulation frequency, stimulation amplitude, and temporal gaps in stimulation, together with task accuracy and reaction time. The results are expected to provide foundational data for sensory assessment, electrotactile feedback design, and sensory-based rehabilitation technologies for older adults and stroke patients.
Who can participate
Age range
19 Years – 70 Years
Sex
ALL
See this in plain English?
AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.
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…
Questions worth asking your doctor
Bring these to your next appointment. They're a starting point for a shared conversation — not a sign you qualify or a recommendation to enrol.
1This trial is studying how well people can detect differences in electrical touch sensations on the skin — since it's comparing stroke survivors to healthy adults, could this type of sensory testing tell us anything useful about my own stroke-related sensation changes?
2The trial isn't recruiting yet, so if my doctor thinks this could be relevant for me, how would we find out when enrollment actually opens and whether I might be a candidate at that point?
3This study seems to be measuring basic sensory perception rather than offering a treatment — does that mean there's no direct therapeutic benefit for me as a participant, and if so, what would my involvement actually look like day to day?
4Since this involves applying small electrical pulses to the skin to test sensation, what should I know about any discomfort or risks that might be associated with electrotactile stimulation, especially given my stroke history?
5Are there standard clinical assessments for post-stroke sensory loss that my care team could do now, and how does what this research trial is measuring compare to those existing tools?
Generated to help you prepare — always confirm anything about your own eligibility and care with the study team and your doctor.
Questions for the trial coordinator
The trial coordinator is the person who runs the study day to day. These cover the practical side — logistics, costs, and what taking part would actually mean for your life. The study team confirms whether you meet the criteria; these are questions to ask, not a sign you qualify.
1What does taking part actually involve week to week — how many visits, where, and how long does each one take?
2What costs are covered by the study, and what might I have to pay for myself, including travel, parking, or time off work?
3What happens during screening, and what happens if the study team confirms I don't meet the criteria after those tests?
4Who pays for the scans, blood work, and other tests the trial requires — the study, my insurance, or me?
5How will being in the trial affect my regular care, and will my own doctor stay informed and involved?
6Can I leave the trial at any point if I change my mind, and what would happen to my care if I do?
A starting point for the conversation — always confirm anything about your own eligibility, costs, and care with the study team and your doctor.
What they're measuring
1
Just Noticeable Difference for Electrotactile Sensory Discrimination
Timeframe: During the experimental session, up to 2 days for young and older adult participants and 1 day for stroke patients