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

V-NAV: Advanced Indoor Navigation Aid for Individuals With Visual Impairments, End User Evaluation

Status
Suspended
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05647694
Enrollment
16
Registered
2022-12-12
Start date
2025-01-01
Completion date
2025-04-30
Last updated
2024-11-25

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Blindness and Low Vision

Keywords

blindness, indoor navigation

Brief summary

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.

Detailed 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.

Interventions

OTHERV-NAV indoor navigation prototype

Users will use the V-NAV prototype as an augmentation to their indoor navigation activities.

Sponsors

Vortant Technologies, LLC
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
OTHER
Masking
NONE

Masking description

The use of the app will not be masked.

Intervention model description

Participants will compare the value of the prototype app to their previous navigational experience without the app.

Eligibility

Sex/Gender
ALL
Age
12 Years to No maximum
Healthy volunteers
No

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.

Design outcomes

Primary

MeasureTime frameDescription
V-NAV effectiveness4 weeksA measurement of user impressions as to the value of the V-NAV navigation aid. Use of e.g., PIADS survey.

Secondary

MeasureTime frameDescription
V-NAV usability1 dayA measurement of how usable the V-NAV is. Use of e.g., NASA TLX survey.

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026