Medical Information Only. Always consult your healthcare provider before enrolling in any clinical trial.

NCT05098236 · ClinicalTrials.gov registry record · NA

Effect of Visual Retraining on Visual Loss Following Visual Cortical Damage

A NA study, sponsored by University of Rochester.

Completed
Registry status
NA
Development phase
280
Enrollment target

NCT05098236: Completed NA study, sponsored by University of Rochester.

NCT05098236 is a NA study that has completed, run by University of Rochester. The registered enrollment target is 280 participants, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (80% lower). According to ClinicalTrials.gov, the official US trial registry.

View on ClinicalTrials.gov ↗

View your shortlist →

The verdict

NCT05098236, a NA study, has completed, sponsored by University of Rochester.

COMPLETED
Registry status
NA
Development phase
280 participants
Enrollment target

Study Summary

This project is intended to collect data using standard clinical tests and psychophysics to quantify the effect of visual cortical damage on the structure of the residual visual system, visual perception, spatial awareness, and brain function. The investigators will also assess the effect of intensive visual retraining on the residual visual system, processing of visual information and the use of such information in real-world situations following damage. This research is intended to improve our understanding of the consequences of permanent visual system damage in humans, of methods that can be used to reverse visual loss, and of brain mechanisms by which visual recovery is achieved.

Primary Outcome

For each subject, the investigators will measure the change in ability to detect differences in the motion direction of visual stimuli relative to horizontal, measured in degrees of visual angle. These assessments will be based on what can be reliably detected at a 72-75% correct level of performance. These measures of change will be evaluated baseline and at each subsequent visit to the laboratory; minimally from baseline to 4-months, then baseline to 12-months from start of training.

Interventions

  • OTHER Training in the Blind Field
  • OTHER Training in the Sighted Field

Trial Details

FieldValue
Enrollment Target 280 participants
Start Date 2003-09-26
Est. Completion 2024-06-04
Phase NA
University of Rochester

636 total trials

What the finished NCT05098236 record still lists

NCT05098236 is an interventional study that assigns participants to a tested intervention. The registered 280 participants enrollment target is mid-sized for trials with a published cap, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (80% lower).

The record links to 0 conditions, and to 2 interventions - of which Training in the Blind Field is the first listed.

NCT05098236 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT05098236 about?

NCT05098236 is a clinical study titled "Effect of Visual Retraining on Visual Loss Following Visual Cortical Damage". This project is intended to collect data using standard clinical tests and psychophysics to quantify the effect of visual cortical damage on the structure of the residual visual system, visual perception, spatial awareness, and brain function. The investigators will also assess the effect of intensi...

What is the current status of trial NCT05098236?

This trial is currently completed. It is a NA study. The enrollment target is 280 participants. The study started on 2003-09-26. Estimated completion is 2024-06-04.

What interventions are being tested in trial NCT05098236?

The interventions under investigation include: Training in the Blind Field (OTHER), Training in the Sighted Field (OTHER).

Who is sponsoring clinical trial NCT05098236?

This trial is sponsored by University of Rochester, which has 636 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT05098236's enrollment target sits among peer trials

280 380th of 2000 higher than 1,620 of 2,000 other NA trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other NA trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.

Source ClinicalTrials.gov registry export · 2026-08-08

Nationwide trials with similar profiles

Cross-condition peers matched on enrollment target and registry start date, not the same-condition list above.

Similar enrollment target

  • NCT04084730 · 280 participants · Phase 2

    Study of 3-Day Partial Breast Radiation Therapy in Women With Breast Cancer

  • NCT04518657 · 280 participants · NA

    Internet-Delivered Lifestyle Physical Activity Intervention for Cognitive Processing Speed in Multiple Sclerosis

  • NCT04634916 · 280 participants · NA

    Post-market Surveillance Study of the BD® WavelinQ™ EndoAVF System

  • NCT04829617 · 280 participants · NA

    Promoting Well-being and Health in Heart Failure

Similar registry start date

  • NCT05962346 · started 2026-12 · NA

    Fetal Endoscopic Tracheal Occlusion for Congenital Diaphragmatic Hernia

  • NCT07125183 · started 2026-12 · Phase 2

    Study on Efficacy and Tolerability of Weekly Doxorubicin in Elderly Patients With Advanced or Metastatic Leiomyosarcoma

  • NCT07292298 · started 2026-11 · Phase 2

    Phase 2 Single-Arm Rectal Cancer Brachytherapy for Patients With Low-Lying Residual Adenocarcinoma After Total Neoadjuvant Therapy to Improve Organ Preservation Rates

  • NCT04263285 · started 2026-10 · NA

    Treatment of Depression Post-SCI

Source: ClinicalTrials.gov NCT05098236, the US trial registry maintained by the National Library of Medicine. NCT05098236 (mid enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.