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Effect of sensorimotor observation based on mirror visual feedback on hand and upper limb rehabilitation after stroke

Effect of sensorimotor observation based on mirror visual feedback on hand and upper limb rehabilitation after stroke

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2300076838
Enrollment
Unknown
Registered
2023-10-20
Start date
2023-10-20
Completion date
Unknown
Last updated
2023-10-22

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

Conditions

Stroke

Interventions

Mirror observation group:Sensorimotor observation therapy based on mirror vision feedback
control group:Pseudo-sensorimotor observation (static landscape observation)

Sponsors

Huashan Hospital, Fudan University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: ? Age 18-80 years old, right-handed, with normal or corrected vision; ? Confirmed by head computed tomography (CT) or magnetic resonance imaging (MRI) as first-time, unilateral cerebral hemorrhage/infarction; ? The diagnosis meets the criteria of "2019 Key Diagnostic Points for Various Major Cerebrovascular Diseases in China" formulated by the Cerebrovascular Disease Group of the Neurology Branch of the Chinese Medical Association; ? The onset time is 1 week to 6 months, and the condition is stable; ? No serious cognitive impairment, MoCA score = 22 points, can cooperate with assessment and treatment; ? The Brunnstrom staging of the upper limb and hand on the hemiplegic side ranges from stage I to stage IV, with moderate to severe hemiplegia, and the main flexors of the wrist and elbow are not accompanied by severe spasms, including wrist flexors and biceps brachii muscle tension = level 2 (modified Ashworth scale); ? Have not received mirror therapy; ? Can be held in a sitting position for at least 60 minutes; ? Voluntarily participate in this study and have an informed consent form signed by oneself or on behalf of his immediate family.

Exclusion criteria

Exclusion criteria: ? The condition deteriorates, and a new infarction stove or a large area of cerebral infarction; ? The history of epilepsy, cerebral hemorrhage and severe heart, lung, liver, kidney and other important organ failure, uncontrollable hypertension, arrhythmia, severe severe, serious coronary heart disease, diabetes complications are not good; ? Those who are allergic to test -related equipment and components such as conductive cream, frosted cream, frosted plants;?There are metal implants or skull defects, pregnancy, breastfeeding, or no reliable contraceptive measures for childbearing age; ? Receive central intervention and regulation technologies such as motion observation and motion imagination during the test;Those who have poor compliance.

Design outcomes

Primary

MeasureTime frame
Fugl-Meyer Assessment for upper extremity motor function;

Secondary

MeasureTime frame
Action ResearchArm Test;Box and Block Test;Hand grip strength test;Modified Barthel Index;Pinch force test;Brunnstrom stage;Modified Ashworth scale;Fugl-Meyer Assessment for upper extremity sensory function;Two-point discrimination test;Semmes-Weinstein Monofilament test;Treatment compliance (completion frequency and completion rate);electroencephalogram (EEG);Magnetic resonance imaging(MRI);

Countries

China

Contacts

Public ContactJie Jia

Huashan Hospital, Fudan University

shannonjj@126.com+86 136 1172 2357

Outcome results

None listed

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