The Effect of Respiratory on Sports Performance in Archers

March 13, 2024 updated by: Halic University

The Effect of Pulmonary Functions and Respiratory Muscle Strength on Sports Performance in Elite Archers

Purpose: The physical, physiological, and functional characteristics of archers affect target shooting performance. In our study, we aimed to examine the effect of pulmonary functions and respiratory muscle strength on sports performance in archers.

Methods: Our study included 46 (27 female, 19 male) professional archers registered in archery sports clubs. Sociodemographic and physical characteristics were recorded. Pulmonary function test (PFT), respiratory muscle strength, shooting performance test, Moberg-pickup collection test, Nelson hand reaction test, and Fatigue Severity Scale (FSS) were applied to all participants.

Study Overview

Status

Completed

Study Type

Interventional

Enrollment (Actual)

46

Phase

  • Not Applicable

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

      • Istanbul, Turkey
        • Halic University

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

  • Adult

Accepts Healthy Volunteers

Yes

Description

Inclusion Criteria:

  • Between 18-30 years old,
  • Professional archers.

Exclusion Criteria:

  • Participants who had COVID-19 (Coronavirus Disease) in the last 2 months,
  • Musculoskeletal disorders,
  • Orthopedic surgery,
  • Smoking history,
  • Neurologic and pulmonary diseases.

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Primary Purpose: Other
  • Allocation: N/A
  • Interventional Model: Single Group Assignment
  • Masking: None (Open Label)

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Other: Results of sports performance parameters values in archers
Sociodemographic and physical characteristics, Pulmonary function test (PFT), respiratory muscle strength, shooting performance test, Moberg-pickup collection test, Nelson hand reaction test, and Fatigue Severity Scale (FSS)
Evaluation of respiratory functions, respiratory muscle strength and shooting performance in archers
Other Names:
  • performance evaluation

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
FEV1 (liter)
Time Frame: at the enrollment
This is the amount of air with pulmonary function test that the patient can force out of their lungs in one second.
at the enrollment
FEV1 (%-percentage)
Time Frame: at the enrollment
This is the percentage of air with pulmonary function test that the patient can force out of their lungs in one second.
at the enrollment
FVC (liter)
Time Frame: at the enrollment
This is the greatest total amount of air patient can forcefully breathe out after breathing in as deeply as possible.
at the enrollment
FEV1/FVC (percentage)
Time Frame: at the enrollment
The FEV1/FVC ratio is a number that represents the percentage of patient lung capacity patient is able to exhale in one second.
at the enrollment
Inspiratory muscle test
Time Frame: at the enrollment
Maximal inspiratory pressure (MIP) is going to measured using a mouth pressure meter (MicroRPM; MicroMedical, UK) according to the guideline of ATS and European Respiratory Society (ERS).
at the enrollment
Expiratory muscle test
Time Frame: at the enrollment
Maximal expiratory pressure (MEP) is going to measured using a mouth pressure meter (MicroRPM; MicroMedical, UK) according to the guideline of ATS and European Respiratory Society (ERS).
at the enrollment
FVC (%-percentage)
Time Frame: 7 months
This is the percentage of air patient can forcefully breathe out after breathing in as deeply as possible.
7 months
Shooting performance
Time Frame: at the enrollment
The high shooting score indicates high arrow shooting performance.
at the enrollment
Nelson Hand Reaction Test
Time Frame: at the enrollment
The average value when the participants catch the ruler for three attempts
at the enrollment
Moberg-pickup collection test
Time Frame: at the enrollment
Assess manual dexterity and function by measuring the time it takes to pick up twelve different small objects (screws, paper clips, rings, safety pins, small nuts, coins, and wrenches)
at the enrollment
The Fatigue Severity Scale (FSS)
Time Frame: at the enrollment
Assess fatigue severity with 9-item self reporting scale
at the enrollment

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

July 26, 2021

Primary Completion (Actual)

January 1, 2022

Study Completion (Actual)

January 1, 2022

Study Registration Dates

First Submitted

February 15, 2024

First Submitted That Met QC Criteria

March 13, 2024

First Posted (Actual)

March 20, 2024

Study Record Updates

Last Update Posted (Actual)

March 20, 2024

Last Update Submitted That Met QC Criteria

March 13, 2024

Last Verified

March 1, 2024

More Information

Terms related to this study

Other Study ID Numbers

  • zselcuk1

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

NO

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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