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Study on the difference of sEMG delivery in key muscles of stroke patients after the intervention of virtual reality and upper limb robotic training

Study on the difference of sEMG delivery in key muscles of stroke patients after the intervention of virtual reality and upper limb robotic training

Status
Active, not recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2200063546
Enrollment
Unknown
Registered
2022-09-10
Start date
2022-10-01
Completion date
Unknown
Last updated
2023-04-17

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

Conditions

Stroke

Interventions

experimental group one:conventional therapy, upper limb robot training
experimental group two:conventional therapy, upper limb robot training, VR
control group:conventional therapy

Sponsors

Shanghai Seventh People's Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
35 Years to 70 Years

Inclusion criteria

Inclusion criteria: 1. Age between 35-70 years old. 2. The first attack of stroke or previous luminal infarction without sequelae; 3. The diagnosis is in line with the key points of cerebrovascular disease diagnosis approved by the Fourth National Cerebrovascular Disease Academic Conference in 1995; 4. Unilateral subcortical stroke (basal ganglia, thalamus, internal capsule, etc.) confirmed by head CT or MRI; 5. Onset time >= 6 months, Brunnstrom level 0-3 of the affected hand; 6. No metal implants or pacemakers in the body; 7. No previous history of epilepsy; within good cognition does not affect communication and evaluation; 8. Able to walk at least 10m independently or with a mobility aid; 9. Informed consent is signed by the patient or his immediate family member.

Exclusion criteria

Exclusion criteria: 1. Non-conservative treatment, or skull defects; 2. Patients with Parkinson's disease or other neurological diseases; 3. Patients with serious diseases of the heart, lungs, and other organs; 4. Previous history of mental illness, drug abuse, and alcohol abuse; 5. Patients with the unstable condition, such as blood pressure indicators: low pressure = 150mmHg; 6. Strict attention, hearing, cognition, and communication disorders that can not be trained.

Design outcomes

Primary

MeasureTime frame
Broetz hand function test,BHFT;Fugl-Meyer Assessment of Upper Extremity,FMA-UE;

Secondary

MeasureTime frame
surface myoelectricity (sEMG);Modified Barthel Index;

Countries

China

Contacts

Public ContactZhou Huanxia

Shanghai Seventh People's Hospital

zhouhuanxia7@163.com+86 13641649864

Outcome results

None listed

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