- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05982964
Impact of Scapula Position on Functionality and Balance in People With Chronic Low Back Pain
Study Overview
Status
Conditions
Detailed Description
Study Type
Enrollment (Actual)
Contacts and Locations
Study Locations
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None Selected
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Istanbul, None Selected, Turkey, 34353
- Hazal GENÇ
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Adult
- Older Adult
Accepts Healthy Volunteers
Sampling Method
Study Population
Description
Inclusion criteria:
- Individuals between the ages of 18-65
- Individuals with low back pain for at least 3 months for the first group
- Not undergoing surgery related to the lumbar region
- Cases without lumbar steroid injection in the last 3 months
- Not having visual and hearing loss
- Having low back pain
- Cases without neurological problems
- Cases without tumor and infection in the lumbar region
- Exclusion criteria:
- Individuals under the age of 18
- Individuals with low back pain for less than 3 months for the first group
- Not having a musculoskeletal or neuromuscular disease that limits mobility,
Study Plan
How is the study designed?
Design Details
Cohorts and Interventions
Group / Cohort |
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Healthy volunteers
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back pain group
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Pressure Pain Threshold Algometer
Time Frame: 1 day
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The pressure algometer is a tool used to assess the pain threshold.
The algometer used in this study is connected to a dial measuring the pressure in kilograms and pounds, and consists of a metal piston with a diameter of 1 centimeter at the tip, the smallest gap of which is 100 gr and 10 kg/cm².
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1 day
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Examining the Scapular Position
Time Frame: 1 day
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The lateral scapular glide test was used to evaluate the scapula position.
In the first position, the arms were relaxed at the sides, the shoulder was in the neutral position, in the second position the patient's hands were positioned around the waist and the humerus was brought to medial rotation and abduction of 45 degrees, and in the third position, the humerus was placed in maximal medial rotation and 90-degree abduction.
|
1 day
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Evaluation of Balance
Time Frame: 1 day
|
The static and dynamic postural stability of all individuals included in the study were evaluated with the Biodex Balance System (BDS). For dynamic stability measurement, a total of 3 tests were conducted, with the platform in dynamic position, with each period lasting 20 seconds, giving the participant a rest period of 10 seconds in between. Afterwards, the average of these 3 tests was obtained automatically by the device. In the results obtained, it is possible to interpret that as the score approaches 0, the balance is maintained, and as it moves away from 0, the balance is deteriorated. |
1 day
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Proprioception Evaluation
Time Frame: 1 day
|
An inclinometer is an instrument that records angular movements with respect to gravity. The inclinometer has many advantages such as precise measurement, digital display, and ease of use. In our study, inclinometer was used in the evaluation of proprioception. Measurements will be recorded in degrees. |
1 day
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Evaluation of Functionality
Time Frame: 1 day
|
The Oswestry Low Back Pain Disability Questionnaire (OBAEA) was used to examine functionality in patients with chronic low back pain.
This survey consists of 10 questions in total.
Each question has 6 options and ranges from 0 to 5. Participants are asked to mark the option that best fits their individual situation.
While 50 is the highest score, it is evaluated as mild functional disability between 1 and 10 points, moderate functional disability between 11 and 30 points, and severe functional disability between 31 and 50 points.
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1 day
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Waist Awareness Assessment
Time Frame: 1 day
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Fremantle Waist Awareness Questionnaire was used to evaluate low back awareness in the study.
The Fremantle Waist Awareness Questionnaire is the only one that assesses body awareness about the waist.
It consists of 9 questions in total and each question has a score ranging from 0-4.
In total, the lowest 0 and the highest 36 points can be obtained.
High scores indicate low back awareness.
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1 day
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Collaborators and Investigators
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
- E-85646034-604.02.02-62452
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
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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