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Product Testing of the FaceView Mask™: Usability Survey

NCT04854694 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 202

Last updated 2025-04-10

Study results available
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Summary

The study aims to gather participants' perceptions of the novel transparent surgical N95 respirator vs. a conventional surgical N95 respirator. Following fitting of the masks, participants will complete a questionnaire to provide their perceptions of fit, comfort, ease of use, and benefit to communication.

Conditions

  • Hearing Disability

Interventions

DEVICE

FaceView Mask™

transparent surgical N95 respirator designed to improve communication

DEVICE

conventional surgical N95 respirator

standard N95 respirator

Sponsors & Collaborators

  • University of Arkansas

    lead OTHER

Principal Investigators

  • Samuel R Atcherson, PhD · University of Arkansas

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2022-11-15
Primary Completion
2024-02-29
Completion
2024-02-29
FDA Device
Yes

Countries

  • United States

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT04854694 on ClinicalTrials.gov