Effect of a Respiratory Training Program on Woodwind and Brass Players

NCT ID: NCT06175286

Last Updated: 2024-02-05

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

COMPLETED

Clinical Phase

NA

Total Enrollment

20 participants

Study Classification

INTERVENTIONAL

Study Start Date

2023-04-01

Study Completion Date

2023-06-30

Brief Summary

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This project will study the effect of a respiratory training program on woodwind and brass players, using an inspiratory muscle training equipment. The goal is to understand whether it is possible to develop the inspiratory muscles of wind players through regular and planned training. Fourteen young wind players will be selected, in which 7 will be male and 7 will be female, playing different instruments. Inspiratory muscle training will be performed with the POWERBreath Plus Medium Resistance, and will consist of 30 maximal inspirations, twice a day, for 5 weeks.

Detailed Description

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This project will study the effect of a respiratory training program on woodwind and brass players, using an inspiratory muscle training equipment. The goal is to understand whether it is possible to develop the inspiratory muscles of wind players through regular and planned training. Fourteen young wind players will be selected, in which 7 will be male and 7 will be female, playing different instruments: transverse flute (1), oboe (2), saxophone (4), horn (4), trumpet (1), trombone (1) and tuba (1). Inspiratory muscle training will be performed with the POWERBreath Plus Medium Resistance, and will consist of 30 maximal inspirations, twice a day, for 5 weeks. The participants will be instructed on the use, handling and cleaning of the equipment. The participants will be instructed to use the equipment in a comfortable position, with a good posture, and will be instructed on how they should execute the inspiratory training: inhale to the maximum limit, with intensity, and exhale slowly and relaxed. An explanation will also be given about the calibration of the POWERbreathe, and the initial resistance level will be established based on the calculation of 50% of the Maximal Inspiratory Pressure of each participant, previously measured. Participants will also be instructed on how to increase the resistance level of POWERbreathe. The increase would be 1/4 of a level, whenever they no longer feel tired after a 30-inhalation workout. A questionnaire will be applied before, during and after the inspiratory training and they will be asked to record the daily use of the equipment in an online form, created for the purpose of recording its use by each participant. Assessment will be executed with the standard Borg Scale and the modified Borg scale. Surface electromyography (sEMG) of the right sternocleidomastoid, the right scalene muscles, the diaphragm and the right rectus abdominis will also be tested. Maximal inspiratory pressure and spirometry testing, specifically volume of forced vital capacity (FVC) or forced expiratory volume in one second (FEV1) and FEV1/FVC ratio will also be assessed.

Conditions

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Respiratory Function

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

CROSSOVER

Primary Study Purpose

OTHER

Blinding Strategy

NONE

Study Groups

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POWERBreath

Subjects will train with the POWERBreath twice per day, for 30 continous breaths

Group Type EXPERIMENTAL

POWERBreath Plus Medium Resistance training device

Intervention Type OTHER

30 inspirations with the POWERBreath Plus Medium Resistance training device, twice per day for 5 weeks

Control

Subjects will carry on with their normal daily life

Group Type NO_INTERVENTION

No interventions assigned to this group

Interventions

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POWERBreath Plus Medium Resistance training device

30 inspirations with the POWERBreath Plus Medium Resistance training device, twice per day for 5 weeks

Intervention Type OTHER

Eligibility Criteria

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Inclusion Criteria

* 18 years of age or over
* 10 years of musical experience

Exclusion Criteria

* lung disease
Minimum Eligible Age

18 Years

Maximum Eligible Age

65 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

Yes

Sponsors

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Aveiro University

OTHER

Sponsor Role lead

Responsible Party

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MARIO ALEXANDRE GONÇALVES LOPES

Adjunct Professor

Responsibility Role PRINCIPAL_INVESTIGATOR

Principal Investigators

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Catarina Monteiro

Role: PRINCIPAL_INVESTIGATOR

University of Aveiro

Locations

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Escola Superior de Saúde da Universidade de Aveiro

Aveiro, , Portugal

Site Status

Countries

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Portugal

References

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Drinkwater EJ, Klopper CJ. Quantifying the physical demands of a musical performance and their effects on performance quality. Med Probl Perform Art. 2010 Jun;25(2):66-71.

Reference Type BACKGROUND
PMID: 20795334 (View on PubMed)

Arend M, Kivastik J, Maestu J. Maximal inspiratory pressure is influenced by intensity of the warm-up protocol. Respir Physiol Neurobiol. 2016 Aug;230:11-5. doi: 10.1016/j.resp.2016.05.002. Epub 2016 May 12.

Reference Type RESULT
PMID: 27181328 (View on PubMed)

Other Identifiers

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Musician respiratory training

Identifier Type: -

Identifier Source: org_study_id

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