Inspiratory Muscle Endurance of Adults

March 2, 2023 updated by: Selda GOKCEN, Kutahya Health Sciences University

Determination of Respiratory Muscle Endurance in Healthy Adult Individuals

The aim of this study is to determine the reference value ranges for healthy adults of the incremental threshold load test, which evaluates respiratory muscle endurance.

Study Overview

Status

Completed

Conditions

Detailed Description

Since respiratory muscles are used in daily life at the submaximal level, evaluation of their endurance is more meaningful functionally. In addition, evaluation of endurance with respiratory muscle strength is effective in determining respiratory muscle dysfunction. Failure to routinely evaluate respiratory muscle endurance, which is one of the main components of respiratory muscle function, may lead to failure to identify respiratory muscle dysfunction in early stage respiratory patients who have not yet developed muscle strength loss. However, normal value ranges have not been determined for the respiratory muscle endurance test.

Determining the normal value ranges for this test will help determine muscle fatigue and investigate the physiological course in respiratory diseases.

Study Type

Observational

Enrollment (Actual)

112

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

      • Kutahya, Turkey, 43100
        • Kütahya Health Sciences 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

18 years to 35 years (Adult)

Accepts Healthy Volunteers

Yes

Genders Eligible for Study

All

Sampling Method

Probability Sample

Study Population

Healthy volunteers between the ages of 18-35

Description

Inclusion Criteria:

  • Being between the ages of 18-35
  • Not having any disease
  • Not exercising regularly
  • Not smoking

Exclusion Criteria:

  • Having a respiratory disease
  • Have heart disease
  • Have a neuromuscular disease
  • Have Scoliosis
  • Having had thoracic surgery
  • Having experienced the respiratory muscle endurance protocol before

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

  • Observational Models: Cohort
  • Time Perspectives: Cross-Sectional

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Incremental threshold loading test.
Time Frame: 15 minute
A measure of endurance of inspiratory muscles.
15 minute
Maximal inspiratory pressure
Time Frame: 20 minute
A measure of the strength of inspiratory muscles
20 minute

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Pulmonary function test - Forced expiratory volume in 1 second (FEV1)
Time Frame: 5 minute
The forced expiratory volume in 1 second (FEV1) is the volume of air (in liters) exhaled in the first second during forced exhalation after maximal inspiration. It is lung function test that are measured during spirometry. This pulmonary function test measurements were made to confirm that the respiratory function parameters of the participants were within the normal range. .
5 minute
Pulmonary function test - Forced vital capacity (FVC)
Time Frame: 5 minute
Forced vital capacity (FVC) is lung function test that are measured during spirometry. This pulmonary function test measurement is applied to confirm that the respiratory function parameters of the participants were within the normal range.
5 minute
Maximal voluntary ventilation (MVV)
Time Frame: 5 minute
It is a test that measures inspiratory endurance. MVV is the largest amount of air that a person can inhale and then exhale during a 12- to 15-s interval with maximal voluntary effort. It is determined by spirometry measurement.
5 minute
International Physical Activity Questionnaire - Short Form
Time Frame: 5 minute
This questionnaire assesses the types of intensity of physical activity and sitting time that people do as part of their daily lives are considered to estimate total physical activity in the metabolic equivalent of task (MET)-minute/week and time spent sitting.
5 minute

Other Outcome Measures

Outcome Measure
Measure Description
Time Frame
Anthropometric assessment
Time Frame: 5 minute
Body weight was assessed with a digital scale in the orthostatic position, without shoes, with minimal clothing. Height was measured with the feet parallel and adjacent to each other, the arms extended by the body, and the head in a neutral position. Correlations between inspiratory muscle endurance of the incremental threshold loading protocol and anthropometric characteristics will be shown.
5 minute

Collaborators and Investigators

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

Investigators

  • Principal Investigator: Selda Gokcen, Kütahya Health Sciences University
  • Study Director: Ozgen Aras, Kütahya Health Sciences University

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)

September 1, 2020

Primary Completion (Actual)

September 30, 2022

Study Completion (Actual)

January 18, 2023

Study Registration Dates

First Submitted

January 18, 2022

First Submitted That Met QC Criteria

February 2, 2022

First Posted (Actual)

February 14, 2022

Study Record Updates

Last Update Posted (Estimate)

March 3, 2023

Last Update Submitted That Met QC Criteria

March 2, 2023

Last Verified

March 1, 2023

More Information

Terms related to this study

Other Study ID Numbers

  • 100

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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