- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06360198
The Relationship Between Posture, Sense of Position, Musculoskeletal Discomfort and Anxiety
April 7, 2024 updated by: Ankara Yildirim Beyazıt University
The Relationship Between Posture, Sense of Position, Musculoskeletal Discomfort and Anxiety in Asymptomatic Individuals: A Cross-Sectional Study
It is known that posture is affected by various factors such as somatosensation, visual perception and cognition.
In addition, it is also thought to affect conditions such as stress and anxiety through receptors.
The aim of this study was to investigate the relationship between postural changes such as thoracic kyphosis, musculoskeletal problems, trunk position sense and anxiety in young individuals who were asymptomatic in terms of musculoskeletal problems.
Study Overview
Status
Completed
Intervention / Treatment
Study Type
Observational
Enrollment (Actual)
67
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
-
-
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Ankara, Turkey
- Ankara Yıldırım Beyazıt University
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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
- Older Adult
Accepts Healthy Volunteers
Yes
Sampling Method
Non-Probability Sample
Study Population
Young people who are asymptomatic in terms of musculoskeletal problems
Description
Inclusion Criteria:
- 18 years and older
- Volunteered to participate in the study
- No systemic or neurological disease
Exclusion Criteria:
- Severe visual and hearing problems
- Orthopedic injury or surgery in the last 6 months
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 |
|---|---|
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Group 1
The only group of this cross-sectional observational study consists of individuals over the age of 18.
There were no orthopedic and neurological chronic diseases included.
Individuals with severe visual and hearing problems and individuals who had undergone surgery within the last 6 months were excluded.
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No intervention was applied to the group.
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
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Throcic Kyphosis
Time Frame: Baseline
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The thoracic kyphosis angle was evaluated with a dual digital inclinometer (Acumar, Lafeyette, USA).
Repetitive cervical flexion, extension and lateral flexion movements were asked from the subjects before the measurement.
They were also asked to perform back rotation of the shoulders and to take a deep breath in and out.
Subsequently, they were asked to stand in a normal position in which they were comfortable and the measurement was performed.
The inclinometer was placed on the T1-2 and T12-L1 vertebrae.
The value on the inclinometer screen was noted as the degree of kyphosis.
A kyphosis angle of 20-40 degrees is considered normal.
Values above 45 degrees are considered as hyperkyphosis.
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Baseline
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Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
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Trunk Position Sense
Time Frame: Baseline
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Trunk position sense was evaluated with a dual digital inclinometer (Acumar, Lafeyette, USA) during 30 degrees of trunk flexion.
For the measurement, the subjects were asked to stand in a standing and comfortable position.
The inclinometer was placed on the T1 and S1 vertebrae.
Individuals were asked to perform 30 degrees of trunk flexion with their eyes closed.
The measurement was taught by performing 2 trials.
Then, the individuals were asked to find the target angle that was taught.
The angle that the individuals thought was the target angle was recorded.
The difference between the recorded angle and the target angle was written as absolute value.
The process was repeated three times and averaged.
There is no specific reference value for trunk flexion position sensation.
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Baseline
|
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Musculoskeletal Discomfort
Time Frame: Baseline
|
Musculoskeletal disorders of the individuals were assessed with the Cornell Musculoskeletal Disorder Scale.
The scale consists of three categories assessing the frequency, severity and work intervention of musculoskeletal discomfort in 20 different body parts within a week.
The answers given in the frequency section are scored between 0-1.5-3.5-5-10.
In the severity of musculoskeletal discomfort and the work disability caused by the musculoskeletal system disorder sections the answers are scored between 1-3.
The scores for each body part are multiplied and then summed to obtain a total score from the three sections.
The total score is the sum of all section scores.
A lower score indicates less musculoskeletal discomfort.
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Baseline
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Anxiety
Time Frame: Baseline
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Anxiety of the individuals was assessed with the Generalised Anxiety Disorder-7 scale.
The scale evaluates the experiences in the last 2 weeks.
The Generalised Anxiety Disorder-7 scale is a four-point Likert-type scale based on self-report.
The total score is obtained by adding the score of the answer given to each item.
The higher the total score obtained from the scale, the higher the level of anxiety.
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Baseline
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Collaborators and Investigators
This is where you will find people and organizations involved with this study.
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)
June 30, 2022
Primary Completion (Actual)
November 30, 2022
Study Completion (Actual)
December 30, 2022
Study Registration Dates
First Submitted
April 7, 2024
First Submitted That Met QC Criteria
April 7, 2024
First Posted (Actual)
April 11, 2024
Study Record Updates
Last Update Posted (Actual)
April 11, 2024
Last Update Submitted That Met QC Criteria
April 7, 2024
Last Verified
April 1, 2024
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- 2022-874/08
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
NO
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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