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fMRI-guided individualized precise localization rTMS treatment for moderate to severe Alzheimer's disease

fMRI-guided individualized precise localization rTMS treatment for moderate to severe Alzheimer's disease

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2400086141
Enrollment
Unknown
Registered
2024-06-26
Start date
2024-07-01
Completion date
Unknown
Last updated
2024-07-08

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

Conditions

Alzheimer's disease

Interventions

precise localized group:precise localized rTMS
non-precise localized group:non-precise localized rTMS

Sponsors

Hangzhou Normal University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
55 Years to 80 Years

Inclusion criteria

Inclusion criteria: Health control group: (1) Age range from 55 to 80 years old; (2) The objective neuropsychological assessment score is within the normal range; (3) No concerns about cognitive decline or cognitive decline; (4) Through MRI safety screening; (5) Has not participated in any other clinical trials recently; (6) Sign the informed consent form for the participants. Cognitive impairment group: (1) Age range from 55 to 80 years old; (2) Clinical dementia rating (CDR) scores range from 2 to 3 points; (3) The score of the Mini Mental State Examination (MMSE) is less than 18 points; (4) Use a stable dose of therapeutic medication for at least 3 months prior to TMS treatment; (5) Through TMS safety screening, DBS electrodes without metal implantation, with no history of epilepsy or other neurological and psychiatric disorders, and no motor system diseases; (6) Through MRI safety screening, with no history of head injury or serious heart disease, and able to complete MRI scans; (7) Has not participated or is currently not involved in other TMS trials; (8) Sign the informed consent form for the participants.

Exclusion criteria

Exclusion criteria: Health control group: (1) Proactively withdraw from the experiment; (2) All fMRI images show head movement, translation>3mm, and rotation>3 °. Cognitive impairment group: (1) There are obvious adverse reactions; (2) Proactively withdraw from the experiment; (3) Those who are unable to determine the efficacy or whose data is incomplete, which affects the judgment of efficacy or safety; (4) All fMRI images show head movement, translation>3mm, and rotation>3 °.

Design outcomes

Primary

MeasureTime frame
clinical dementia rating;mini-mental state examination;

Secondary

MeasureTime frame
severe impairment battery, SIB;activity of daily living, ADL;Neuropsychiatric Inventory,NPI;CIBIC-Plus;

Countries

China

Contacts

Public ContactYufeng Zang

Hangzhou Normal university

zangyf@hznu.edu.cn+86 186 0651 7380

Outcome results

None listed

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