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Clinical Trials/NCT04366414
NCT04366414
Unknown
Not Applicable

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

Centro Universitario La Salle1 site in 1 country46 target enrollmentOctober 1, 2020

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Exercise Training
Sponsor
Centro Universitario La Salle
Enrollment
46
Locations
1
Primary Endpoint
Oxygen Saturation change
Last Updated
6 years ago

Overview

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.

Registry
clinicaltrials.gov
Start Date
October 1, 2020
End Date
December 14, 2020
Last Updated
6 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Sponsor
Centro Universitario La Salle
Responsible Party
Principal Investigator
Principal Investigator

Fran de Asís Fernández

Principal Investigator

Centro Universitario La Salle

Eligibility Criteria

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

Outcomes

Primary Outcomes

Oxygen Saturation change

Time Frame: Before 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 Outcomes

  • Heart Rate recovery(before and after training intervention (after 4 weeks))
  • Lung function (forced spirometry)(before and after training intervention (after 4 weeks))

Study Sites (1)

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