The Relationship of Core Endurance With Cervical Stabilization and Proprioception in Women With and Without Pilates Exercise

February 8, 2025 updated by: Selin Kalın, Istanbul Arel University
The aim of this study was to investigate the relationship between core endurance and cervical stabilization and proprioception in women with and without Pilates exercise. The study was conducted with 40 volunteer female participants aged 20-50 years. 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 Flexor 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 and the results were recorded. These results indicate that high performance in core endurance is associated with improved performance in cervical stabilization. As a result of this study, it was concluded that Pilates has a significant effect on core endurance, cervical stabilization and proprioception in women.

Study Overview

Study Type

Observational

Enrollment (Actual)

40

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

      • Mersin, Turkey, 33960
        • Burak Sapmaz Fizyoterapi ve Danışmanlık Merkezi

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

Sampling Method

Probability Sample

Study Population

Group of 20 participants doing pilates exercise 20 participants in the group without pilates exercise

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

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

Cohorts and Interventions

Group / Cohort
Intervention / Treatment
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
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.
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
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.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Evaluation of Core Muscle Endurance between Pilates and Non-Pilates Groups Mann Whitney U Test Analysis
Time Frame: 01.05.2024- 20.07.2024
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
01.05.2024- 20.07.2024
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
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.
01.05.2024- 20.07.2024
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

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
Cervical Joint Position Error Test (Cervical Proprioception Assessment) Between Pilates and Non-Pilates Exercise Groups
Time Frame: 01.05.2024- 20.07.2024
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
01.05.2024- 20.07.2024

Collaborators and Investigators

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

Investigators

  • Principal Investigator: Selin K Kalın, İstanbul Arel Üniversitesi

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)

May 1, 2024

Primary Completion (Actual)

July 20, 2024

Study Completion (Estimated)

March 1, 2025

Study Registration Dates

First Submitted

January 6, 2025

First Submitted That Met QC Criteria

February 8, 2025

First Posted (Actual)

March 25, 2025

Study Record Updates

Last Update Posted (Actual)

March 25, 2025

Last Update Submitted That Met QC Criteria

February 8, 2025

Last Verified

February 1, 2025

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)?

UNDECIDED

IPD Plan Description

Çalışma boyunca toplanan tüm IPDler paylaşılabilir.

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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