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Effectiveness of Virtual Reality and Exoskeleton Robot-based in the Hand Function Rehabilitation of Stroke Patients

Effectiveness of Virtual Reality and Exoskeleton Robot-based in the Hand Function Rehabilitation of Stroke Patients

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500098712
Enrollment
Unknown
Registered
2025-03-12
Start date
2025-03-20
Completion date
Unknown
Last updated
2025-03-17

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

Conditions

Stroke

Interventions

The treatment group of virtual reality combined with exoskeleton robots:Receive traditional physical therapy and occupational therapy, 1 hour per day, 5 days a week for a total of 4 weeks. At the same
The mirror therapy group:Receive traditional physical therapy and occupational therapy, 1 hour per day, 5 days a week for a total of 4 weeks. At the same time, receive mirror therapy training for 30 m

Sponsors

Chinese PLA General Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: 1. Unilateral lesion with a clear CT or MRI diagnosis. 2. Age>=18 years. 3. Simple motor dysfunction, the proximal Brunnstrom stage of the upper limb on the affected side is stage II-IV. 4. Have certain cognitive ability, Mini-mental State Examination (MMSE) score: middle school or above>=22 points; Primary > = 20 points; Primary > = 17 points. 5. The patient's vision is not significantly impaired, and he can understand visual information.

Exclusion criteria

Exclusion criteria: 1. Patients with Alzheimer's disease and decreased comprehension. 2. Patients with severe anxiety and depression. 3. Patients with severe impairment of auditory and auditory senses. 4. Patients with motor dysfunction of both upper limbs caused by bilateral brain injury. 5. Patients with good recovery of motor function and Brunnstrom stage IV or above. 6. Patients with severe shoulder pain, fracture and surgery on the affected side of the upper limb. 7. Those who are undergoing other clinical investigations.

Design outcomes

Primary

MeasureTime frame
Fugl-Meyer assessment scale for upper extremity, FMA-UE score;

Secondary

MeasureTime frame
Nine Hole Peg Test Score;Functional Independence;Brunnstrom Assessment of Hand Function Grading;Barycentric value, slope value and mean value of changes in oxygenated hemoglobin;Electroencephalogram (EEG) change;

Countries

China

Contacts

Public ContactLiping Huang

Chinese PLA General Hospital

ping-online@163.com+86 133 9190 8450

Outcome results

None listed

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