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The study of central mechanism of electroacupuncture on EX-HN 1 improving sleep architecture and neurocognitive function using EEG-fMRI

The study of central mechanism of electroacupuncture on EX-HN 1 improving sleep architecture and neurocognitive function using EEG-fMRI

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR-INR-17013078
Enrollment
Unknown
Registered
2017-10-22
Start date
2018-01-01
Completion date
Unknown
Last updated
2017-11-06

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

Conditions

Insomnia after cerebral infarction with cognitive dysfunction

Interventions

Acupuncture group:Filiform needle acupuncture
Electroacupuncture group:Electroacupuncture
Electroacupuncture control group :Electroacupuncture
Sham acupuncture group:Filiform needle acupuncture
Drug control group :Estazolam Tablets
Blank group :None

Sponsors

The Second Affiliated Hospital of Heilongjiang University of Chinese Medicine
Lead Sponsor

Eligibility

Sex/Gender
All
Age
40 Years to 65 Years

Inclusion criteria

Inclusion criteria: (1) Meet the diagnostic criteria for insomnia after cerebral infarction with cognitive dysfunction; (2) Between 40-65 years old.The course of disease was 3 months ~2 years; (3) Lesions located in the basal ganglia of the non dominant hemisphere, stable condition, completing the assessment of scales independently; (4) Keeping seated, PSG overnight test and MRI scan can be accepted; (5) There were no sleep disorders, cognitive impairment, or transient sleep disturbances before the onset of the disease; (6) Recently (within 1 weeks), there was no treatment related to the trial; (7) Voluntarily participate and sign informed consent.;Inclusion criteria: (1) Meet the diagnostic criteria for insomnia after cerebral infarction with cognitive dysfunction; (2) Between 40-65 years old.The course of disease was 3 months ~2 years; (3) Lesions located in the basal ganglia of the non dominant hemisphere, stable condition, completing the assessment of scales independently; (4) Keeping seated, PSG overnight test and MRI scan can be accepted; (5) There were no sleep disorders, cognitive impairment, or transient sleep disturbances before the onset of the disease; (6) Recently (within 1 weeks), there was no treatment related to the trial; (7) Voluntarily participate and sign informed consent.;Inclusion criteria: (1) Meet the diagnostic criteria for insomnia after cerebral infarction with cognitive dysfunction; (2) Between 40-65 years old.The course of disease was 3 months ~2 years; (3) Lesions located in the basal ganglia of the non dominant hemisphere, stable condition, completing the assessment of scales independently; (4) Keeping seated, PSG overnight test and MRI scan can be accepted; (5) There were no sleep disorders, cognitive impairment, or transient sleep disturbances before the onset of the disease; (6) Recently (within 1 weeks), there was no treatment related to the trial; (7) Voluntarily participate and sign informed consent.;Inclusion criteria: (1) Meet the diagnostic criteria for insomnia after cerebral infarction with cognitive dysfunction; (2) Between 40-65 years old.The course of disease was 3 months ~2 years; (3) Lesions located in the basal ganglia of the non dominant hemisphere, stable condition, completing the assessment of scales independently; (4) Keeping seated, PSG overnight test and MRI scan can be accepted; (5) There were no sleep disorders, cognitive impairment, or transient sleep disturbances before the onset of the disease; (6) Recently (within 1 weeks), there was no treatment related to the trial; (7) Voluntarily participate and sign informed consent.;Inclusion criteria: (1) Meet the diagnostic criteria for insomnia after cerebral infarction with cognitive dysfunction; (2) Between 40-65 years old.The course of disease was 3 months ~2 years; (3) Lesions located in the basal ganglia of the non dominant hemisphere, stable condition, completing the assessment of scales independently; (4) Keeping seated, PSG overnight test and MRI scan can be accepted; (5) There were no sleep disorders, cognitive impairment, or transient sleep disturbances before the onset of the disease; (6) Recently (within 1 weeks), there was no treatment related to the trial; (7) Voluntarily participate and sign informed consent.

