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Research on the application and Mechanism of Transcranial Temporal Interference Stimulation Combined with Median Nerve Stimulation in patients with prolonged disorders of consciousness based on multi-modal assessment

Research on the application and Mechanism of Transcranial Temporal Interference Stimulation Combined with Median Nerve Stimulation in patients with prolonged disorders of consciousness based on multi-modal assessment

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2600119228
Enrollment
Unknown
Registered
2026-02-24
Start date
2026-03-01
Completion date
Unknown
Last updated
2026-03-02

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

Conditions

Patients with disorders of consciousness 28 days to 1 year after brain injury

Interventions

real TI+real MNS group:Transcranial Temporal Interference Stimulation combined with Median Nerve Stimulation
sham TI+real MNS group:Transcranial Temporal Interference Stimulation

Sponsors

Xuzhou Rehabilitation Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 70 Years

Inclusion criteria

Inclusion criteria: 1. Patients aged 18-80 years, diagnosed with Coma, Vegetative State (VS), or Minimally Conscious State (MCS) according to the Coma Recovery Scale-Revised (CRS-R) based on multiple CRS-R assessments, with a disease duration of =28 days and =12 months; 2. Etiology includes traumatic brain injury, cerebrovascular accident, or hypoxic-ischemic encephalopathy; 3. Stable clinical condition: vital signs stable without the need for high-dose sedative or analgesic agents; 4. No history of alcohol abuse, substance abuse, or psychiatric disorders; 5. No administration of sedatives or muscle relaxants within 24 hours prior to behavioral assessments and MRI examinations; 6. Absence of severe comorbidities: no significant structural damage to bilateral brain stem, thalamus, or spinal cord;no severe cardiac, pulmonary, hepatic, or renal failure;cord;no severe cardiac, pulmonary, hepatic, or renal failure; 7. Informed consent obtained: written informed consent provided by legal guardians.

Exclusion criteria

Exclusion criteria: 1. Unstable vital signs; 2. Intracranial retention of metallic objects; 3. History of epilepsy or psychiatric disorders; 4.Presence of severe functional impairment in critical organs such as the heart, liver, or kidneys; 5. Administration of sedatives or neuromuscular blocking agents within 24 hours prior to behavioral assessments or MRI examinations.

Design outcomes

Primary

MeasureTime frame
coma recovery scale-revised;

Secondary

MeasureTime frame
Electroencephalograph;near-infrareed spectroscopy;functional Magnetic Resonance Imaging;

Countries

China

Contacts

Public ContactJiaojiao Chen

Xuzhou Rehabilitation Hospital

yeyeyi0329@163.com+86 516 8732 6393

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Mar 14, 2026