- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT04834141
Correlation Between Thoracic Kyphosis Posture and Static Balance
Study Overview
Status
Intervention / Treatment
Detailed Description
Background:
Kyphosis is roughly a slight forward curvature of the spine. A slight kyphosis or posterior curvature is normal throughout the human body and is present in every individual. Hyperkyphotic is a kyphotic angle greater than 40° commonly measured on a lateral X-ray measured by the Cobb method between C7 and T12. Postural stability or balance is the ability to keep the center of mass within the boundaries of the support base. Moving the center of mass beyond the boundaries of the support base may cause postural instability and loss of balance. There are studies showing that kyphotic posture affects the center of gravity and affects fall in the elderly, but there are limited studies on the effect of balance in young individuals.
The Aim of This Study Is:
To study the correlation between the balance and severity of thoracic kyphosis will be investigated
Study Type
Enrollment (Actual)
Contacts and Locations
Study Locations
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Istanbul, Turkey, 34854
- Marmara University
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Sampling Method
Study Population
Fourty-six subjects who joined the study were healthy without any disease might affect balance, body posture, and denied a past history of vestibular disorders, syncope, seizures, or neurological disorders such as stroke or Parkinson's disease.
The study take place in Marmara university, Başıbüyük campus, between the period September 2020 to December 2020. Participants were recruited through online poster announcement, they directly contacted the primary investigator for booking an appointment. An appointment were made for the participants in the Faculty of Health Sciences, Physiotherapy and Rehabilitation Department, Biomechanics and Performance Analysis Laboratory, Marmara University.
Description
Inclusion Criteria:
- Adults aged 18 and over willing to attend the study.
- For those who join the thoracic kyphosis group, individuals with a kyphosis angle ≥ 40 degrees.
- Individuals with a kyphosis angle < 40 degrees for the control group.
Exclusion Criteria:
- Spine trauma, surgery, bone pathology, arthritis etc. have a history of illness Kyphotic deformity types are rounded back, Scheuermann's disease, hunched back, flat back and Dowager hump.
- Any spinal deformity, bone abnormality, postural deformity and disc herniation with / without peripheral symptoms.
- Body mass index (BMI), which is an indicator of obesity, is more than > 30.
- Complaining of balance problems, coordination problems, other neurological or vestibular diseases that affect body balance and posture.
- Having any orthopedic or neurological disease that affects the body joints or the integrity of the musculoskeletal system.
- Use of any medication that can cause dizziness or drowsiness in the last months.
Study Plan
How is the study designed?
Design Details
Cohorts and Interventions
Group / Cohort |
Intervention / Treatment |
|---|---|
|
Kyphotic Group
Participants with kyphosis angle ≥ 40 degrees joined the kyphosis group. FlexiCurve ruler method was used, which is a reliable tool for measuring kyphosis height and kyphosis index. In addition, it is non-invasive, inexpensive, and easy to use in a clinical setting. Static balance Assessment: Objective evaluation of the static balance evaluated by the NeuroCom Balance Manager System ® static posturography device (45 × 45 cm NeuroCom® System Version 8.1 Balance Manager International, Clackamas, Oregon, USA) |
The determination that the effect of thoracic kyphosis posture on trunk biomechanical alignment may be related to balance may contribute to new treatment recommendations in this area.
The aim of this study is to investigate whether the thoracic kyphosis posture has an effect on static balance.
Other Names:
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Control Group
Participants with kyphosis angle < 40 degrees for the control group. FlexiCurve ruler method was used, which is a reliable tool for measuring kyphosis height and kyphosis index. In addition, it is non-invasive, inexpensive, and easy to use in a clinical setting. Static balance Assessment: Objective evaluation of the static balance evaluated by the NeuroCom Balance Manager System ® static posturography device (45 × 45 cm NeuroCom® System Version 8.1 Balance Manager International, Clackamas, Oregon, USA) |
The determination that the effect of thoracic kyphosis posture on trunk biomechanical alignment may be related to balance may contribute to new treatment recommendations in this area.
The aim of this study is to investigate whether the thoracic kyphosis posture has an effect on static balance.
Other Names:
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
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Kyphosis Angle
Time Frame: 2 Months
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Kyphosis angle will be measured by felxicurve ruler, normally kyphosis angle below 40 degrees recognized as normal.
For participants with kyphosis angle above 40 degrees recognized as hyperkyphotic posture.
FlexiCurve ruler method is valid and reliable to the gold standard.
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2 Months
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Static Balance Measures
Time Frame: 2 Months
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NeuroCom Balance Manager System ® static posturography device to assess static balance, which is objective evaluating system.
The system compare the values reported for participants assessment then compare them to pre-recorded data base.
The values of the test is assessed according to the percentage to the normal (average) values matched with the age group and gender.
Above 80% determined as normal, and below this value determine balance disturbance.
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2 Months
|
Collaborators and Investigators
Sponsor
Investigators
- Principal Investigator: AYSEL yildiz, Ass. Prof., Marmara University
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
Additional Relevant MeSH Terms
Other Study ID Numbers
- 09.2020.897
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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