Exclusion criteria

Exclusion criteria: (1) Failure to meet diagnostic criteria; (2) Less than 40 years old, or more than 65 years old; (3) The course of disease was less than 3 months, or more than 2 years; (4) Patients with consciousness disorder or severe illness after cerebral infarction can not cooperate with related examinations; (5) Severe mental disorders or patients with previous history of mental illness; (6) Combined with severe cardiopulmonary failure or other serious somatic diseases; (7) Before the onset of cerebral infarction, the patient has been diagnosed with sleep disorders or cognitive impairment; (8) There are metal residues in the body, deep vein catheterization can not be scanned or affect the image quality; (9) Patients who took drugs for the central nervous system( diazepam, antidepressants, antipsychotics) in the last 1 months.;Exclusion criteria: (1) Failure to meet diagnostic criteria; (2) Less than 40 years old, or more than 65 years old; (3) The course of disease was less than 3 months, or more than 2 years; (4) Patients with consciousness disorder or severe illness after cerebral infarction can not cooperate with related examinations; (5) Severe mental disorders or patients with previous history of mental illness; (6) Combined with severe cardiopulmonary failure or other serious somatic diseases; (7) Before the onset of cerebral infarction, the patient has been diagnosed with sleep disorders or cognitive impairment; (8) There are metal residues in the body, deep vein catheterization can not be scanned or affect the image quality; (9) Patients who took drugs for the central nervous system( diazepam, antidepressants, antipsychotics) in the last 1 months.;Exclusion criteria: (1) Failure to meet diagnostic criteria; (2) Less than 40 years old, or more than 65 years old; (3) The course of disease was less than 3 months, or more than 2 years; (4) Patients with consciousness disorder or severe illness after cerebral infarction can not cooperate with related examinations; (5) Severe mental disorders or patients with previous history of mental illness; (6) Combined with severe cardiopulmonary failure or other serious somatic diseases; (7) Before the onset of cerebral infarction, the patient has been diagnosed with sleep disorders or cognitive impairment; (8) There are metal residues in the body, deep vein catheterization can not be scanned or affect the image quality; (9) Patients who took drugs for the central nervous system( diazepam, antidepressants, antipsychotics) in the last 1 months.;Exclusion criteria: (1) Failure to meet diagnostic criteria; (2) Less than 40 years old, or more than 65 years old; (3) The course of disease was less than 3 months, or more than 2 years; (4) Patients with consciousness disorder or severe illness after cerebral infarction can not cooperate with related examinations; (5) Severe mental disorders or patients with previous history of mental illness; (6) Combined with severe cardiopulmonary failure or other serious somatic diseases; (7) Before the onset of cerebral infarction, the patient has been diagnosed with sleep disorders or cognitive impairment; (8) There are metal residues in the body, deep vein catheterization can not be scanned or affect the image quality; (9) Patients who took drugs for the central nervous system( diazepam, antidepressants, antipsychotics) in the last 1 months.;Exclusion criteria: (1) Failure to meet diagnostic criteria; (2) Less than 40 years old, or more than 65 years old; (3) The course of disease was less than 3 months, or more than 2 years; (4) Patients with consciousness disorder or severe illness after cerebral infarction can not cooperate with related examinations; (5) Severe mental disorders or patients with previous history of mental illness; (6) Combined with severe cardiopulmonary failure or other serious somatic diseases; (7) Before the onset of cerebral infarction, the patient has been diagnosed with sleep disorders or cognitive impairment; (8) There are metal residues in the body, deep vein catheterization can not be scanned or affect the image quality; (9) Patients who took drugs for the central nervous system( diazepam, antidepressants, antipsychotics) in the last 1 months.

Design outcomes

Primary

MeasureTime frame
Polysomnography;Functional magnetic resonance imaging;Electroencephalogram;Psychomotor vigilance task;Karolinska Drowsiness Test;

Secondary

MeasureTime frame
Karolinska Sleepiness Scale;Short term memory experiment;Mini-Mental State Examination;Montreal Cognitive Assessment;Sleep diary;Actigraphy;Epworth Sleepiness Scale;

Countries

China

Contacts

Public ContactDongyan Wang;Dongyan Wang;Dongyan Wang;Dongyan Wang;Dongyan Wang ;;;;

Heilongjiang University Of Chinese Medicine;Heilongjiang University Of Chinese Medicine;Heilongjiang University Of Chinese Medicine;Heilongjiang University Of Chinese Medicine;Heilongjiang University Of Chinese Medicine

doctwdy@163.com;doctwdy@163.com;doctwdy@163.com;doctwdy@163.com;doctwdy@163.com+86 18646026767;+86 18646026767;+86 18646026767;+86 18646026767;+86 18646026767

Outcome results

None listed

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