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RECRUITING NA

Eye Recovery Automation for Post Injury Dysfunction (iRAPID)

NCT06105892 · View on ClinicalTrials.gov ↗

Study Summary

This study will test a portable virtual reality (VR) system with integrated eye tracking called Virtual Eye Rotation Vision Exercises (VERVE). The proposed VERVE platform will deliver vergence therapy in an automated manner. This research will involve 30 non-traumatic brain injury (TBI) binocularly normal (BNC) Veterans and 50 post-traumatic convergence insufficiency (PTCI) Veterans who will undergo Active and Sham therapy (equally divided groups) to determine the effectiveness of VERVE vergence therapy.

Interventions

  • DEVICE Virtual Eye Rotation Vision Exercise (VERVE)
  • DEVICE Sham VR Therapy

Study Locations (1)

New Mexico

  • New Mexico VA Health Care System — Albuquerque

Trial Details

FieldValue
Enrollment Target 100 participants
Start Date 2023-10-23
Est. Completion 2027-03-20
Phase NA

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Full Details on ClinicalTrials.gov ↗

What the Registry Record Tells You About NCT06105892

The ClinicalTrials.gov registry entry for NCT06105892 describes a study currently listed as recruiting. It is categorized as NA, which is the standard way researchers label where a study sits along the investigational pathway from early safety work through later efficacy and post-marketing evaluation. The registered enrollment target is 100 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is New Jersey Institute of Technology, which has 3 total studies on file at ClinicalTrials.gov, and sponsors are the parties responsible for study design, oversight, and regulatory filings.

The record links to 3 conditions, with Traumatic Brain Injury appearing as the primary indexed condition, and to 2 interventions — of which Virtual Eye Rotation Vision Exercise (VERVE) is the first listed. Interventions can include drugs, devices, procedures, behavioral programs, or observational arms, and each is tracked as a separate registry field so that downstream queries can filter accurately. When a trial lists multiple interventions, it usually reflects a multi-arm design or a comparison protocol rather than a single treatment being tested in isolation. The brief summary published in the registry is the clearest source of protocol intent and should be read before drawing conclusions from any sidebar tags.

Geographic footprint matters for practical reasons: NCT06105892 reports 1 study location spanning 1 distinct geographic area — top geographies include New Mexico. A larger site network tends to correlate with broader recruitment capacity, but it does not imply anything about study quality, and site-level enrollment status can diverge from the overall registry status shown above. Every data point on this page comes from the public ClinicalTrials.gov dataset and is reproduced here for reference only; it is not a medical recommendation, an endorsement of the sponsor, or an invitation to enroll. Verify current status, eligibility criteria, and contact details directly at ClinicalTrials.gov, and discuss any participation decision with your own healthcare provider.

Frequently Asked Questions

What is clinical trial NCT06105892 about?

NCT06105892 is a clinical study titled "Eye Recovery Automation for Post Injury Dysfunction (iRAPID)". This study will test a portable virtual reality (VR) system with integrated eye tracking called Virtual Eye Rotation Vision Exercises (VERVE). The proposed VERVE platform will deliver vergence therapy in an automated manner. This research will involve 30 non-traumatic brain injury (TBI) binocularly ...

What is the current status of trial NCT06105892?

This trial is currently recruiting. It is a NA study. The enrollment target is 100 participants. The study started on 2023-10-23. Estimated completion is 2027-03-20.

What conditions does trial NCT06105892 study?

This clinical trial studies the following conditions: Traumatic Brain Injury, Concussion, Mild, Convergence Insufficiency. These conditions were identified from the trial registry and reflect the primary focus areas of the research.

What interventions are being tested in trial NCT06105892?

The interventions under investigation include: Virtual Eye Rotation Vision Exercise (VERVE) (DEVICE), Sham VR Therapy (DEVICE). Each intervention is being evaluated for safety and efficacy as part of this clinical study.

Who is sponsoring clinical trial NCT06105892?

This trial is sponsored by New Jersey Institute of Technology, which has 3 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.

Where is trial NCT06105892 being conducted?

This trial has 1 study location across New Mexico. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

Related

Data sourced from official U.S. government datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial