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Study on the Regulatory Effect and Neural Mechanism of Temporal Interference Electrical Stimulation on the Thalamus of Healthy Adults

Study on the Regulatory Effect and Neural Mechanism of Temporal Interference Electrical Stimulation on the Thalamus of Healthy Adults

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2600117443
Enrollment
Unknown
Registered
2026-01-23
Start date
2026-01-23
Completion date
Unknown
Last updated
2026-01-27

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

Conditions

healthy human

Interventions

treatment 1:20Hz tTIS
control:sham tTIS
treatment2:80Hz tTIS

Sponsors

The Fourth Affiliated Hospital of Soochow University (Suzhou Dushu Lake Hospital)
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 45 Years

Inclusion criteria

Inclusion criteria: (1) Aged between 18 and 45 years, with no history of clearly diagnosed neurological, cardiovascular, or psychiatric diseases; (2) Being in a stable physical condition during the trial and at least one month prior to its initiation, without having taken any drugs that may significantly affect central nervous system excitability or cerebral blood flow; (3) Upper limb function: having normal function of both upper limbs, being right-handed, scoring Grade 5 in manual muscle testing, and free from sensory disturbances; (4) Consciousness and communication: being conscious, capable of normal communication, and without cognitive impairment; (5) Voluntarily participating in this trial and signing a written informed consent form.

Exclusion criteria

Exclusion criteria: (1) Subjects with intracranial implanted metal objects, pacemakers, or cochlear implants; (2) Subjects with deep sedation induced by general anesthetics (e.g., propofol) or centrally acting sedatives (e.g., benzodiazepines, opioids); (3) Subjects with frequent cardiac arrhythmias or frequent epileptic seizures; (4) Subjects with a history of mental illness, substance abuse, or alcoholism; (5) Subjects who have participated in other clinical trials involving brain stimulation or neuromodulation within the past 3 months.

Design outcomes

Primary

MeasureTime frame
Nine Hole Peg Test, 9HPT;

Secondary

MeasureTime frame
Grip Strength Test;choice reaction time task, CRTT;fMRI;EEG;fNIRS;tms;

Countries

china

Contacts

Public ContactMin Su

The Fourth Affiliated Hospital of Soochow University (Suzhou Dushu Lake Hospital)

sumin@suda.edu.cn+86 177 1266 1015

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026