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NCT05525949Completed

Visual Perceptual Learning Based Digital Therapeutics for Visual Field Defect After Stroke

Treatment of Homonymous Visual Loss With Digital Therapeutics, VIVID Brain, Visual Perceptual Learning Device (HOGWAND Trial) : Multi Center, Randomized, Single-blind (Evaluator), Superiority Prove, Prospective Confirmatory Trial

Source: ClinicalTrials.gov · Last updated 13 Nov 2023

Brief summary (registry, in English)

This study evaluates the efficacy of visual perceptual learning for the treatment of visual field defect caused by brain disease. Half of participants will receive visual perceptual training using the VIVID Brain. The other half will not receive any training because there is no standard treatment for visual field defect caused by brain disease.

Status (registry)
Completed
Study type
Interventional
Enrollment
93 (actual)
First submitted
31 Aug 2022
Start date
19 Oct 2022
Primary completion date
11 Aug 2023
Lead sponsor
Nunaps Inc
Diseases
Stroke
NCT number
NCT05525949

What you commit to

  • Study type: Interventional
  • Participants enrolled: 93
  • From 19 Oct 2022 to the primary completion date, 11 Aug 2023
  • 12 sites in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • Received ophthalmologic surgery or laser surgery within 3 months, except for the cataract surgery

Other illness

  • Epilepsy, photosensitivity, Parkinson's disease
  • Ophthalmologic disorder that may interfere the trial. (Ptosis of Eyelid, Corneal Opacity, Diabetic Retinopathy, Glaucoma, Macular Degeneration etc.)
  • Any other condition that, in the opinion of the investigator, precludes participation in the trial

Other

  • Complete hemianopsia
  • Bilateral visual field defect
  • Hemispatial neglect
  • Inability to discontinue psychostimulants such as methylphenidate, modafinil, and amphetamine.
  • Candidate for carotid endarterectomy or stenting
  • Pregnant or breast feeding
  • Participating in other clinical trial

Who the study is looking for

  • 19 years and older
  • At least 3 months after brain disease related to visual field defect
  • Verified brain disease in visual pathway related to occipital lobe, parietal lobe, temporal lobe or etc. using CT or MRI
  • Brain disease induced visual field defect
  • Able to use the VR(Virtual Reality) device
  • Able to use the app with a smart phone
  • Patient/legally authorized representative has signed the informed consent form

Age in the registry: 19 years to - · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (12)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Korea University Ansan Hospital
Coordinator of this site? Confirm its status
AnsanSouth KoreaUnknown status
Hallym University Sacred Heart Hospital
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AnyangSouth KoreaUnknown status
Daejeon Eulji University Medical Center
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DaejeonSouth KoreaUnknown status
Inje University Ilsan Paik Hospital
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GoyangSouth KoreaUnknown status
Seoul National University Bundang Hospital
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SeongnamSouth KoreaUnknown status
Samsung Medical Center
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SeoulSouth KoreaUnknown status
Chung ang University Hospital
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SeoulSouth KoreaUnknown status
The Catholic University of Korea Yeouido St. Mary's Hospital
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SeoulSouth KoreaUnknown status
The Catholic University of Korea, Seoul ST. Mary's Hospital
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SeoulSouth KoreaUnknown status
Asan Medical Center
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SeoulSouth KoreaUnknown status
Konkuk University Hospital
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SeoulSouth KoreaUnknown status
Ulsan University Hospital
Coordinator of this site? Confirm its status
UlsanSouth KoreaUnknown status

This page is information, not medical advice. Discuss any trial with your doctor.