- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT07632950
Frequency-Dependent Effects of Mobilization-Based Exercise on Dynamic Postural Control in Orchestra Musicians: An Exploratory Randomized Controlled Trial
FREQUENCY-DEPENDENT EFFECTS OF MOBILIZATION-BASED EXERCISE ON DYNAMIC POSTURAL CONTROL IN ORCHESTRA MUSICIANS: AN EXPLORATORY RANDOMIZED CONTROLLED TRIAL
Study Overview
Status
Intervention / Treatment
Detailed Description
Posture is an important biomechanical concept that refers to the alignment of an individual's body segments against gravity in static or dynamic conditions. Postural control and balance are of great importance for individuals to perform daily living activities safely and effectively. Impairments in postural stability may lead to loss of balance, decreased movement efficiency, and mechanical loading on the musculoskeletal system, thereby predisposing individuals to problems such as pain and restricted movement. These negative outcomes become more pronounced particularly in groups whose professional performance largely depends on the precise and controlled use of the body.
Although there are various studies in the literature examining the effects of exercise programs aimed at preventing and correcting postural disorders, experimental studies investigating the effects of such interventions on postural control, particularly among orchestra musicians and in relation to different application frequencies, remain quite limited.
In this context, the present study aims to examine the effects of mobilization-based exercises and different application frequencies on postural control in individuals participating in an orchestra.
The study group consists of a total of 23 musicians who are flute and string instrument students enrolled in the orchestra-chamber music course. The participants were divided into three groups: a control group (n = 7), Experimental Group 1 (n = 8), and Experimental Group 2 (n = 8).
The research process will be carried out in four stages: pre-test, exercise intervention, acute test, and post-test. In the study, the Virtual Reality-Based Static Posturography System (StaticVR Virtualis) will be used to assess postural control.
It is hypothesized that the level of postural control will improve significantly over time in the experimental groups receiving mobilization-based exercises.
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
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Battalgazi
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Malatya, Battalgazi, Turkey (Türkiye), 0444
- Department of Physical Education and Sport Teaching, Faculty of Sports Sciences, Inonu University,, Malatya, Malatya 44280
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Adult
Accepts Healthy Volunteers
Description
Inclusion Criteria:
- Being an active musician participating in an orchestra.
- Being able to regularly attend all assessments and exercise sessions throughout the research process.
- Voluntarily agreeing to participate in the study.
- Having no neurological, orthopedic, or systemic health condition that could prevent posturography assessments or exercise applications.
Exclusion Criteria:
- Having a neurological disorder that could affect balance performance.
- Failing to regularly attend exercise sessions or assessment sessions.
- Having an acute musculoskeletal injury or serious orthopedic problem that could prevent assessment or exercise application.
- Wishing to withdraw from the study during the research process.
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Basic Science
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Experimental Group 1
For Experimental Group 1 (n = 8), the mobilization exercise program was applied once a week.
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The mobilization-based program, consisting of Cat-Camel Mobilization (2 × 15), Foam Roller Thoracic Extension (2 × 15), Scapular Retraction/Protraction (2 × 15), Pectoralis Minor Wall Stretch (2 × 30 s), Cervical Side Glide (2 × 15), and Shoulder Controlled Articular Rotations (2 × 12), was applied to Experimental Group 2 (n = 8) twice a week for 4 weeks.
|
|
Experimental: Experimental Group 2
For Experimental Group 2 (n = 8), the mobilization exercise program was applied twice a week.
|
The mobilization-based program, consisting of Cat-Camel Mobilization (2 × 15), Foam Roller Thoracic Extension (2 × 15), Scapular Retraction/Protraction (2 × 15), Pectoralis Minor Wall Stretch (2 × 30 s), Cervical Side Glide (2 × 15), and Shoulder Controlled Articular Rotations (2 × 12), was applied to Experimental Group 1 (n = 8) once a week for 4 weeks.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Change in postural control
Time Frame: Baseline (Week 0), acute assessment (Week 2), and post-intervention (Week 4)
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Postural control will be assessed using the StaticVR Virtualis virtual reality-based static posturography system.
Change in postural control will be determined by comparing measurements obtained at baseline, acute assessment, and post-intervention.
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Baseline (Week 0), acute assessment (Week 2), and post-intervention (Week 4)
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Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Acute change in postural control
Time Frame: Baseline (Week 0) and Week 2
|
Short-term change in postural control will be assessed using the StaticVR Virtualis system by comparing baseline and week 2 measurements.
|
Baseline (Week 0) and Week 2
|
|
Post-intervention change in postural control
Time Frame: Baseline (Week 0) and Week 4
|
Post-intervention change in postural control will be assessed using the StaticVR Virtualis system by comparing baseline and week 4 measurements.
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Baseline (Week 0) and Week 4
|
Collaborators and Investigators
Sponsor
Investigators
- Principal Investigator: Özgür EKEN, PhD, Assoc. Prof, İnönu University
Publications and helpful links
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
Keywords
Other Study ID Numbers
- INONU-POSTUR-2026-001
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
IPD Plan Description
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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