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The effect of intelligent upper limb rehabilitation training mode based on the 'central peripheral coupling effect' on upper limb and hand function in middle-aged and young stroke patients

The effect of intelligent upper limb rehabilitation training mode based on the 'central peripheral coupling effect' on upper limb and hand function in middle-aged and young stroke patients

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500097887
Enrollment
Unknown
Registered
2025-02-26
Start date
2023-10-07
Completion date
Unknown
Last updated
2025-03-03

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

Conditions

Stroke

Interventions

Control group:Conventional rehabilitation therapy for stroke combined with traditional upper limb occupational therapy, once a day, five times a week, with a treatment course of four weeks.
Intelligent rehabilitation Group:Conventional rehabilitation therapy for stroke combined with an upper limb rehabilitation training system and pneumatic mirror rehabilitation gloves, once a day, five

Sponsors

Chengdu Pidu District People's Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 59 Years

Inclusion criteria

Inclusion criteria: 1.The clinical diagnosis of enrolled patients with cerebral infarction conforms to the diagnostic criteria of the '2018 Chinese Guidelines for the Diagnosis and Treatment of Acute Ischemic Stroke'; Patients with cerebral hemorrhage included in the study were clinically diagnosed in accordance with the diagnostic criteria outlined in the Chinese Guidelines for the Diagnosis and Treatment of Cerebral Hemorrhage; 2. The results of imaging examinations such as head CT or MRI should support the clinical diagnosis of stroke. 3.Age range: 18-59 years old; 4.First onset, course of illness = 23, able to understand instructions and execute them; 9.The patient or family member signs an informed consent form.

Exclusion criteria

Exclusion criteria: 1.Severe deformity or loss of fingers affects functions such as finger to finger and lateral pinching; 2.Severe visual impairment; 3.Severe cognitive impairment; 4.Skin infections, injuries, or damages that affect functional exercise in the affected upper limb or hand; 5.Severely limited mobility of the shoulder, elbow, wrist, finger joints, etc. existed before the onset of the disease; 6.Severe cardiac dysfunction; 7.Serious mental disorders; 8.Abuse of alcohol, drugs, or other substances that affect central nervous system function; 9.Due to other reasons, the patient cannot cooperate in completing rehabilitation assessment and treatment; 10.Not in a working state before illness.

Design outcomes

Primary

MeasureTime frame
Fugl-Meyer assess-ment-upper extremities score;Canadian occupational performance measure score;Action research arm test score;Modified Ashworth scale score;the National Institutes of Health Str oke Scale Score;modified barthel index;

Secondary

MeasureTime frame
Self-rating anxiety scale score;Self-rating depression scale score;Quantitative EEG Changes;Diffusion Tensor Imaging Changes;Serum BDNF;Serum miRNA-132;

Countries

China

Contacts

Public ContactLimei Wang

Chengdu Pidu District People's Hospital

wang_li_mei_2006@126.com+86 135 5884 1815

Outcome results

None listed

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