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Float First: An Index of Floating: Factors Affecting Floating in Different Populations

Float First: Categorising Factors Effecting Floating in Different Populations During Water Immersion.

Status
UNKNOWN
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT03982056
Enrollment
178
Registered
2019-06-11
Start date
2019-07-01
Completion date
2020-12-30
Last updated
2019-06-13

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

Conditions

Anthropometry, Floating Technique, Lung Function

Keywords

Floating, Sculling, water safety

Brief summary

The study involves measurements of body composition using a DEXA scanner, lung function, buoyancy and floating technique. An understanding of the effects of physiological and anthropometric measures on an individual's ability to float may lead to the creation of a 'Floatability Score' to aid current public information. With this floatability score a set of actions that people of certain body types should adopt in water will be created, to tailor the current public safety messaging in an attempt to ensure more people are aware of how they can float in water

Detailed description

Between 2000 and 2013 an average of 425 people in the UK drowned per annum, and a reported 100,000 people were involved in water-related emergencies involving search and rescue services. Approximately half had not intended to go into the water. Research identifies that in the first 1-3 minutes of immersion, during the cold shock response (CSR), there may be an increased probability of drowning fatalities. As a result of this, a theme of 'Float First' was created whereby individuals are advised to float for 1-3 minutes following immersion (by undertaking the minimum amount of activity possible to maximise the amount of air trapped in clothing layers and hence creating additional buoyancy) until the effects of the CSR have declined. However, a number of people have come forward indicating that despite the advice given, they are unable to float. This study is designed to establish the minimum activity level a person needs to stay afloat and combine this with anthropomorphic and physiological measures to develop advice for people of different shapes, sizes and body compositions.

Interventions

OTHERthis is an observational study there are no interventions

development of an index to provide appropriate information on a person's ability to float, based on Physiological and anthropometric characteristics

Sponsors

University of Portsmouth
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
Yes

Inclusion criteria

* All participants who feel confident in water which they can stand up in, aged 18 years and older (18-29 years for Phase 1). * The participant is willing and able to give informed consent for participation in the study. * Be able to climb up and down a set of steps to access the swimming flume

Exclusion criteria

* Have allergies to water or chlorinated water. * The participant is pregnant or suspects they may be pregnant. * Not able to climb up and down a set of steps to access the swimming flume

Design outcomes

Primary

MeasureTime frameDescription
Floating index2 minutesDescribes the actions required to stay afloat

Secondary

MeasureTime frameDescription
Masswith the two week study window - performed at the same time of day as the floating and DEXA scan measurementsMass of participant
Body compositionwith the two week study window - performed at the same time of day as the floating and DEXA scan measurementsa break down of the main components of the body (fat, lean tissue)
Standing Heightwith the two week study windowHeight of participant
Buoyancywith the two week study window - performed at the same time of day as the floating and DEXA scan measurementsthe buoyancy of the person floating in the water
Floating technique2 minutesThe technique required to float
Lung functionwith the two week study window - performed at the same time of day as the floating and DEXA scan measurementsthe volumes of the lungs namely, FVC, Tidal breathing, ERV and IRV

Countries

United Kingdom

Contacts

Primary ContactHeather Massey, PhD
heather.massey@port.ac.uk07891432744
Backup ContactAnt Shepherd, PhD
ant.shepherd@port.ac.uk

Outcome results

None listed

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