The Effects of Core Stabilization Exercises on Respiratory Functions, Trunk Muscle Endurance and Postural Stabilization in Individuals Taking Basic Acting Education,

October 2, 2024 updated by: Feyza Sule BADILLI HANTAL, Yeditepe University

The aim of the study is to investigate the effects of a 8-week, core stabilization exercise program on respiratory functions, muscle trunk endurance and postural stabilization in individuals taking basic acting education. The main question it aims to answer is:

the effects of a 8-week, core stabilization exercise program on respiratory functions, muscle trunk endurance and postural stabilization in individuals taking basic acting education

Study Overview

Status

Completed

Conditions

Intervention / Treatment

Detailed Description

The aim of the study is to investigate the effects of a 8-week, core stabilization exercise program on respiratory functions, muscle trunk endurance and postural stabilization in individuals taking basic acting education. The respiratory functions were assessed by the spirometer. Trunk muscle endurance was assessed by Fleksor Trunk Endurance Test (FTET), Biering Sorenson Test (BST) and Lateral Bridge Test (LBT). Postural stabilization was evaluated by Flamingo Balance Test (FBT) and Y Balance Test (YBT). The participants were randomly divided into two groups as Exercise Group (EG) and Control Group (CG) . Both people in EG and CG were taken diaphragmatic training program according to BAE. The core stabilization exercise program was administered for EG, twice a week, 45 minutes a day and for a 8-week duration.

Study Type

Interventional

Enrollment (Actual)

31

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

  • Turkey
      • Istanbul, Turkey
        • Yeditepe 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

The inclusion criterias of this study are;

  • Being volunteer
  • whose ages between 18-40 years
  • whose taking basic acting education course at DC Kozmos Art Academy

Volunteers were excluded from the study if the following conditions will be presented:

  • chronic respiratory disease,
  • back pain within the last two months,
  • pregnancy,
  • refusal to sign the informed consent document.

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: Prevention
  • Allocation: Randomized
  • Interventional Model: Single Group Assignment
  • Masking: None (Open Label)

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
No Intervention: Control group
diaphragm training exercises within the scope of basic acting education;The control group was evaluated at the beginning and at the end of the study.
Active Comparator: exercise group
diaphragm training exercises within the scope of basic acting education and Planned exercises started to be implemented after one session of training. Exercise group was given exercises by the physiotherapist for 8 weeks, two days a week, during 45 minutes before the acting lessons started.
Other: exercise
core stabilization exercises

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Pulmonary Function Test. Forced vital capacity (FVC)
Time Frame: through study completion, an average of 1 year
Pulmonary Function Test assessed with spirometer Contec™ SP10W Hand-Held Spirometer according to American Thoracic Society (ATS) and European Respiratory Society (ERS) criteria.It was carried out properly . Forced vital capacity (FVC)
through study completion, an average of 1 year
Pulmonary Function Test. Forced expiratory volume at 1st second (FEV1)
Time Frame: through study completion, an average of 1 year
Pulmonary Function Test assessed with spirometer Contec™ SP10W Hand-Held Spirometer according to American Thoracic Society (ATS) and European Respiratory Society (ERS) criteria.It was carried out properly . Forced expiratory volume at 1st second (FEV1)
through study completion, an average of 1 year
Pulmonary Function Test. ratio (FEV1 / FVC)
Time Frame: through study completion, an average of 1 year
Pulmonary Function Test assessed with spirometer Contec™ SP10W Hand-Held Spirometer according to American Thoracic Society (ATS) and European Respiratory Society (ERS) criteria.It was carried out properly . Tiffeneau ratio (FEV1 / FVC)
through study completion, an average of 1 year
Pulmonary Function Test. Peak expiratory flow rate (PEF)
Time Frame: through study completion, an average of 1 year
Pulmonary Function Test assessed with spirometer Contec™ SP10W Hand-Held Spirometer according to American Thoracic Society (ATS) and European Respiratory Society (ERS) criteria.It was carried out properly . Peak expiratory flow rate (PEF) values
through study completion, an average of 1 year
Trunk Muscles Endurance. Trunk Flexors Endurance Test
Time Frame: through study completion, an average of 1 year
through study completion, an average of 1 year
Trunk Muscles Endurance. Biering-Sorenson Test
Time Frame: through study completion, an average of 1 year
through study completion, an average of 1 year
Trunk Muscles Endurance. Lateral Bridge Test
Time Frame: through study completion, an average of 1 year
through study completion, an average of 1 year
Assessment of Postural Stabilization
Time Frame: through study completion, an average of 1 year
Flamingo balance test
through study completion, an average of 1 year

Collaborators and Investigators

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

Sponsor

Yeditepe University

Investigators

  • Principal Investigator: feyza Sule BADILLI HANTAL, PhD, Yeditepe 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)

June 1, 2020

Primary Completion (Actual)

October 1, 2020

Study Completion (Actual)

December 1, 2020

Study Registration Dates

First Submitted

April 24, 2024

First Submitted That Met QC Criteria

October 2, 2024

First Posted (Actual)

October 3, 2024

Study Record Updates

Last Update Posted (Actual)

October 3, 2024

Last Update Submitted That Met QC Criteria

October 2, 2024

Last Verified

October 1, 2024

More Information

Terms related to this study

Keywords

Other Study ID Numbers

  • Yeditepe UniversityU

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

YES

IPD Plan Description

When the study is registered IPD can be shared with whom contacts with the investigators

IPD Sharing Time Frame

when trail number is registered and for 5 years

IPD Sharing Access Criteria

study protocol will be shared when asked from the investigators

IPD Sharing Supporting Information Type

  • STUDY_PROTOCOL

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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