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The Effects of Inspiratory Muscle Training on Endurance Performance in Trained Athletes Under Normoxic and Hypoxic Conditions: A Gender-based Comprehensive Study (RespiPerf)

U

University of Lausanne (UNIL)

Status

Not yet enrolling

Conditions

Hypoxia, Altitude

Treatments

Procedure: Inspiratory Muscle Training (IMT)
Procedure: Normal Breathing

Study type

Interventional

Funder types

Other

Identifiers

NCT06121128
2023-01638

Details and patient eligibility

About

The POWERbreathe™ Plus: an Inspiratory Muscle Training device (IMT) with adjustable resistance.

Intervention lasts 4 weeks, with a frequency of 6 days/week, 2 series of 30 inspirations in the morning and evening.

Resistance based on 60% of the Pressure Maximal Inspiratory (PMI). Progressive increase in resistance every week.

Four laboratory visits: 2 pre-tests and 2 post-tests. Each pre- / post- test will go under normoxic and hypoxic conditions.

Measurements include Pulmonary functions (spirometry test); blood microcirculation (vascular occlusion test); gas exchanges (e.g. VO2max), cardiac parameters, heart rate variability, maximal aerobic power (incremental and time limit test)

Full description

The POWERbreathe™ Plus: an Inspiratory Muscle Training device (IMT) with adjustable resistance.

Intervention lasts 4 weeks, with a frequency of 6 days/week, 2 series of 30 inspirations in the morning and evening.

Resistance based on 60% of the Pressure Maximal Inspiratory (PMI). Progressive increase in resistance every week.

Four laboratory visits: 2 pre-tests and 2 post-tests. Each pre- / post- test will go under normoxic and hypoxic conditions.

Measurements include Pulmonary functions (spirometry test); blood microcirculation (vascular occlusion test); gas exchanges (e.g. VO2max), cardiac parameters, heart rate variability, maximal aerobic power (incremental and time limit test)

Enrollment

48 estimated patients

Sex

All

Ages

18 to 44 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • Inclusion: endurance trained athletes between 18 and 44 years old

Exclusion criteria

cardiovascular, metabolic and respiratory diseases, smoking history, prescription medication (Two medication families are known to interfere with FC:

  • Calcium channel blockers
  • Beta-blockers

Two families are known to interfere during spirometry measurements:

  • Inhaled beta-agonists
  • Inhaled glucocorticoids)

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

48 participants in 4 patient groups

Female Control Group (FCON)
Sham Comparator group
Description:
female endurance trained athletes between 18 and 44 years old
Treatment:
Procedure: Normal Breathing
Female Training Group (FTRAIN)
Experimental group
Description:
female endurance trained athletes between 18 and 44 years old
Treatment:
Procedure: Inspiratory Muscle Training (IMT)
Male Control Group (MCON)
Sham Comparator group
Description:
male endurance trained athletes between 18 and 44 years old
Treatment:
Procedure: Normal Breathing
Male Training Group (MTRAIN)
Experimental group
Description:
male endurance trained athletes between 18 and 44 years old
Treatment:
Procedure: Inspiratory Muscle Training (IMT)

Trial contacts and locations

0

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Data sourced from clinicaltrials.gov

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