The Effects of Core Stabilization Exercises on Respiratory Functions, Trunk Muscle Endurance and Postural Stabilization in Individuals Taking Basic Acting Education,
1 other identifier
interventional
31
1 country
1
Brief Summary
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
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P25-P50 for not_applicable
Started Jun 2020
Shorter than P25 for not_applicable
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
Study Start
First participant enrolled
June 1, 2020
CompletedPrimary Completion
Last participant's last visit for primary outcome
October 1, 2020
CompletedStudy Completion
Last participant's last visit for all outcomes
December 1, 2020
CompletedFirst Submitted
Initial submission to the registry
April 24, 2024
CompletedFirst Posted
Study publicly available on registry
October 3, 2024
CompletedOctober 3, 2024
October 1, 2024
4 months
April 24, 2024
October 2, 2024
Conditions
Keywords
Outcome Measures
Primary Outcomes (8)
Pulmonary Function Test. Forced vital capacity (FVC)
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)
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)
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)
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
through study completion, an average of 1 year
Trunk Muscles Endurance. Biering-Sorenson Test
through study completion, an average of 1 year
Trunk Muscles Endurance. Lateral Bridge Test
through study completion, an average of 1 year
Assessment of Postural Stabilization
Flamingo balance test
through study completion, an average of 1 year
Study Arms (2)
Control group
NO INTERVENTIONdiaphragm training exercises within the scope of basic acting education;The control group was evaluated at the beginning and at the end of the study.
exercise group
ACTIVE COMPARATORdiaphragm 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.
Interventions
Eligibility Criteria
You may qualify if:
- 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.
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
Yeditepe University
Istanbul, Turkey (Türkiye)
MeSH Terms
Interventions
Intervention Hierarchy (Ancestors)
Study Officials
- PRINCIPAL INVESTIGATOR
feyza Sule BADILLI HANTAL, PhD
Yeditepe University
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- NONE
- Purpose
- PREVENTION
- Intervention Model
- SINGLE GROUP
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Asst.Prof
Study Record Dates
First Submitted
April 24, 2024
First Posted
October 3, 2024
Study Start
June 1, 2020
Primary Completion
October 1, 2020
Study Completion
December 1, 2020
Last Updated
October 3, 2024
Record last verified: 2024-10
Data Sharing
- IPD Sharing
- Will share
- Shared Documents
- STUDY PROTOCOL
- Time Frame
- when trail number is registered and for 5 years
- Access Criteria
- study protocol will be shared when asked from the investigators
When the study is registered IPD can be shared with whom contacts with the investigators