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V-NAV Usability Study: End Users Trying the Vortant Indoor Navigation Tool

V

Vortant Technologies, LLC

Status

Suspended

Conditions

Blindness and Low Vision

Treatments

Other: V-NAV indoor navigation prototype

Study type

Interventional

Funder types

Other

Identifiers

NCT05647694
NEI-VNAV-2C

Details and patient eligibility

About

The study will begin with an explanatory/training session where individuals with low vision will learn to use the V-NAV (Vortant NAVigation tool) indoor navigation app, and will have the opportunity to try it for a few representative tasks. The main activity includes a take-home trial, an extended unstructured period to emulate the post-purchase experience of users, during which participants will have the opportunity to use the V-NAV in their everyday lives. Data will be collected from the users to measure the relative advantage of V-NAV compared to the user's current indoor navigation method.

Full description

The introductory session, emphasizing real-world experiences, will involve a brief training session followed by simulated navigation experiences in a convenient location to the users. Participants will use V-NAV to record approximately 8 locations, then will be given instructions to find these locations again. The V-NAV prototype's logging software will measure distance walked and task time. Participants will complete a study-specific tool covering the relevant attributes of the V-NAV prototype, as well as a standardized tool, the NASA TLX (Task Load Index).

Subsequently, participants will complete a take-home trial, during which they will be encouraged to use the V-NAV features regularly to support their everyday community navigation activities. Participants will be contacted approximately weekly with a "check-in" to answer questions and resolve any emergent technical problems. At the conclusion of the trial, a product-specific tool and an appropriate standardized tool, the PIADS (Psychosocial Impact of Assistive Devices Scale) will be administered.

Enrollment

16 estimated patients

Sex

All

Ages

12+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • AFB "visually impaired" definition, acuity 20/70 or worse or field loss of 140 degrees

Exclusion criteria

  • Any health condition that may affect safety of individual to participate
  • Any physical, mental, or behavioral impairment that would provide more than minimal risk or hindering ability to comprehend the purpose of the device or otherwise to be a potential user of the V-NAV hardware or app.

Trial design

Primary purpose

Other

Allocation

N/A

Interventional model

Single Group Assignment

Masking

None (Open label)

16 participants in 1 patient group

V-NAV users
Experimental group
Description:
Users who try the V-NAV for navigation tasks.
Treatment:
Other: V-NAV indoor navigation prototype

Trial contacts and locations

1

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Central trial contact

Philip R Schaefer, M.S.E; Elizabeth M Morgan

Data sourced from clinicaltrials.gov

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