Non-invasive Training of the Inspiratory Muscles in Athletic Women

N/AActive Not RecruitingNCT07379060

University of Vigo21 enrolled

Overview

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

Study Type

INTERVENTIONAL

Allocation

RANDOMIZED

Purpose

TREATMENT

Masking

DOUBLE

Enrollment

Conditions

Respiratory Muscles

Interventions

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

Inspiratory Muscle Training 2DEVICE

Eligibility

Sex: FEMALEMin age: 16 Years

Medical Language ↔ Plain English

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

Locations (1)

Faculty of Physiotherapy

Pontevedra, Pontevedra, Spain

Outcomes

Primary Outcomes

Power breath. Maximum Inspiratory Pressure

This training consists of 30 breaths, twice daily, with a resistance load set between 40% and 60% of their Maximum Inspiratory Pressure

Time frame: From enrollment to the end of treatment at 10 weeks

Data from ClinicalTrials.gov

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