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To develop the key technologies and systems for the assessment and early warning of elderly consciousness/cognitive impairment and multi-physical factor co-stimulation intervention——The study of the efficacy and mechanism of rTMS combined with tDCS in the treatment of elderly cognitive impairment

The study of the efficacy and mechanism of rTMS combined with tDCS in the treatment of elderly cognitive impairment.

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2400085208
Enrollment
Unknown
Registered
2024-06-03
Start date
2024-06-03
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

Mild Cognitive Impairment/Alzheimer's disease

Interventions

Sham group:Sham rTMS+Sham tDCS
rTMS group:rTMS+Sham tDCS
tDCS group:Sham rTMS+ tDCS
rTMS+tDCS group:rTMS+tDCS

Sponsors

The Third Affiliated Hospital, Sun Yat-sen University, Guangzhou, China
Lead Sponsor

Eligibility

Sex/Gender
All
Age
60 Years to No maximum

Inclusion criteria

Inclusion criteria: 1. Volunteers who are aged 60 years or older and sign the informed consent form. 2. Subjects or informants report progressive and evolving changes in memory function for =3 months. 3. Presence of mild cognitive impairment or mild to moderate dementia 4. Sufficient reading, writing, and audio-visual abilities to undergo neuropsychological testing. 5. If using cognitive-enhancing drugs (such as donepezil, memantine), must have been on a stable dose for at least 3 months with no dosage adjustments during the enrollment period.

Exclusion criteria

Exclusion criteria: 1. History of neurological diseases such as brain tumors, head trauma, stroke, epilepsy, Parkinson's disease, or mental disorders. 2. History of metabolic diseases including anemia, thyroid dysfunction, folate, vitamin B12 deficiency, and other conditions that can lead to cognitive decline. 3. History of alcohol abuse or drug use within the past 2 years before screening. 4. Post-craniotomy/cranial defect. 5. Presence of metal or electronic implants (e.g., pacemakers, cochlear implants, deep brain stimulators, aneurysm clips, internal fixation devices after ventriculoperitoneal shunt surgery, etc.). 6. Other serious illnesses that may affect the study. 7. Participation in other clinical studies concurrently.

Design outcomes

Primary

MeasureTime frame
Montreal Cognitive Assessment-Basic;Auditory Verbal Learning Test-Huashan;

Secondary

MeasureTime frame
Clinical Dementia Rating;Pittsburgh sleep quality index;Geriatric Depression Scale;Digit span test;Trail Making Test A and B;Digit Symbol Substitution Test;Verbal Fluency Test;Alzheimer's disease assessment scale-cognitive section;Clock Drawing Test;resting-state cerebral functional magnetic resonance imaging;Near infrared imaging spectrometer;electroencephalogram;

Countries

China

Contacts

Public ContactXiquan Hu

Department of Rehabilitation Medicine, The Third Affiliated Hospital, Sun Yat-sen University, Guangzhou, China

huxiquan@mail.sysu.edu.cn+86 189 2210 2910

Outcome results

None listed

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