Evaluation of Full Face Snorkel Masks (FFSMs)

Sponsor
Duke University (Other)
Overall Status
Completed
CT.gov ID
NCT04783688
Collaborator
Divers Alert Network (Other)
10
1
1
3.1
3.2

Study Details

Study Description

Brief Summary

Recently, multiple models of Full Face Snorkel Mask (FFSM) have entered the retail market. However, several fatalities have been reported to the non-profit agency Divers Alert Network (DAN) for snorkelers who were using FFSMs, and most of these fatality reports have unclear or unreported causes of death. This project is to determine the characteristics of the FFSMs when they are in use by snorkelers. Volunteers will be asked to snorkel in a water tank while breathing through several models of commercially available FFSM, one at at time.

Condition or Disease Intervention/Treatment Phase
  • Other: Full Face Snorkel Mask (FFSM)
N/A

Detailed Description

The scientific testing will take place in the water tank of Foxtrot chamber at the Duke Center for Hyperbaric Medicine & Environmental Physiology. This Center (referred to as "Duke Hyperbarics") has a long history of testing various aspects of undersea physiology and causes of injury and death. Duke Hyperbarics will conduct the physical tests, and DAN (Divers Alert Network) personnel will also supervise the scientific testing.

The experimental test subjects will be divided into two categories. Before testing, both categories will come in for a screening day, where they will go through the informed consent process and be medically screened for safety to perform activity. For the first category of subjects (Group A), five volunteer subjects will be recruited with no restrictions on age or fitness level. An effort will be made to include representative test subjects from older age ranges (>35 years old) in this group. To ensure they can safely perform light activity, they will be screened for cardiovascular disease, both by questionnaire and by a physical exam during the screening day.

The second group (Group B) will be age 18-40, non-smoking, and screened for fitness using a physical exam and a VO2max test. The reason for these two groups is to ensure that a spectrum of test subjects is examined across the comprehensive range of ages and fitness levels that may participate in snorkeling as recreation.

The testing will be designed to assess the function of the FFSMs produced by multiple brands compared to each other as well as compared to conventional snorkels. Test subjects will be positioned horizontally in warm water. They will be face-down on a bicycle ergometer, grasping handlebars for stability. On the test day, each subject will undergo three test procedures, using first a conventional snorkel then two different brands of FFSM while pedaling the underwater bicycle. Group A will be asked to pedal at a rate that is comfortable for them, while Group B will be given a targeted higher work rate to achieve.

For each FFSM test, the test subject will be asked to place the mask on themselves but provided no further instruction. The pressure exerted by the mask on the forehead will also be measured by placing a small, flexible, force-sensitive gauge between the skirt and the skin (this gauge needs to be in place for only a few seconds and will be removed before snorkeling). At the end of each test, the subjects will be asked to remove the FFSM quickly in response to an audible or visual alarm that will appear three times at randomized intervals. Their ability to remove the masks quickly will be timed.

Study Design

Study Type:
Interventional
Actual Enrollment :
10 participants
Allocation:
N/A
Intervention Model:
Single Group Assignment
Intervention Model Description:
Study is a measurement of subjects performing normal tasks in a controlled environment, with physiological measurementsStudy is a measurement of subjects performing normal tasks in a controlled environment, with physiological measurements
Masking:
None (Open Label)
Primary Purpose:
Basic Science
Official Title:
Evaluation of a Full Face Snorkel Mask (FFSM)
Actual Study Start Date :
Mar 9, 2021
Actual Primary Completion Date :
Jun 11, 2021
Actual Study Completion Date :
Jun 11, 2021

Arms and Interventions

Arm Intervention/Treatment
Experimental: Experimental Group

All subjects will snorkel using the same FFSMs.

Other: Full Face Snorkel Mask (FFSM)
A mask used for snorkeling that covers the entire face, as opposed to a conventional snorkel, which is held in the mouth only.

Outcome Measures

Primary Outcome Measures

  1. Fractional level of oxygen in the breathing gas (at steady state) provided by the different mask models [Estimated 4 hours long]

    The breathing gas provided to the snorkeler by the masks will be measured continuously throughout the experiment using a mass spectrometer.

  2. Fractional level of carbon dioxide in the breathing gas (at steady state) provided by the different mask models [Estimated 4 hours long]

    The breathing gas provided to the snorkeler by the masks will be measured continuously throughout the experiment using a mass spectrometer.

Secondary Outcome Measures

  1. Speed of removal of the different FFSM models [Estimated 20 minutes]

    The speed at which subjects can remove the different models of FFSM will be timed and measured in seconds for comparison between models.

Eligibility Criteria

Criteria

Ages Eligible for Study:
N/A and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
Yes
GROUP A:
Inclusion Criteria:
  • Preferred >35 years old

  • Safe to perform light activity

Exclusion Criteria:
  • Subjects must NOT be certified SCUBA divers
GROUP B:
Inclusion Criteria:
  • Age 18-40

  • VO2max exercise test results >30 mL/kg/min for female, >35 mL/kg/min for male

Exclusion Criteria:
  • Subjects must NOT be certified SCUBA divers

  • May not be active smokers

Contacts and Locations

Locations

Site City State Country Postal Code
1 Duke University Center for Hyperbaric Medicine & Environmental Physiology Durham North Carolina United States 27710

Sponsors and Collaborators

  • Duke University
  • Divers Alert Network

Investigators

  • Principal Investigator: Rachel Lance, PhD, Duke University Health System, Department of Anesthesiology

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Duke University
ClinicalTrials.gov Identifier:
NCT04783688
Other Study ID Numbers:
  • Pro00106241
First Posted:
Mar 5, 2021
Last Update Posted:
Jul 14, 2021
Last Verified:
Mar 1, 2021
Individual Participant Data (IPD) Sharing Statement:
No
Plan to Share IPD:
No
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No

Study Results

No Results Posted as of Jul 14, 2021