- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06823674
The Relationship of Core Endurance With Cervical Stabilization and Proprioception in Women With and Without Pilates Exercise
Study Overview
Status
Conditions
Intervention / Treatment
Study Type
Enrollment (Actual)
Contacts and Locations
Study Locations
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Mersin, Turkey, 33960
- Burak Sapmaz Fizyoterapi ve Danışmanlık Merkezi
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Adult
Accepts Healthy Volunteers
Sampling Method
Study Population
Description
Inclusion Criteria:
- Being between 20-50 years old
- Volunteering to participate in the study
- Having practiced Pilates at least 2 days a week for at least 12 weeks for the study group
- For the control group, not having participated in any pilates, yoga or exercise program in the last year and being sedentary according to the International Physical Activity Questionnaire
Exclusion Criteria:
- Presence of pain during assessments
- Cervical and/or lumbar disc herniation
- Spine pathology
Study Plan
How is the study designed?
Design Details
Cohorts and Interventions
Group / Cohort |
Intervention / Treatment |
|---|---|
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Women Who Don't Do Pilates
20 women aged 20-50 years who were sedentary according to the International Physical Activity Questionnaire and had not participated in any pilates or yoga exercise group in the last 1 year
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The study group was selected from women who did pilates exercises 2 days a week for at least 12 weeks under the supervision of a physiotherapist, while the control group was selected from women who did not participate in any pilates, yoga or exercise program in the last 1 year and were sedentary according to the International Physical Activity Questionnaire.
Lateral Bridge Test, Static Trunk Extension Test, Trunk Flexors Endurance Test, Cervical Joint Position Error Test, Cervical Region Deep Flexor Muscle Endurance Tests were applied to the participants and Craniocervical Flexion data of the participants were evaluated with Stabilizer Pressure Biofeedback Device.
The study group was selected from women who did pilates exercises 2 days a week for at least 12 weeks under the supervision of a physiotherapist, while the control group was selected from women who did not participate in any pilates, yoga or exercise program in the last 1 year and were sedentary according to the International Physical Activity Questionnaire.
Lateral Bridge Test, Static Trunk Extension Test, Trunk Flexors Endurance Test, Cervical Joint Position Error Test, Cervical Region Deep Flexor Muscle Endurance Tests were applied to the participants and Craniocervical Flexion data of the participants were evaluated with Stabilizer Pressure Biofeedback Device.
The study group was selected from women who did pilates exercises 2 days a week for at least 12 weeks under the supervision of a physiotherapist, while the control group was selected from women who did not participate in any pilates, yoga or exercise program in the last 1 year and were sedentary according to the International Physical Activity Questionnaire.
Lateral Bridge Test, Static Trunk Extension Test, Trunk Flexors Endurance Test, Cervical Joint Position Error Test, Cervical Region Deep Flexor Muscle Endurance Tests were applied to the participants and Craniocervical Flexion data of the participants were evaluated with Stabilizer Pressure Biofeedback Device.
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Women Doing Pilates
20 female volunteers between the ages of 20-50, practicing Pilates at least 2 days a week for at least 12 weeks
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The study group was selected from women who did pilates exercises 2 days a week for at least 12 weeks under the supervision of a physiotherapist, while the control group was selected from women who did not participate in any pilates, yoga or exercise program in the last 1 year and were sedentary according to the International Physical Activity Questionnaire.
Lateral Bridge Test, Static Trunk Extension Test, Trunk Flexors Endurance Test, Cervical Joint Position Error Test, Cervical Region Deep Flexor Muscle Endurance Tests were applied to the participants and Craniocervical Flexion data of the participants were evaluated with Stabilizer Pressure Biofeedback Device.
The study group was selected from women who did pilates exercises 2 days a week for at least 12 weeks under the supervision of a physiotherapist, while the control group was selected from women who did not participate in any pilates, yoga or exercise program in the last 1 year and were sedentary according to the International Physical Activity Questionnaire.
Lateral Bridge Test, Static Trunk Extension Test, Trunk Flexors Endurance Test, Cervical Joint Position Error Test, Cervical Region Deep Flexor Muscle Endurance Tests were applied to the participants and Craniocervical Flexion data of the participants were evaluated with Stabilizer Pressure Biofeedback Device.
