Assessing the Impact of eSight Go At-Home Usage in Individuals With Visual Impairment

Conditions

• Low Vision Aids

Eligibility Criteria

Sex

ALL

Age

18 Years - 90 Years

Healthy Volunteers

Not accepted

Interventions

• At Home Use — DEVICE
  Participants will take the device home for 4 weeks to use in daily living, such as the home and community settings. There will be regular follow-up phone calls once per week from a member of the research team (e.g., an occupational therapist, or low vision therapist) who is familiar with the device to assist with possible troubleshooting as well as device use strategies. The follow up calls will also collect information about device use time and activities. The device will be returned at visit 2.

Study Details

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.

Key Dates

Start date

Jun 18, 2025

Status verified

Aug 2025

Primary completion

Jun 1, 2026

Completion

Jun 1, 2026

Study Design

Enrollment

50 participants (estimated)

Allocation

NA

Intervention model

SINGLE_GROUP

Primary purpose

TREATMENT

Arms

• Experimental: At Home Device Utilization
  eSight Go device will be utilized at home for a total of 4 weeks in environments the participant feels comfortable using it (e.g. home, work, stores).

Primary Outcome Measure

Change in Visual Acuity [ Time Frame: Pre-intervention and post-intervention at 4 weeks ]

Central Contacts

• Hannah Grimes
  904-597-3478
  [email protected]

Locations (1)

Find similar trials in Jacksonville, FL

Related Studies

• Beacon Sensors and Telerehabilitation to Assess and Improve Use of Devices (BeST-AID) for Low Vision
  Recruiting · University of California, Los Angeles · Fullerton, California