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The multimodal method analysis study on the integrated regulation of Yanglingquan needling on hemiplegic patients's brain network

The multimodal method analysis study on the integrated regulation of Yanglingquan needling on hemiplegic patients's brain network

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2200061609
Enrollment
Unknown
Registered
2022-06-29
Start date
2015-01-01
Completion date
Unknown
Last updated
2023-04-03

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

Conditions

hemiplegia after cerebral infarction

Interventions

Test group:Acupuncture at Yanglingquan
Healthy control group:Acupuncture at Yanglingquan

Sponsors

Dongzhimen Hospital, Beijing University of Chinese Medicine
Lead Sponsor

Eligibility

Sex/Gender
All
Age
40 Years to 75 Years

Inclusion criteria

Inclusion criteria: Hemiplegia patients test group: 1. Patients with cerebral infarction whose course of disease is 1.5 months conform to the diagnostic criteria of cerebral infarction (Chinese Guidelines for the Diagnosis and Treatment of Acute Ischemic Stroke 2014); 2. Right-handed; 3. Aged 40 - 75 years, both men and women are eligible; 4. In patients with left hemiplegia, the infarct was located in the right basal ganglia and/or the radiation coronal region; 5. The patient has unconscious disorder and the condition is relatively stable; 6. No psychotropic drugs have been taken in the past month; 7. Here is no metal in the body and no contraindication of nuclear magnetic resonance examination; 8. The patient himself or his immediate family members sign the informed consent. Healthy subjects group: 1. Right-handed; 2. Aged 40 - 75 years, both men and women are eligible; 3. Those who have been proved to be in the range of physical health by physical examination have no organic or significant functional diseases; 4. No family genetic history of mental and nervous system; 5. No research similar to this experiment has been conducted; 6. There were no physical abnormalities (such as cold, headache, cough, etc.) during the experimental period; 7. No excitatory drugs have been taken in the past two months; 8. There are no metal implants in vivo and no contraindications for functional magnetic resonance imaging. 9. Subjects signed the informed consent and volunteered to participate in the experiment.

Exclusion criteria

Exclusion criteria: Hemiplegia patients test group: 1. Combining with psychiatric disorders or any other serious primary diseases; 2. Being pregnant, lactating or menstrual; 3. Severe skull anatomical asymmetry or definite lesions being found by MRI scans; 4. Taking part in similar neuroimaging test within 1 month. Healthy subjects group: 1. Being menstrual, pregnant or lactating; 2. Severe skull anatomical asymmetry or definite lesions being found by MRI scans.

Design outcomes

Primary

MeasureTime frame
Granger analysis;

Secondary

MeasureTime frame
Fugl-Meyer Assessment;National Institutes of Health Stroke Scale;Needle Sensation Assessment Scale;Fractional anisotropy (FA);Modified Ashworth scale;Hamilton Depression Scale (HAMD);Brunnstrom Scale;Mini-Mental State Examination (MMSE);Motricity Index;Barthel Index;

Countries

China

Contacts

Public ContactYihuai Zou

Dongzhimen Hospital, Beijing University of Chinese Medicine

zouyihuai2004@163.com+86 10 84013130

Outcome results

None listed

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