Jacksonville, FLNCT07149259Now EnrollingIRB Ready

Low Vision Aids Clinical Trial in Jacksonville, FL

Access cutting-edge low vision aids treatment through this clinical trial at a research site in Jacksonville. Study-provided care at no cost to qualified participants.

Sponsored by Brooks Rehabilitation

Quick Self-Assessment

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Expert Care in Jacksonville

Access low vision aids specialists at no cost

IRB Approved

This study follows strict safety protocols and ethical guidelines

No-Cost Care

All study-related low vision aids treatment provided free

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Check if you qualify for this low vision aids clinical trial in Jacksonville, FL

Secure & Confidential

Your information is protected and will only be shared with the research team.

Why Participate?

  • No-Cost Study Care

  • Local to Jacksonville

    Convenient for FL residents

  • Cutting-Edge Treatment

    Access to innovative therapies

  • Expert Medical Care

    Close monitoring by specialists

  • Possible Compensation*

    For time and travel

*Compensation varies by study. Confirm details with coordinator.

Simple Process

  1. 1Submit this form
  2. 2Phone screening
  3. 3Visit Jacksonville site if eligible
  4. 4Begin participation

About This Low Vision Aids Study in Jacksonville

This research aims to test the updated version of Gentex's device, eSight Go, an image enhancing wearable device to assist those with vision impairments limiting activities of daily living.

Sponsor: Brooks Rehabilitation

Who Can Participate

Inclusion Criteria

Aged 18 to 90.
Best-corrected visual acuity between 20/50 to 20/400 in the better eye.
Subjects who have been diagnosed with an ocular condition causing visual impairment
Have a functional binocular field of view of at least 20 degrees.
Visual status stable for at least six months.
Demonstrate visual benefit from magnification.
Agree to wear the eSight Go in a variety of situations in the home and community.
Score ≥ 20 on the Short Orientation-Memory-Concentration Test of Cognitive Impairment (OMCT).
Subject must be able to provide an informed consent
Subject must agree to use eSight Eyewear only under conditions that will not jeopardize the safety of either the user or the device.

Exclusion Criteria

Participant must not be currently undergoing any medical or surgical procedures resulting in unstable vision.
Participants who have undergone cataract, refractive, or other surgical procedures related to vision in the six-month period prior to study enrollment.
Severe (\>20/400) visual impairment in the better seeing eye.
Cognitive limitations (\< 20 on OMCT).
Participants who have undergone any vision-related injections (e.g. anti-VEGF) in the two-month period prior to the study because of active bleeding in the retina. Ongoing anti-VEGF treatments are permitted if the participant is in a "Treat and Extend" or pro re nata ("PRN") disease management, and macula is dry.
Participants are unable or unwilling to adhere to the examination schedules as they are described in the study protocol. This may also include participants already enrolled, who for whatever reason, have become unable or unwilling to continue the study. This may also include participants for whom the travel time to/from the study site is unacceptable.
Participants who self-report a history of alcoholism, drug abuse, or psychosis.
Participants who exhibit clinical evidence of depression, poor motivation, emotional or intellectual problems, or any other conditions which would likely limit validity of consent or appropriate responses to participate in the study or who are deemed unsuitable psychologically or physiologically for study participation by the investigator.
Participants who may have a conflict of interest with eSight Corp, which could reasonably influence their participation in the study.
Refractive error outside the range correctable by lens inserts in the device (\> +/-8.00 D sph or -4.00 cyl)

Not sure if you qualify? Submit your interest and a study coordinator will help determine your eligibility.

Frequently Asked Questions

Q:Is this study available in Jacksonville?

Yes, this clinical trial (NCT07149259) has an active research site in Jacksonville, FL that is currently enrolling participants.

Q:Is it safe to participate?

Clinical trials follow strict safety guidelines and ethical standards. This study has been reviewed and approved, and participants are closely monitored by medical professionals. You can withdraw at any time.

Q:Will I be compensated?

Many clinical trials offer compensation for your time and travel expenses. Specific compensation details will be discussed during the screening process. All study-related medical care is provided at no cost.

Q:Can I leave the trial if I change my mind?

Absolutely. Participation is completely voluntary. You have the right to withdraw from the study at any time, for any reason, without penalty.

Still have questions? Our study coordinators are here to help.

Low Vision Aids Treatment Options in Jacksonville, FL

If you're searching for low vision aids treatment options in Jacksonville, FL, this clinical trial (NCT07149259) may be an excellent opportunity. Clinical trials provide access to cutting-edge treatments that aren't yet available to the general public, often at no cost to participants.

Our Jacksonville research site is actively enrolling participants for this clinical trial. You'll receive care from experienced low vision aids specialists who are at the forefront of medical research. All study-related care, including examinations, treatments, and monitoring, is provided at no cost to qualified participants.

Looking for more options? Browse all low vision aids clinical trials near you to find additional studies recruiting in your area.

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Secure · Expert Care · Jacksonville, FL