Skip to content

A whole-process medical record management model based on family and community for graded diagnosis and rehabilitation of neurocognitive disorders (Magnetoelectric stimulation intervention)

A whole-process medical record management model based on family and community for graded diagnosis and rehabilitation of neurocognitive disorders (Magnetoelectric stimulation intervention)

Status
Recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2000039141
Enrollment
Unknown
Registered
2020-10-19
Start date
2020-10-15
Completion date
Unknown
Last updated
2021-01-18

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

Conditions

Neurocognitive disorders

Interventions

Magnetoelectric stimulation group:Magnetoelectric stimulation for 30 minutes at 20Hz in the right dorsolateral prefrontal lobe
Control group:False stimulus with the same stimulus time and parameters

Sponsors

Shanghai Jiaotong University
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1. Community elderly or outpatients; 2. The patients (suspected dementia, mild dementia and moderate dementia) who met the above diagnostic criteria for cognitive impairment included: CDR score 0.5-2; MMSE <= 26 points; MMSE <= 26 points; 3. The age of patients over 60 years old is not limited to men and women; 4. Patients with primary school or more than 5 years of education; 5. Informed consent signed by the patient or his legal guardian.

Exclusion criteria

Exclusion criteria: 1. Patients with serious physical diseases and suicide attempts were excluded; 2. Patients with history of stroke, cerebrovascular accident, epilepsy and craniocerebral trauma in recent one month; 3. Those patients who excluded other Axis I mental disorders, including schizophrenia, affective disorder and anxiety spectrum disorder, were interviewed by SCID; 4. The patients with poor audiovisual function or physical diseases who could not complete the cognitive and emotional assessment were excluded; 5. The researcher thinks that there are other situations that are not suitable for participating in the clinical trial.

Design outcomes

Primary

MeasureTime frame
The Cognitive Assessment;The Cognitive Assessment;

Countries

China

Contacts

Public ContactLi Xia

Shanghai Mental Health Center

ja_1023@aliyun.com+86 13774272543

Outcome results

None listed

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