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Research on the mechanism of dual-target rTMS regulating the homeostasis of ECN-SN-DMN in chronic disorders of consciousness to promote consciousness recovery

Research on the mechanism of dual-target rTMS regulating the homeostasis of ECN-SN-DMN in chronic disorders of consciousness to promote consciousness recovery

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2600118755
Enrollment
Unknown
Registered
2026-02-10
Start date
2026-03-02
Completion date
Unknown
Last updated
2026-02-16

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

Conditions

prolonged disorders of consciousness

Interventions

Combined Left DLPFC-Cerebellar Stimulation Group:The sequential stimulation targeted the left DLPFC and the cerebellum, using an rTMS protocol at 10 Hz. Each stimulation train lasted 2 seconds, follow
Left DLPFC Stimulation Group:The left DLPFC alone was used as the stimulation target, with the cerebellum serving as the sham stimulation target. The rTMS parameters were as follows: stimulation inten

Sponsors

Jinhua Hospital of TCM Afliated to Zhejiang University of Traditional Chinese Medicine
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 75 Years

Inclusion criteria

Inclusion criteria: 1.Meet the diagnostic criteria for pDoC as outlined in the Chinese Expert Consensus on the Diagnosis and Treatment of Disorders of Consciousness. 2.Age between 18 and 75 years; 3.Normal cognitive, interpersonal, visual, and auditory functions prior to brain injury; 4.Stable vital signs; 5.Willingness of family members or authorized representatives to participate in the study, with signed informed consent.

Exclusion criteria

Exclusion criteria: 1.Presence of severe complications in systems such as respiratory or circulatory systems, with unstable vital signs; 2.Patients with concomitant status epilepticus; 3.Presence of intracranial infection; 4.Age greater than 75 years or less than 18 years; 5.CT or MRI showing significant cerebral edema; 6.Unwillingness or inability of family members or guardians to cooperate with the treatment, or refusal to sign the informed consent form; 7.Presence of metal foreign bodies in the body, cardiac pacemakers, arterial clips, significant skull defects, unresolved hematomas, or other factors affecting TMS-EEG signal acquisition; 8.Unstable clinical condition or presence of other severe cardiac, pulmonary, hepatic, or renal diseases; 9.Currently receiving other clinical central nervous system intervention therapies.

Design outcomes

Primary

MeasureTime frame
Coma Recovery Scale-Revised;

Secondary

MeasureTime frame
Nociception Coma Scale-Revised;Disability Rating Scale;

Countries

China

Contacts

Public ContactLingyan Wang

Jinhua Hospital of TCM Afliated to Zhejiang University of Traditional Chinese Medicine

lynna0312@126.com+86 182 5709 2270

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 19, 2026