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Research on the Rehabilitation Efficacy and Neural Mechanisms of SMART Technology in Improving Hand Function in Stroke Patients with Hemiplegia

Study on the Therapeutic Efficacy and Neural Mechanisms of Sensory Movement Reconstruction Technology (SMART) in Hand Function Rehabilitation for Post-Stroke Hemiplegic Patients

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2600126512
Enrollment
Unknown
Registered
2026-06-10
Start date
2026-07-01
Completion date
Unknown
Last updated
2026-06-15

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

Conditions

Hemiplegia and upper limb hand dysfunction following ischemic/hemorrhagic stroke

Interventions

Routine Rehabilitation Control Group:Conventional Upper Limb Rehabilitation Intervention
SMART Intervention Experimental Group:SMART structured upper limb rehabilitation intervention

Sponsors

Lanzhou City Traditional Chinese Medicine Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 75 Years

Inclusion criteria

Inclusion criteria: 1.Meets the diagnostic criteria outlined in the "China Guidelines for Diagnosis and Treatment of Acute Ischemic Stroke 2023" and the "China Guidelines for Diagnosis and Treatment of Intracerebral Hemorrhage 2023", with a definitive diagnosis confirmed by cranial CT/MRI imaging studies. 2.The disease course lasts 3 to 12 months, during which the patient is in the recovery phase of stroke. 3.Age range: 18–75 years; gender unrestricted; 4.The Fugl-Meyer Motor Function Score (FMA-UE) for the affected upper limb ranges from 22 to 58 points, indicating significant hand dysfunction. 5.The Mini-Mental State Examination (MMSE) score is =17; the patient exhibits clear consciousness and no significant cognitive impairment, and can cooperate fully with rehabilitation training and assessment. 6.Life signs are stable, with no severe complications. 7.The patient and their family members have provided full informed consent, voluntarily participated in this study, and signed the written informed consent form.

Exclusion criteria

Exclusion criteria: 1.Severe cognitive impairment, sensory aphasia, mixed aphasia; inability to understand instructions or cooperate with training and assessment procedures. 2.The patient has severe combined dysfunction of vital organs such as the heart, liver, kidneys, and respiratory system, making rehabilitation interventions intolerable. 3.The modified Ashworth Spasm Scale (MAS) for the affected upper limb shows a spasm grade>3, with severe spasms significantly impairing athletic performance. 4.Orthopedic or neurological conditions such as fractures, dislocations, rheumatoid arthritis, or peripheral nerve injuries in the affected upper limb that interfere with hand function assessment and training. 5.Patients with a history of traumatic brain injury, Parkinson's disease, motor neuron diseases, or other central nervous system disorders; 6.Individuals who have undergone interventions affecting upper limb function, such as botulinum toxin injections or surgical procedures, within the past 3 months; 7.Women during pregnancy or lactation, individuals with mental disorders, and those with alcoholism or drug dependence;

Design outcomes

Primary

MeasureTime frame
Fugl-Meyer Upper Extremity Function Assessment (FMA-UE);Wolf Motor Function (WMFT);Modified Barthel Index (MBI);Lindmark Functional Assessment Score;

Secondary

MeasureTime frame
Motor Evoked Potential (MEP);Quantitative Sensory Testing of the Upper Limb;

Countries

China

Contacts

Public Contacttao Xu

Lanzhou City Traditional Chinese Medicine Hospital

93649300@qq.com+86 931 294 2437

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Jun 21, 2026