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Breathing Protocol in Breath-hold Divers

Breathing Protocol on Oxygen Saturation Recovery After a Dynamic Apnoea in Breath-hold Divers: a Single-blind, Randomized Clinical Trial

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04366414
Enrollment
46
Registered
2020-04-28
Start date
2020-10-01
Completion date
2020-12-14
Last updated
2020-04-28

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

Conditions

Apnea, Breathholding, Breathing Exercises, Exercise Training

Brief summary

The aim of this randomized controlled trial study was to assess the effects of an 4-week exercise program on the recovery capacity after a voluntary maximal apnea. Participants will be randomly allocated to perform an experimental breathing protocol (NR-HB), or an usual training using their usual breathing (UB) protocol.

Detailed description

It is a multi-center study. 2 different Spanish Freedivers Centres are included in the study (Madrid and Zaragoza). Divers were randomly assigned to receive an experimental training (NR-HB) or to be included in the Control Group (UB). The trial included two study visits. Each exercise training program will be applied sessions per week during 4 weeks. Participants received baseline assessments at the beginning of any intervention, and post-intervention assessments at the end of the fourth week.

Interventions

OTHERhook breathing removing nose-clip

Participants will perform 3 days per week of usual training, involving intense exercise 8 submaximes-dynamic apnoeas with 3-minute recovery between each one per session, and continuous training of free style swimming at moderate effort over 30 minutes, including warm-up, recovery between intervals and cool down. The experimental breathing protocol consisted on to remove nose-clip previous to surface and then perform hook breathing during 20 seconds.

OTHERusual breathing (UB)

Participants will perform 3 days per week of usual training, involving intense exercise 8 submaximes-dynamic apnoeas with 3-minute recovery between each one per session, and continuous training of free style swimming at moderate effort over 30 minutes, including warm-up, recovery between intervals and cool down.

Sponsors

Centro Universitario La Salle
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Outcomes Assessor)

Masking description

single-blind

Intervention model description

parallel-group

Eligibility

Sex/Gender
ALL
Age
18 Years to 60 Years
Healthy volunteers
Yes

Inclusion criteria

* Absence of pain or illness * No changes in cognitive ability * Over 18 years old. * Member of the Spanish Federation of Underwater Activities. * Positive medical examination that allows the diver to practice voluntary apnea.

Exclusion criteria

* People with systemic diseases, tumors, infections, pacemakers, history of epilepsy, hydrophobia, pregnancy women, pharmacological treatment. * To be participating in other physical activities during the experimental research

Design outcomes

Primary

MeasureTime frameDescription
Oxygen Saturation changeBefore and after training intervention (after 4 weeks)Oxygen Saturation recovery will be record by the experimenters every 5 seconds by a handheld pulse-oximeter during the 1 min recovery time after a maximal dynamic apnea. The outcome was the length of the time to return to 95% SpO2 during the 1 min recovery time after maximal dynamic apnoea

Secondary

MeasureTime frameDescription
Heart Rate recoverybefore and after training intervention (after 4 weeks)Heart Rate will be record by the experimenters every 5 seconds by a handheld pulse-oximeter during the 1 min recovery time after a maximal dynamic apnea. The outcome was the length of the time to stabilize heart rate during these 1 minute.
Lung function (forced spirometry)before and after training intervention (after 4 weeks)The Spirometry will be perform according to American Thoracic Society criteria and was measured in litres. The maneuver will be perform 3 times and recording the best one.

Countries

Spain

Contacts

Primary ContactFrancisco de Asís Fernández, PhD
frandeasis@lasallecampus.es(+34) 91 7401 980

Outcome results

None listed

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