- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT03699566
Assessment of Trunk Muscle Endurance, Respiratory Functions and Respiratory Muscle Strength in Healthy Individuals
October 5, 2018 updated by: Fuat YÜKSEL, Gazi University
The Relationship Between Trunk Muscle Endurance, Respiratory Functions and Respiratory Muscle Strength in Healthy Individuals
The diaphragm forms the upper segment of the core structure.
At the same time, the diaphragm muscle acts as the first muscle in the inspiratory function.
The aim of this study was to investigate the relationship between respiratory functions and trunk muscle endurance.
In this context, respiratory muscle strengths, respiratory functions and body muscle endurance of the cases were measured.
Study Overview
Status
Completed
Conditions
Intervention / Treatment
Detailed Description
The study was conducted on 60 healthy volunteers ranging in age from 20 to 36 years.
27 woman and 33 men participated in the study.
Respiratory muscle strength, trunk muscle endurance, pulmonary function test values and physical activity levels were evaluated for the subjects participating in the study.Respiratory muscle strength and respiratory function tests were performed with a Cosmed Pony Fx portable spirometer.
Trunk muscle endurance of the individuals were evaluated by prone bridge, side bridge, flexor endurance and sorensen test.
Study Type
Observational
Enrollment (Actual)
60
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
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Ankara, Turkey
- Gazi University
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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
16 years to 63 years (Adult, Older Adult)
Accepts Healthy Volunteers
N/A
Genders Eligible for Study
All
Sampling Method
Probability Sample
Study Population
Healthy volunteers
Description
Inclusion Criteria:
- Not having any chronic disease
- Not being pregnant
Exclusion Criteria:
- History of cardiopulmonary disease.
- Morbid obesity
- Major surgical history
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: Other
- Time Perspectives: Other
Cohorts and Interventions
Group / Cohort |
Intervention / Treatment |
---|---|
Healthy volunteers
Individuals aged 18-65 without chronic disease. Interventions: Assessment of Respiratory Muscle Strength, Spirometer, Trunk Muscles Endurance Tests |
The maximal voluntary inspiratory (PImax) and expiratory (PEmax) pressure measurements of the subjects were performed using Cosmed Pony FX model (Italy 2001) while the subjects were in the sitting position with a nose clip.
Spirometric measurements were conducted with Cosmed, Pony FX (descopt spirometer- Italy 2001) spirometer using a nose clips while the subjects were in 90 degree relaxed sitting position.
Trunk muscle endurance of the subjects was measured using four different tests (Side Bridge Test- SBT, Prone Bridge Test- PBT, Flexor Endurance Test- FET, Sorenson Test- ST).
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Maximal voluntary inspiratory (PImax)
Time Frame: Baseline assessment no follow- up
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inspiratory pressure measurement in cm H2O
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Baseline assessment no follow- up
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Prone Bridge Test
Time Frame: Baseline assessment no follow- up
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Trunk endurance test aganist the time
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Baseline assessment no follow- up
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Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Maximal voluntary expiratory (PEmax)
Time Frame: Baseline assessment no follow- up
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Expiratory pressure measurement in cm H2O
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Baseline assessment no follow- up
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Side Bride Test
Time Frame: Baseline assessment no follow- up
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Trunk endurance test aganist the time
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Baseline assessment no follow- up
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Forced Vital Capacity ( FVC)
Time Frame: Baseline assessment no follow- up
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Dinamic volume measure for lungs
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Baseline assessment no follow- up
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Forced Expiratuar Volume 1. Second ( Fev1)
Time Frame: Baseline assessment no follow- up
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Dinamic volume measure for lungs
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Baseline assessment no follow- up
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Abdominal Flexor Endurance Test
Time Frame: Baseline assessment no follow- up
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Trunk endurance test aganist the time
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Baseline assessment no follow- up
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Sorensen Test
Time Frame: Baseline assessment no follow- up
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Back Muscles endurance test aganist the time
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Baseline assessment no follow- up
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Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Collaborators
Investigators
- Study Chair: Nevin Güzel, prof. dr., Gazi 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)
March 10, 2017
Primary Completion (Actual)
June 15, 2017
Study Completion (Actual)
August 15, 2017
Study Registration Dates
First Submitted
October 5, 2018
First Submitted That Met QC Criteria
October 5, 2018
First Posted (Actual)
October 9, 2018
Study Record Updates
Last Update Posted (Actual)
October 9, 2018
Last Update Submitted That Met QC Criteria
October 5, 2018
Last Verified
October 1, 2018
More Information
Terms related to this study
Other Study ID Numbers
- Fuat1
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Undecided
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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