The study group was selected from women who did pilates exercises 2 days a week for at least 12 weeks under the supervision of a physiotherapist, while the control group was selected from women who did not participate in any pilates, yoga or exercise program in the last 1 year and were sedentary according to the International Physical Activity Questionnaire.
Lateral Bridge Test, Static Trunk Extension Test, Trunk Flexors Endurance Test, Cervical Joint Position Error Test, Cervical Region Deep Flexor Muscle Endurance Tests were applied to the participants and Craniocervical Flexion data of the participants were evaluated with Stabilizer Pressure Biofeedback Device.
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
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Evaluation of Core Muscle Endurance between Pilates and Non-Pilates Groups Mann Whitney U Test Analysis
Time Frame: 01.05.2024- 20.07.2024
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The endurance of the core muscles was used to assess the static resistance of the core region with three tests evaluating the trunk flexors, trunk extensors and lateral bridge exercise.
Lateral Bridge Test, Static Trunk Extension Test (Sorensen Test) and Trunk Flexors Endurance Test were evaluated, measurements were recorded in seconds using a stopwatch.
The tests were repeated twice and the best result value was recorded.
The test was terminated when the person administered was unable to maintain the position or when the person said that they could not continue the test
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01.05.2024- 20.07.2024
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Mann Whitney U Test Analysis of Deep Neck Flexor Muscle Endurance Assessment Between Pilates and Non-Pilates Exercise Groups
Time Frame: 01.05.2024- 20.07.2024
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The participant was positioned in the supine hook position with hands relaxed on the abdomen.
The participant was instructed to pull his/her chin inwards (chin tuck) and lift his/her head off the bed while maintaining this position (approximately 2.5 cm).
The participant was asked to maintain this position for as long as possible without distortion and the time to maintain the position was recorded in seconds.
In order to perform the test correctly, the test was demonstrated to the individuals in a practical way before starting the test.
The test duration was kept short to prevent pain and fatigue of the participant.
The test was stopped when the jaw position (craniocervical flexion movement and jaw) was lost and sudden pain increased and the subject did not want to continue the test.
A single test was performed and the time was recorded in seconds.
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01.05.2024- 20.07.2024
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Chi-Square Test Analysis of Completion Distributions of Stages in Craniocervical Flexion Measurement with Stabilizer Pressure Biofeedback Device According to Groups
Time Frame: 01.05.2024- 20.07.2024
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In our study, after the participants were placed supine on the examination bed, the pressure cell was placed under the nape of the neck without inflation. The cell was inflated to 20 mmHg, taking care not to slide the cell to the lower cervical region. The participant was asked to press the chin towards the neck without lifting the head as if saying 'yes' (posterior cervical tilt). The participant was instructed to place the tongue on the upper palate, bring the lips together but keep the teeth slightly apart. The test consists of 5 stages. The value of the stabiliser device, which was set at 20 mmHg, was asked to increase by 2 mmHg at each stage until it reached 30 mmHg (20- 22- 24- 26- 28- 30 mmHg). The participant was asked to stay at each pressure value for 30 s and to complete the test by giving 30 s rest time after each pressure. The test was terminated at the stage where the participant could not complete the pressure value that he/she should keep constant for 30 s. |
01.05.2024- 20.07.2024
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Cervical Joint Position Error Test (Cervical Proprioception Assessment) Between Pilates and Non-Pilates Exercise Groups
Time Frame: 01.05.2024- 20.07.2024
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It is a measurement tool used to clinically assess participants' cervicocephalic proprioception ability.
Cervicocephalic proprioception describes the sense of position of one's head and neck in space.
It measures the ability of a blindfolded participant to accurately return the head position to a predetermined neutral point after cervical joint movement
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01.05.2024- 20.07.2024
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Collaborators and Investigators
Sponsor
Investigators
- Principal Investigator: Selin K Kalın, İstanbul Arel Üniversitesi
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Estimated)
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
- E-52857131-050.04-591162
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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