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Comparison of Concentric or Eccentric Virtual Reality Training Program in Subacute-stroke Patients With Hemispatial Neglect

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Yonsei University

Status

Unknown

Conditions

Stroke
Neglect

Treatments

Device: efferent virtual reality program
Device: afferent virtual reality program

Study type

Interventional

Funder types

Other

Identifiers

NCT04651335
4-2012-0416

Details and patient eligibility

About

The purpose of this study is to compare and analyze how the visual gaze training in the afferent direction and the visual gaze training in the efferent direction using virtual reality affects the improvement of the neglect phenomenon in patients with subacute stroke with unilateral neglect.

Based on the behavioral intention test (BIT) test and the Mini-Mental Screening Examination test (MMSE) test for the group of unilateral neglected patients with stroke findings among all eligible patients for this experiment.

Appropriate subjects are selected and randomly divided into two groups. One group uses an afferent virtual reality program, and the other uses an efferent virtual reality program to train five times a week for a total of 4 weeks.

Before training, a computer experience scale 21 was additionally performed, and to find out the degree of unilateral negligence, evaluation was performed using the Behavioral Inattention Test (BIT) and Catherine Bergego Scale (CBS)22, and the angle of deflection (deviation angle), out-of-focus time, gaze time, failure rate, and head rotation trajectory were evaluated. In addition, reaction time, failure rate, and head rotation trajectory were evaluated using a virtual reality program (Assessment program-V2) to evaluate the degree of unilateral negligence. After that, BIT, CBS, and Assessment program-V2 tests are performed to determine the degree of improvement in visual ignorance due to each program.

Enrollment

44 estimated patients

Sex

All

Ages

18 to 120 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  1. A person with left hemiplegia who was found to have a stroke by MRI or CT.
  2. A person who has been confirmed to have unilateral neglect (BIT 196 or less, or each subtest cut off or less)
  3. A person who has enough cognitive ability to receive virtual reality training. (In case of more than 20 points in MMSE)
  4. Those within 3 months of onset.

Exclusion criteria

  1. Those with a history of recurring brain damage
  2. hemianopsia
  3. When there is a disorder in the movement of the neck due to orthopedic problems
  4. Someone has vision and hearing problems during evaluation and treatment
  5. difficult to maintain a sitting position in a chair with back and armrests
  6. other diseases that may affect your general cognitive decline
  7. who disagree with this study

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

44 participants in 2 patient groups

Concentric
Active Comparator group
Description:
uses an afferent virtual reality program
Treatment:
Device: afferent virtual reality program
Eccentric
Active Comparator group
Description:
uses an efferent virtual reality program
Treatment:
Device: efferent virtual reality program

Trial contacts and locations

1

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Central trial contact

Deog Young Kim

Data sourced from clinicaltrials.gov

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