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To study the efficacy and neural mechanism of repetitive transcranial magnetic stimulation combined with acupuncture in the treatment of subjective cognitive decline

To study the efficacy and neural mechanism of repetitive transcranial magnetic stimulation combined with acupuncture in the treatment of subjective cognitive decline

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500106455
Enrollment
Unknown
Registered
2025-07-24
Start date
2024-01-02
Completion date
Unknown
Last updated
2025-08-18

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

Conditions

Cognitive impairment patients

Interventions

Acupuncture group:The acupuncture treatment employed the "Tong Du Diao Shen" needling method, selecting acupoints Baihui, Shenting, Yintang, Sishencong, Anmian, Shenmen, Sanyinjiao, Hegu, and Taichong
Sham acupuncture group:Needling was performed only at the epidermal level, selecting acupoints Baihui, Shenting, Yintang, Sishencong, Anmian, Shenmen, Sanyinjiao, Hegu, and Taichong. The treatment cou
rTMS group:The rTMS treatment protocol is as follows: Stimulation Frequency: 10 Hz. Stimulation Site: Bilateral precuneus cortex. Stimulation Intensity: 100% of the resting motor threshold (RMT). Stim
Sham rTMS group:For the sham rTMS group, the treatment time, stimulated brain region, frequency, and preparation methods are identical to those of the patients receiving real

Sponsors

The Affiliated Brain Hospital of Nanjing Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
50 Years to 80 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria for healthy control group: (1) no complaints of memory disorders; (2) age - and education-matched normal cognitive performance; (3) Clinical Dementia Rating (CDR) = 0. Inclusion criteria for SCD group: Based on the criteria for SCD research published by SCD-I: (1) always complain about their memory problems; (2) subjective cognitive decline questionnaire (SCD-Q) >5; (3) age-and education-matched normal cognitive performance; (4) Activities of daily living were normal.

Exclusion criteria

Exclusion criteria: (1) less than 50 years old or more than 80 years old; (2) patients with contraindications to MRI scanning; (3) years of education: primary school or below; (4) dementia; (5) accompanied by a history of neuropsychiatric diseases, such as cerebrovascular disease, epilepsy, Parkinson's disease, multiple sclerosis, encephalitis, depression, schizophrenia, substance dependence, intracranial tumors and head trauma surgery, accompanied by diseases of the heart, liver, kidney, hematopoietic system and endocrine system that seriously affect cognitive function; (6) Visual and hearing impairment cannot meet the needs of cognitive assessment; (7) More infarcts and microbleeds were found in brain MRI.

Design outcomes

Primary

MeasureTime frame
Assessment of overall cognitive function;Multidimensional assessment of cognitive function;Subjective cognitive decline questionnaire(SCD-Q);Multimodal magnetic resonance imaging (MRI);

Countries

China

Contacts

Public ContactXingjian Lin

The Affiliated Brain Hospital of Nanjing Medical University

linxingjian@njmu.edu.cn+86 136 4519 1410

Outcome results

None listed

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