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Clinical Trials in Canada / NCT05397873
Recruiting Not applicable

Biofeedback for Hemianopia Vision Rehabilitation

NCT05397873 · tracked via the Priya Life Science Canada tracker
Phase
Not applicable
Started
2021-12-01
Last updated
2025-05-09

Condition(s) studied

Hemianopsia, HomonymousBrain InjuryStrokeBrain TumorBrain Trauma

Investigational drug(s) / intervention(s)

Biofeedback training

Biofeedback training: The training of oculomotor functions is done on the biofeedback module of a microperimeter MAIA.

Study summary

Patients with brain injury secondary to stroke, surgery, or trauma frequently suffer from homonymous hemianopia, defined as vision loss in one hemifield secondary to retro- chiasmal lesion. Classic and effective saccadic compensatory training therapies are current aim to reorganize the control of visual information processing and eye movements or, in other words, to induce or improve oculomotor adaptation to visual field loss. Patients learn to intentionally shift their eyes and, thus, their visual field border, into the area corresponding to their blind visual field. This shift brings the visual information from the blind hemifield into the seeing hemifield for further processing. Patients learn, therefore, to efficiently use their eyes "to keep the 'blind side' in sight". Biofeedback training (BT) is the latest and newest technique for oculomotor control training in cases with low vision when using available modules in the new microperimetry instruments. Studies in the literature highlighted positive benefits from using BT in a variety of central vision loss, nystagmus cases, and others.The purpose of this study is to assess systematically the impact of BT in a series of cases with hemianopia and formulate guidelines for further use of this intervention in vision rehabilitation of hemianopia cases in general.

Eligibility

Sex
ALL
Min age
18 Years
Max age
90 Years
Healthy volunteers
No
Inclusion Criteria: * hemianopia cases previously diagnosed accordingly by microperimetry and other tests as needed * 18-90 years old * ability to follow the visual and auditory stimuli and training instructions Exclusion Criteria: * previous or current treatment for low vision rehabilitation * ocular diseases * other serious clinical conditions not related to the hemianopia physiopathology * both eyes with media opacity that impairs microperimetry testing * lack of ability to perform the tests and training

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
Toronto Western Hospital Toronto Ontario Recruiting

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Other trials for the same condition

Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT05397873 on ClinicalTrials.gov ↗ ← All trials in Canada