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Transcranial Temporal Interference Stimulation for Cognitive Impairment in Chronic Cerebral Hypoperfusion: A Feasibility and Mechanistic Study

Transcranial Temporal Interference Stimulation for Cognitive Impairment in Chronic Cerebral Hypoperfusion: A Feasibility and Mechanistic Study

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2600117802
Enrollment
Unknown
Registered
2026-01-29
Start date
2026-02-10
Completion date
Unknown
Last updated
2026-02-02

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

Conditions

Chronic cerebral hypoperfusion (CCH)

Interventions

Gamma-tTIS intervention group (self-control):Hippocampus-targeted 40-Hz Gamma-tTIS: dual-channel carriers at 2000/2040 Hz generating a 40-Hz envelope
total injected current 2.0 mA
20 min/session
once daily, 5 days/week for 4 weeks (20 sessions).

Sponsors

Beijing Rehabilitation Hospital, Capital Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
40 Years to 80 Years

Inclusion criteria

Inclusion criteria: 1 Age 40–80 years. 2 Imaging evidence of chronic cerebral hypoperfusion (e.g., brain MRI showing white matter hyperintensities, or TCD/CTA indicating cerebral atherosclerosis/stenosis without acute infarction). 3 Subjective complaint of memory decline, with a Montreal Cognitive Assessment (MoCA) score < 26. 4 Clinical Dementia Rating (CDR) = 0.5 (mild). 5 Pharmacological treatment (including cholinesterase inhibitors and/or memantine) has remained stable for at least 3 months prior to enrollment, and the participant agrees not to change the medication regimen throughout the study period.

Exclusion criteria

Exclusion criteria: 1 History of neurodegenerative diseases (e.g., Alzheimer’s disease, Parkinson’s disease, dementia with Lewy bodies), new-onset acute stroke within the past 3 months, brain tumor, traumatic brain injury, or any other neurological disorder that may affect cognition. 2 Severe or unstable systemic diseases (e.g., heart failure, uncontrolled diabetes mellitus, severe infection). 3 Diagnosed major depressive disorder, bipolar disorder, schizophrenia, or other psychiatric disorders that may affect cognition. 4 Presence of metallic implants in the body (e.g., cardiac pacemaker, intracranial metallic implants). 5 History of seizures or uncontrolled epilepsy. 6 Severe skull defect. 7 Severe claustrophobia with inability to tolerate or complete MRI (fMRI) examination.

Design outcomes

Primary

MeasureTime frame
Auditory Verbal Learning Test (AVLT) total score / delayed recall score;Montreal Cognitive Assessment (MoCA) total score;

Secondary

MeasureTime frame
Trail Making Test (TMT) B–A (time difference);Resting-state EEG band power;Resting-state fMRI hippocampus-to-whole-brain functional connectivity (FC);

Countries

China

Contacts

Public ContactShuyan Qie; Chenye Qiao

Beijing Rehabilitation Hospital, Capital Medical University

shuyanpb@163.com+86 138 1051 0280

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 7, 2026