Actively Recruiting

Phase Not Applicable
Age: 18Years +
All Genders
ID07105358

Vision Improvement Through Behavioral Rehabilitation And Neuroplasticity Training

Led by Georgetown University · Updated on 2025-08-05

30

Participants Needed

1

Research Sites

N/A

Total Duration

On this page

AI-Summary

What this Trial Is About

Researchers are investigating visual improvements in people with homonymous hemianopia, a type of vision loss caused by damage to the brain's visual pathways. This study explores whether combining transcranial random noise stimulation (tRNS) with training based on perceptual learning can help improve visual impairments. The study uses a double-blind, randomized crossover design to compare these approaches within the same participants. Participants will attend sessions where they receive either active tRNS or sham stimulation applied to the bilateral human middle temporal complex (hMT+), paired with a motion discrimination training task. Each session lasts two days and includes up to three 18-minute stimulation periods combined with perceptual learning exercises. The sham stimulation mimics the active treatment with a brief ramp-up period but no ongoing current. The study includes both focal brain damage patients and healthy volunteers as controls. During the study, participants will be assessed for changes in their ability to discriminate motion shortly after treatment sessions, as well as changes in their visual field, visual perception, and quality of life up to six months later. Researchers will monitor adherence to training and collect data on visual improvements and life impacts. The total participation time includes initial visits, intervention sessions, and follow-ups to evaluate lasting effects.

CONDITIONS

Brief Title

Visual Plasticity Following Brain Lesions

Who Can Participate

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • At least 18 years old.
  • Able to provide informed consent and follow study procedures.
  • For patients: unilateral or bilateral focal brain damage causing vision loss.
  • For patients: at least 3 months past stroke or traumatic brain injury, or stable brain tumor within past year.
  • For healthy volunteers: age-matched adults able to consent and comply with study procedures.
Not Eligible

You will not qualify if you...

  • Severe central nervous system diseases unrelated to brain lesion.
  • Severe mental health challenges or drug/alcohol abuse within past 6 months.
  • Vision loss caused by eye diseases or disorders.
  • Healthy volunteers with CNS diseases, psychiatric disorders, previous head injury, or recent substance abuse.

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

1 visit (in-person)

Treatment

Duration - Each session lasts 2 days, with two sessions separated by a washout period.

Participants undergo two 2-day sessions where they receive either transcranial random noise stimulation (tRNS) or sham stimulation paired with perceptual learning-based training involving motion discrimination tasks.

Up to 6 visits (in-person) for stimulation and training

Follow-up

Duration - Approximately 3 to 6 months

Participants are monitored for changes in visual field, visual perception, and quality of life after the intervention.

1 to 2 visits depending on assessments

Trial Site Locations

Total: 1 location

1

Georgetown University Medical Center

Washington D.C., District of Columbia, United States, 20057

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Research Team

T

Tina Liu, PhD

K

Kyungji Moon, MS

How is the study designed?

Study Type

INTERVENTIONAL

Masking

DOUBLE

Allocation

RANDOMIZED

Model

CROSSOVER

Primary Purpose

TREATMENT

Number of Arms

2

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