- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT04477915
Effects of Two Different Exercise Practices on Maximum Oxygen Uptake and Pulmonary Function
The Effects of Auxiliary Respiratory Muscles Exercises and Core Stabilization Exercises on Maximum Oxygen Uptake and Pulmonary Function
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
The study will be carried out on volunteers after the approval of the ethics committee. Before the research, individuals and / or their relatives will be informed about the purpose and content of the study. Volunteer individuals between the ages of 18-25 without any known health problems will be included in the study after obtaining their informed consent.
Participants will be randomly divided into three groups: control group, core stabilization exercises and auxiliary respiratory muscles exercises.
In the core stabilization exercises and auxiliary respiratory muscles exercises groups, exercises will be carried out under the supervision of a physiotherapist 3 days in a week separate time periods. Core stabilization exercise include, plank, lateral plank, swimmer, flutter kick and bridge exercises. Auxiliary respiratory exercises include, strengthening and stretching exercises for trapezius, sternocleidomastoideus, pectoralis major and serratus anterior muscles. Our study will take 6 weeks. The demographic information of the participants will be recorded and the VO2max values of the participants before and after the study will be measured with the H / P Cosmos Mercury Med device using the balke protocol. Respiratory function tests of participants will be measured with Cosmed Fitmate Med device before and after the study.
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
-
-
-
Konya, Turkey, 42020
- KTO Karatay University
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Description
Inclusion Criteria:
- Healthy individuals without any known health problems
Exclusion Criteria:
- Acute myocardial infarction, Unstable angina, Uncontrolled cardiac arrhythmias, Endocarditis, Various symptomatic aortic stenosis, Acute pulmonary embolism, pulmonary infarction and deep vein thrombosis, Acute myocarditis, pericarditis, physically not enough fit to test safely
Study Plan
How is the study designed?
Design Details
- Primary Purpose: OTHER
- Allocation: RANDOMIZED
- Interventional Model: PARALLEL
- Masking: TRIPLE
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
---|---|
EXPERIMENTAL: Core stabilization Exercise
Core stabilization exercise include, plank, lateral plank, swimmer, flutter kick and bridge exercises.
Exercises will be carried out under the supervision of a physiotherapist 3 days in a week separate time periods.
Our study will take 6 weeks.
|
Core stabilization exercise include, plank, lateral plank, swimmer, flutter kick and bridge exercises.
|
EXPERIMENTAL: Auxiliary respiratory exercises
Auxiliary respiratory exercises include, strengthening and stretching exercises for trapezius, sternocleidomastoideus, pectoralis major and serratus anterior muscles.
exercises will be carried out under the supervision of a physiotherapist 3 days in a week separate time periods.
Our study will take 6 weeks.
|
Auxiliary respiratory exercises include, strengthening and stretching exercises for trapezius, sternocleidomastoideus, pectoralis major and serratus anterior muscles.
|
NO_INTERVENTION: Control
Control Group
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Change from baseline in Maximum oxygen uptake at 6 weeks
Time Frame: Baseline and week 6
|
the VO2max values of the participants before and after the study will be measured with the H / P Cosmos Mercury Med device using the Balke Ware protocol.
|
Baseline and week 6
|
Change from baseline in Pulmonary function tests at 6 weeks
Time Frame: Baseline and week 6
|
Forced expiratory volume in 1 second / forced vital capacity (FEV1/FVC), vital capacity and maximum voluntary ventilation (MVV) values of the participants will be measured with Cosmed Fitmate Med device before and after the study.
|
Baseline and week 6
|
Collaborators and Investigators
Sponsor
Study record dates
Study Major Dates
Study Start (ACTUAL)
Primary Completion (ACTUAL)
Study Completion (ACTUAL)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (ACTUAL)
Study Record Updates
Last Update Posted (ACTUAL)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Other Study ID Numbers
- KaratayUH
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
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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