Influence of Different Methods of Respiratory Muscle Training on Athletic Performance and Pulmonary Function in Short-track Speedskaters

NCT ID: NCT05936723

Last Updated: 2023-07-10

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

UNKNOWN

Clinical Phase

NA

Total Enrollment

16 participants

Study Classification

INTERVENTIONAL

Study Start Date

2023-06-15

Study Completion Date

2023-07-30

Brief Summary

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This research aims to explore the impact of two distinct methods of respiratory muscle training, voluntary isocapnic hyperpnoea (VIH) and inspiratory pressure threshold loading (IPTL), on athletic performance and pulmonary function in short-track speedkaters. The study will employ a parallel group-randomized trial design and will span a period of six weeks, during which participants will undergo regular, partially supervised training sessions.

The primary objective of the research is to assess the changes in athletic performance resulting from respiratory muscle training using VIH and IPTL techniques. Athletic performance will be measured through a range of standardized performance tests relevant to the participants' specific sporting activities (Wingate Test, CPET, on-ice time-trial performance). Pulmonary function will be measured by spirometry examination.

The group will consist of healthy, highly-trained professional short-track speedskaters.

Detailed Description

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This study aims to investigate the effects of two different respiratory muscle training methods, namely voluntary isocapnic hyperpnoea (VIH) and inspiratory pressure threshold loading (IPTL), on athletic performance and pulmonary function. The research will adopt a parallel group-randomized trial design, spanning a six-week period of regular, partially supervised training sessions.

The primary objective is to evaluate changes in athletic performance resulting from respiratory muscle training using VIH and IPTL techniques. Standardized performance tests relevant to the participants' specific sports will be utilized (Wingate Test, CPET, on-ice time-trial performance).

In addition, the impact of respiratory muscle training on pulmonary function will be assessed, focusing on parameters such as forced vital capacity (FVC), forced expiratory volume in one second (FEV1), peak expiratory flow (PEF). These measurements will provide insights into the potential enhancements of respiratory muscle strength and function through VIH and IPTL.

Participants will be randomly assigned to either the VIH or IPTL training group. Regular training sessions will be conducted under partial supervision to ensure proper technique and adherence. Close monitoring will be implemented to track progress and identify any potential adverse effects.

The findings of this research will hold implications for athletes and individuals seeking to optimize their athletic performance and respiratory muscle function. By comparing the effects of VIH and IPTL, the study aims to identify the most effective respiratory muscle training method.

Ultimately, this research will contribute to the existing knowledge on respiratory muscle training and its potential benefits for athletes and individuals engaged in physical activities. The results obtained will provide evidence-based guidance for the development of targeted training protocols that can enhance athletic performance and respiratory health.

Conditions

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Respiratory Muscle Training

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

parallel group-randomized trial
Primary Study Purpose

OTHER

Blinding Strategy

NONE

Study Groups

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Voluntary Isocapnic Hyperpnoea (VIH)

Group performing respiratory muscle training with Voluntary Isocapnic Hyperpnoea (VIH) method.

Group Type ACTIVE_COMPARATOR

Respiratory Muscle Training - VIH

Intervention Type BEHAVIORAL

The VIH group will train every second day with gradual progression based on session length and breathing frequency. Participants will begin with 3 minutes of exercise with a frequency of 20 breaths·min-1 during the first session and add no more than 1 minute or 2 breaths·min-1 with each consecutive session.

Inspiratory Pressure Threshold Loading (IPTL)

Group performing respiratory muscle training with Inspiratory Pressure Threshold Loading (IPTL) method.

Group Type ACTIVE_COMPARATOR

Respiratory Muscle Training - ITPL

Intervention Type BEHAVIORAL

The IPTL group will train 5 days a week, twice a day, with at least 6 hours break between sessions. The session will consist of 30 dynamic inspiratory maneuvers with progressive overload based on gradually increased resistance. The VIH group will train every second day with gradual progression based on session length and breathing frequency. Participants will begin with 3 minutes of exercise with a frequency of 20 breaths·min-1 during the first session and add no more than 1 minute or 2 breaths·min-1 with each consecutive session.

Interventions

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Respiratory Muscle Training - VIH

The VIH group will train every second day with gradual progression based on session length and breathing frequency. Participants will begin with 3 minutes of exercise with a frequency of 20 breaths·min-1 during the first session and add no more than 1 minute or 2 breaths·min-1 with each consecutive session.

Intervention Type BEHAVIORAL

Respiratory Muscle Training - ITPL

The IPTL group will train 5 days a week, twice a day, with at least 6 hours break between sessions. The session will consist of 30 dynamic inspiratory maneuvers with progressive overload based on gradually increased resistance. The VIH group will train every second day with gradual progression based on session length and breathing frequency. Participants will begin with 3 minutes of exercise with a frequency of 20 breaths·min-1 during the first session and add no more than 1 minute or 2 breaths·min-1 with each consecutive session.

Intervention Type BEHAVIORAL

Eligibility Criteria

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Inclusion Criteria

* valid medical certificate to compete sports professionally,
* lack of ongoing medication intake,
* lack of any medical condition,
* lack of previous experience with RMT,
* performance caliber corresponding to at Elite/World Class (Participant Classification Framework, McKay 2022).

Exclusion Criteria

* any ongoing medication intake or medical condition.
Minimum Eligible Age

18 Years

Maximum Eligible Age

30 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Institute of Sport - National Research Institute, Poland

OTHER

Sponsor Role lead

Responsible Party

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Tomasz Kowalski

Principal Investigator

Responsibility Role PRINCIPAL_INVESTIGATOR

Locations

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Institute of Sport - National Research Institute

Warsaw, , Poland

Site Status

Countries

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Poland

Other Identifiers

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TK01/2023

Identifier Type: -

Identifier Source: org_study_id

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