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Non-invasive Training of the Inspiratory Muscles in Athletic Women

Pilot Study to Evaluate a Non-invasive Training System for Inspiratory Muscles in Athletic Women

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT07379060
Enrollment
21
Registered
2026-01-30
Start date
2025-09-15
Completion date
2026-06-01
Last updated
2026-02-03

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

Conditions

Respiratory Muscles

Brief summary

The goal of this clinical trial is to study whether there are significant differences between the control and experimental groups in terms of the improvement in lung function of the athletes who have performed Inspiratory muscle training with powerbreath. The main question it aims to answer is: • the study that power breath is effective in providing improvements in inspiratory muscle strength, lung function, exercise capacity, quality of life, analytical parameters, dyspnea, fatigue and activities of daily living and impacting their sporting success. Researchers will compare specific powerbreath training with nettraining period without this device. Participants will: * Perform regular sports training along with powerbreath training for 10 weeks * A washout period of two months * Perform regular sports training for 10 weeks

Interventions

DEVICEInspiratory Muscle Training 1

Inspiratory Muscle Training using the no invasive device. This training consists of 30 breaths, twice daily, with a resistance load set between 40% and 60% of their Maximum Inspiratory Pressure. The intervention will last for 10 weeks

DEVICEInspiratory Muscle Training 2

Inspiratory Muscle Training using the no invasive device. This training consists of 30 breaths, twice daily, with a resistance load set between 40% and 60% of their Maximum Inspiratory Pressure. The intervention will last for 10 weeks

Sponsors

University of Vigo
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
CROSSOVER
Primary purpose
TREATMENT
Masking
DOUBLE (Investigator, Outcomes Assessor)

Eligibility

Sex/Gender
FEMALE
Age
16 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Female athletes from the Galician Center for Sports Technification (CGTD) in the city of Pontevedra. * Sign the informed consent document. * Possession of the mental capacity required to participate in the study

Exclusion criteria

* Age below the legal healthcare age (16 years). * Lack of skills necessary to operate the no invasive device

Design outcomes

Primary

MeasureTime frameDescription
Power breath. Maximum Inspiratory PressureFrom enrollment to the end of treatment at 10 weeksThis training consists of 30 breaths, twice daily, with a resistance load set between 40% and 60% of their Maximum Inspiratory Pressure

Countries

Spain

Outcome results

None listed

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