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"Living Low - Training High" Methods and Physiological Responses in Well-trained Swimmers

F

Faculdade de Motricidade Humana

Status

Not yet enrolling

Conditions

Normobaric Hypoxia
Normoxia
Hypoventilation

Treatments

Other: Repeated sprint

Study type

Interventional

Funder types

Other

Identifiers

NCT06253039
RSH swimmers

Details and patient eligibility

About

To overcome the lack of knowledge regarding the impact of different "living low, training high" methods on swimming performance, a 4-week intervention will be carried out to determine and compare the effects of three Repeated Sprints in Hypoxia (RSH) methods with each other and with a control group. Our goal is to characterize and compare the adaptations in swimming performance and in cardiorespiratory, metabolic, and muscle oxygenation responses that can arise after a 4-week training period of RSH and RSH-voluntary hypoventilation (VHL) performed in a ski-ergometer.

Full description

Recently, several new "living low training high" (LLTH) methods involving repeated sprints in hypoxia have shown promising results, especially in team sports. However, the underlying mechanisms remain mostly unclear, as does its effectiveness in improving swimming performance.

Hypoxemia can be induced by exposure to ambient hypoxia conditions, by voluntary hypoventilation at low lung volume, or by vascular occlusion (namely, blood flow restriction). Swimming performance is influenced by aerobic and anaerobic metabolism and could benefit from these different LLTH methods.

This project aims to compare the effects of repeated sprint training performed with a ski-ergometer 1) in a hypoxic chamber and 2) with voluntary hypoventilation on the performance of swimmers, as well as to characterize cardiorespiratory, metabolic, and muscle oxygenation adaptations that may contribute to the improvements achieved after four weeks of each of these types of training.

All groups will be evaluated before and after the supervised training period in three testing sessions in normoxia, separated by at least 24 hours within 7 days. Swimmers will perform: 1) time-trial (100 m front crawl) in the swimming pool to determine performance, V̇̇O2 peak, and lactate concentration following the test; 2) incremental test to exhaustion in the swim-ergometer to determine aerobic peak power, cardiorespiratory responses (V̇̇O2max, ventilatory thresholds), and maximal tissue deoxygenation; 3) time-trial test in the ski-ergometer (100 m) to access performance, muscle and pulmonary oxygen uptake kinetics, and the relative contribution of energetic systems.

Training sessions will be performed in the ski-ergometer and consist of 4 sets of 5x6s all-out sprints with 24s and 5 min of passive rest between the sprints and sets, respectively. In all testing and training sessions, pulse oxygen saturation will be measured for safety purposes.

Enrollment

36 estimated patients

Sex

All

Ages

18 to 30 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • Swimmers from both sexes;
  • With regular participation in National Championships;
  • More than five years of training experience;
  • No recent exposure/acclimatization to altitude;
  • No recent exposition to Blood Flow Restriction training.

Exclusion criteria

  • athletes who had an acclimatization experience or exposure to altitude lasting more than 10 days in the last 6 months;
  • pregnant or postpartum women;

Trial design

Primary purpose

Other

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

36 participants in 3 patient groups

Normobaric hypoxia (RSH)
Experimental group
Description:
The RSH group will perform training sessions in a normobaric hypoxic chamber at a simulated altitude of 3000 meters (FiO2 14.5%)
Treatment:
Other: Repeated sprint
Hypoventilation (RSH-VHL)
Experimental group
Description:
RSH-VHL group will be asked to exhale down to functional residual capacity just before each repetition and then hold their breath until the end of the sprint
Treatment:
Other: Repeated sprint
Normoxia (RSN)
Active Comparator group
Description:
The control group will perform the training sessions in normoxia (FIO2, 20.9%)
Treatment:
Other: Repeated sprint

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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