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Neuromotor function coupling effect study for sensorimotor assessment in stroke

Neuromotor function coupling effect study for sensorimotor assessment in stroke

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2400080636
Enrollment
Unknown
Registered
2024-02-04
Start date
2024-02-18
Completion date
Unknown
Last updated
2024-02-05

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

Conditions

stroke

Interventions

Healthy Control Group:None

Sponsors

Department of Rehabilitation Medicine, Shenzhen Second People's Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
30 Years to 70 Years

Inclusion criteria

Inclusion criteria: Stroke patients: ? Meet the diagnostic criteria for stroke; ? Vital signs are stable; ? Age 30-70 years old; ? Onset time = 1 month; ? Can complete cardiopulmonary exercise test; ? Cooperation S5Q = 3 points, can understand and actively participate in the assessment and training program; ?Patients or family members sign an informed consent form. Healthy subjects: ? aged 30-70 years; ? no previous history of stroke; ? complete basic information, voluntary participation in the study and signing of informed consent.

Exclusion criteria

Exclusion criteria: Stroke patients: ? vital signs are not stable, including respiratory rate =35 times/min; heart rate =145 times/min; systolic blood pressure =180mmHg or 110mmHg; body temperature =38.5? or =35?; ? moderate to severe aortic valve closure insufficiency; entrapment aneurysm; significant pulmonary arterial hypertension; valvular disease, congenital heart disease, Cardiomyopathy; severe left heart failure (NYHA class III-IV); uncontrolled arrhythmia: frequent premature beats, rapid atrial fibrillation, etc.; ?various bleeding disorders or bleeding tendency, or use of anticoagulants, INR>2.0; ? active phlebitis, venous thrombosis; Healthy subjects: ? subjects with previous psychiatric disorders; ? subjects with a history of serious cardiac disorders or surgeries; ? women during pregnancy or lactation; women who are concurrently enrolled in the program. Lactating women; ? Participated in other drug or medical device clinical trials during the same period;

Design outcomes

Primary

MeasureTime frame
Electroencephalography, peripheral motion signals during human movement;

Secondary

MeasureTime frame
Modified Rankin Scale,mRS;Longshi Assessment Scale of Activities of Daily Life, LSADL;Barthel index;

Countries

China

Contacts

Public ContactZha Fubing

Shenzhen Second People's Hospital

13923713995@139.com+86 139 2371 3995

Outcome results

None listed

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