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Completed

NCT Number: NCT03444961

Computer-Assisted Rehabilitation Environment Training After Argus Retinal Prosthesis

The goal of the current project is to fill the unmet clinical needs around the objective assessment of visual function and develop outcome-oriented visual rehabilitation approach using the computer assisted rehabilitation environment (CAREN) system for Argus recipients.

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Key information

Age range

25 year–100 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Cleveland Clinic

Cleveland, Ohio, 44195, United States

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Recipient of the Argus II Retinal Prosthesis System
  • Ability to provide informed consent
  • Ability to follow two-step commands
  • Ability to ambulate 300+ feet with or without visual assistance
  • Able to tolerate Argus device turned on for >20 continuous minutes.

Exclusion criteria

  • Dementia
  • Musculoskeletal contraindication to exercise or walking
  • Cardiopulmonary contraindication exercise (i.e. uncontrolled heart failure, cardiac arrhythmia, or pulmonary disease).

Treatment and study plan

CAREN system training

Device

CAREN allows Argus users to be trained and enhance their device usage in a safe, controlled, and standardized environment.

Primary outcomes

  1. Effects of CAREN Virtual Reality System on Obstacle Course Navigation

    Time frame: 6 wks

    Obstacle course navigation - time (seconds) to complete an obstacle course (walking forward while navigating over a ramp and curb)

  2. Time to Complete the Timed Up and Go Test Before and After CAREN Virtual Reality System Training

    Time frame: 6 wks

    Timed Up and Go testing - functional mobility test that requires the individual to stand from a chair, ambulate three meters to a target, turn around, return to the chair, and sit down. Participants were asked to complete two trials was recorded, with a maximum time of 60 seconds per trial.

  3. Effects of CAREN Virtual Reality System on Square Localization Visual Function Test

    Time frame: 6 wks

    The square localization test presents a 2.75" square (250 pixels) at a random location on a black background and the patient is instructed to try to touch the square. The test measures the patient's ability to locate an object and results are calculated as a mean error (how far away in pixels from the square the patient touches the screen). A lower mean error (the distance from the square) indicates better patient performance.

  4. Effects of CAREN Virtual Reality System on Direction of Motion Visual Function Test.

    Time frame: 6 wks

    The direction of motion test assesses the patient's ability to determine the direction an object is moving. The patient is presented with a white line (1.4'' wide) that moves across the screen in a random series of directions and angles. Patients are instructed to trace their finger on the monitor in the direction they perceived the line moved. Results are calculated as a mean error (how far off, in degrees, was the patient from the direction of the moving line). The higher the mean error/score, the worse the outcome.

  5. Effects of CAREN Virtual Reality System on Grating Visual Acuity Visual Function Test

    Time frame: 6 wks

    The grating visual acuity test measures the patient's visual acuity using the principles of acuity charts modified for ultra-low vision subjects. The patients are presented with black and white bars in one of four orientations (horizontal, vertical, diagonal to the left or diagonal to the right). The bars are present on the screen for 5 seconds during which the patient may scan the screen and then provide a verbal response as to which orientation they perceived the bars. The widths of the bars are varied to evaluate different levels of visual acuity. A lower score is associated with better outcomes with 2.9 being the worst possible score.

  6. Effects of CAREN Virtual Reality System on Gait Assessment

    Time frame: 6 wks

    Subject's gait assessed by meters traveled while localizing objects on the CAREN system. The higher scores are associated with better outcomes (further distance walked).

Other outcomes

  1. Effects of CAREN Virtual Reality System on Activities-specific Balance Confidence (ABC) Scale Questionnaire

    Time frame: 6 wks

    The Activities-specific Balance Confidence Scale (ABC Scale) is a structured questionnaire that measures an individual's confidence in performing activities without losing balance. It is a 0% to 100% continuous response scale with 0 representing "no confidence" and 100 representing "complete confidence."

Sponsors and collaborators

Lead sponsor

The Cleveland Clinic

Other

Registry information

Official study title

Comprehensive Visual and Mobility Training Using Computer-Assisted Rehabilitation Environment (CAREN) After Argus Retinal Prosthesis Surgery

Important dates

Study start
2018
Primary completion
2018
Study completion
2018
First posted
Feb 26, 2018
Registry last updated
Jul 14, 2021

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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