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the effects of hand and brain sensory rehabilitation on upper limb function and daily life activity after stroke:a randomized controlled trial

the effects of hand and brain sensory rehabilitation on upper limb function and daily life activity after stroke:a randomized controlled trial

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR1900027914
Enrollment
Unknown
Registered
2019-12-04
Start date
2020-01-01
Completion date
Unknown
Last updated
2020-03-16

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

Conditions

Neurological rehabilitation

Interventions

Group 2:Hand and brain perception training
Group 1:occupational therapy

Sponsors

Huashan Hospital affiliated to Fudan University, Jing'An District Central Hospital affiliated to Fudan University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: 1. the first unilateral stroke (cerebral infarction and cerebral hemorrhage); 2. cerebral infarction patients: meet the diagnostic criteria of Chinese guidelines for diagnosis and treatment of acute ischemic stroke 2014; 3. patients with cerebral hemorrhage: meet the diagnostic criteria of Chinese guidelines for diagnosis and treatment of cerebral hemorrhage 2014; 4. cerebral infarction or cerebral hemorrhage confirmed by CT or MRI; 5. stroke patients aged 18 to 80 years; 6. onset time: 4 weeks to 3 years; 7. the patient's vital signs were stable, with few or no serious complications; 8. modified RANKIN scale (MRS) score 1-4; 9. national institutes of health stroke scale (NIHSS) score 1-20; 10. signed informed consent and completed the test according to the plan.

Exclusion criteria

Exclusion criteria: 1. patients with previous severe heart, lung, liver, kidney and other important organ failure, uncontrolled hypertension, arrhythmia, severe coronary heart disease and diabetes complications are poorly controlled; 2. the disease deteriorates, new infarcts or large-scale cerebral infarction appear, or the patients with other serious diseases of the system are not qualified for the study; 3. severe speech, attention, hearing, visual, intellectual, mental or cognitive impairment; Previous history of cognitive impairment, neuropsychiatric history, drug and alcohol abuse; Severe cramps or pain; 4. failure to cooperate with functional evaluation and poor compliance; 5. recently participated in other clinical trials.

Design outcomes

Primary

MeasureTime frame
Sensory function scale;

Countries

China

Contacts

Public ContactJie Jia

HuaShan Hospital affiliated to Fudan University

1174060571@qq.com+86 13611722357

Outcome results

None listed

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