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Immersive Virtual Reality Based Training for Rehabilitation of Subacute Stroke

S

Second Affiliated Hospital of Wenzhou Medical University

Status

Terminated

Conditions

Immersion Virtual Reality Training ,Stroke, Upper Extremity, Randomized Controlled Trial

Treatments

Other: traditional rehabilitation training
Other: immersion virtual reality (VR)-based rehabilitation

Study type

Interventional

Funder types

Other

Identifiers

NCT03086889
KFYXK001

Details and patient eligibility

About

The investigators will conduct a single-blind, randomized controlled trial of 60 patients with subacute stroke. Patients will be randomly assigned into a control group and an intervention group. The intervention group will participate in immersion VR training for 3 weeks. The control group will receive for traditional rehabilitation training for 3 weeks. Then, the patients will be reevaluated to determine changes in upper extremity function, cognitive function, cortical and subcortical activation patterns, and performance of activities of daily living after the baseline assessment.

Enrollment

40 patients

Sex

All

Ages

30 to 80 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  1. having had an ischemic stroke in the first time
  2. age 30 to 80 years old
  3. first stroke within 2 month
  4. GCS score >8
  5. the upper-limb function BrunnstromⅡ、Ⅲ

Exclusion criteria

  1. hemorrhage or transient ischemic attack(TIA)
  2. important organs such as heart, lung, liver, kidney function decline or failure
  3. previous history of brain neurosurgery or epilepsy
  4. had severe cognitive impairments or aphasia, which made the participants unable to understand the instructions given by the investigators
  5. with claustrophobia and body with metal (such as metal teeth, etc.) are not suitable for to MRI scanning

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Single Blind

40 participants in 2 patient groups

The intervention group
Experimental group
Description:
The intervention group will participate in immersion virtual reality based rehabilitation training for 3 weeks.
Treatment:
Other: immersion virtual reality (VR)-based rehabilitation
The control group
Other group
Description:
The control group will receive for traditional rehabilitation training for 3 weeks.
Treatment:
Other: traditional rehabilitation training

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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