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Behavioural Intervention

VR System for Cross-modal Rehabilitation of Hemianopia

N/A
Waitlist Available
Led By Huai Jiang, PhD
Research Sponsored by Wake Forest University Health Sciences
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial
Must have
* Adult volunteers diagnosed with homonymous visual hemianopia / hemianopsia (ages 18-99)
Be older than 18 years old
Timeline
Screening 3 weeks
Treatment Varies
Follow Up baseline, 2 months, 3 months
Awards & highlights
No Placebo-Only Group

Summary

The purpose of this research study is to investigate the effectiveness of a new rehabilitation for visual hemianopia. The study team believes a cross-modal rehabilitation technique delivered by a virtual reality system can help restore the visual field for subjects with homonymous hemianopia.

Eligible Conditions
  • Homonymous Hemianopia

Eligibility Criteria

Inclusion Criteria

You may be eligible if you check “Yes” for the criteria below

Timeline

Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~baseline, 2 months, 3 months
This trial's timeline: 3 weeks for screening, Varies for treatment, and baseline, 2 months, 3 months for reporting.

Treatment Details

Study Objectives

Study objectives can provide a clearer picture of what you can expect from a treatment.
Primary study objectives
Humphrey Visual Field Perimetry
Peripheral Visual Field Frame Test
Virtual Reality (VR) Visual Field Test--Mean Percent Correct
+1 more
Secondary study objectives
NEI-VFQ-25--Color Vision Score Subscale
NEI-VFQ-25--Composite Score
NEI-VFQ-25--Dependency Score Subscale
+15 more
Other study objectives
Color Vision Test
Grating Acuity Test
Shape Recognition Test

Awards & Highlights

No Placebo-Only Group
All patients enrolled in this study will receive some form of active treatment.

Trial Design

1Treatment groups
Experimental Treatment
Group I: Experimental Group Virtual Reality (VR) TreatmentExperimental Treatment1 Intervention
Visual Auditory Virtual Reality rehabilitation for visual hemianopia
Treatment
First Studied
Drug Approval Stage
How many patients have taken this drug
Cross-model Visual Auditory Rehabilitation
2020
N/A
~10

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Who is running the clinical trial?

Wake Forest University Health SciencesLead Sponsor
1,397 Previous Clinical Trials
2,460,123 Total Patients Enrolled
Huai Jiang, PhDPrincipal InvestigatorWake Forest University Health Sciences
~1 spots leftby Dec 2025
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