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Study on the clinical application, norms, and standards of virtual reality rehabilitation training system for sensory-daily activities ability

Study on the clinical application, norms, and standards of virtual reality rehabilitation training system for sensory-daily activities ability

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2100052540
Enrollment
Unknown
Registered
2021-10-30
Start date
2021-10-18
Completion date
Unknown
Last updated
2022-10-17

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

Conditions

Stroke

Interventions

experimental group:conventional sensory rehabilitation training + NeuCir-VR

Sponsors

Shanghai University of Traditional Chinese Medicine
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 70 Years

Inclusion criteria

Inclusion criteria: 1. Patients diagnosed with stroke by clinical assessment and comprehensive imaging examination met the diagnostic criteria for stroke; 2. Fugl-Meyer sensory function score proved to be sensory dysfunction (below 24 points); 3. Aged 18 to 70 years, no gender limit; 4. No cognitive impairment or communication impairment, with a mini-mental state examination (MMSE) score of 27 or more; 5. The first onset, the duration of the disease was less than 6 months.

Exclusion criteria

Exclusion criteria: 1. Those who have serious systemic diseases such as cardiopulmonary disease and cannot tolerate rehabilitation treatment; 2. Patients with diagnosed psychosis, major depression (suicidal tendency) or epilepsy, and those with a family history of psychosis or epilepsy; 3. There are influencing factors of serious systemic diseases such as diabetes and uremia; 4. According to the safety guidelines, there are contraindications for transcranial direct current/magnetic stimulation (TMS/tDCS) and functional magnetic resonance (fMRI) examinations such as metal foreign bodies in the body or other electronic devices implanted in the body, etc.; 5. Defects in hearing or vision may affect assessment and virtual reality rehabilitation; 6. Use drugs that change the excitability of the cerebral cortex (antiepileptic drugs, sedative, and hypnotic drugs, etc.).

Design outcomes

Primary

MeasureTime frame
change of Fugl-meyer sensory function score;

Secondary

MeasureTime frame
Tactile threshold of the upper/lower limbs of the affected side;Two-point discrimination of the upper/lower limbs of the affected side;Upper/lower limb sensory index score of the affected side;evaluation of the joint position and motion direction of the affected upper/lower limbs;Electrophysiological examination of upper and lower limbs of affected side;Fugl-meyer balance function score;the functional magnetic resonance imaging (fMRI);mini-mental state examination;modified Ashworth score;Daily life (behavior) ability;

Countries

China

Contacts

Public ContactXu Jianguang

Shanghai University of Traditional Chinese Medicine

xjg@shutcm.edu.cn+86 21 51322091

Outcome results

None listed

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