- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06851780
Analyzing Postural Parameters in Physiotherapy and Rehabilitation Students
Examining The Effect of Physical Workload on Postural Parameters in Physiotherapy and Rehabilitation Students
Study Overview
Status
Conditions
Detailed Description
Study Type
Enrollment (Actual)
Contacts and Locations
Study Locations
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Ankara, Turkey (Türkiye)
- Hacettepe University
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Adult
Accepts Healthy Volunteers
Sampling Method
Study Population
Description
Inclusion Criteria:
- Individuals who volunteer to participate in the study,
- Individuals who did not have pain according to the NORDIC Extended Musculoskeletal System questionnaire at the time of the evaluations,
Exclusion Criteria:
- Being diagnosed with scoliosis by a physician,
- Having spinal cord or extremity pain diagnosed by a physician in the last 3 months,
- Being diagnosed with any developmental disorder (Scheuermann's/Calve Disorder etc.),
- Having limb inequality, spine and pelvis etc. having serious deformities,
- Getting diagnosed with Infection (Spinal Tuberculosis etc.), Tumor (Multiple Myeloma),
- Having had spine surgery,
- Having a systemic inflammatory disease,
- Being diagnosed with a neurological and/or cognitive disease that may affect cognitive functions,
- Epilepsy, Antidepressant / Attention enhancing drug use,
- Being diagnosed with Cardiorespiratory Disease,
- Having menstrual irregularity,
Study Plan
How is the study designed?
Design Details
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
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Postural assessment
Time Frame: Up to four weeks
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Participants' postures will be evaluated using the Diers Formetric-4D system (DIERS International GmbH; Schlangenbad, Germany) operating with the Dicam 3v3.11 software.
In this method, white light raster lines are projected onto the individual's back, and the deformation of these lines due to the 3D shape of the back is captured by a camera.
The software detects convex and concave regions, allowing for the immediate identification of anatomical landmarks and fixed points.
Using a mathematical algorithm, the system reconstructs a 3D model of the spine.During the measurement, participants will be positioned in a relaxed, motionless stance, standing on both feet, with their arms hanging freely, facing forward, and their backs turned toward the camera.
Their heels will be placed on a marked area on the platform to ensure standard positioning.
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Up to four weeks
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Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Musculoskeletal assessment
Time Frame: Baseline
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The Extended Nordic Musculoskeletal questionnarie will be used for the evaluation of musculoskeletal system. This questionnaire is used to identify musculoskeletal disorders and evaluates the body in nine regions: neck, shoulders, back, elbows, wrists/hands, lower back, hips/thighs, knees, and ankles/feet. It provides information on the onset, frequency, and consequences of musculoskeletal pain. The questionnaire first asks about the presence of pain or discomfort in these nine body regions. If the participant answers "yes", they proceed to the relevant follow-up questions. The Extended Nordic Musculoskeletal Questionnaire (NMQ-E) assesses whether pain, discomfort, or aches have been experienced at any time in life, in the past 12 months, in the past four weeks, and on the day of assessment. |
Baseline
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Physical activity assessment
Time Frame: Baseline
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The International Physical Activity questionnaire will be used for the evaluation of physical activity. The short version of the International Physical Activity Questionnaire (IPAQ-SF) will be used to determine the type of physical activity an individual has performed in the past 7 days and the time spent on these activities. The total score will be calculated by multiplying the duration (minutes) and frequency (days) of walking, moderate, and vigorous activities. Participants will be classified based on their Metabolic Equivalent of Task (MET) score as follows:
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Baseline
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Anxiety level assessment
Time Frame: Baseline
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The State-Trait Anxiety Inventory (STAI-1 and STAI-2) will be used for the evaluation of anxiety level. The STAI consists of 40 statements divided into two subscales: State Anxiety (STAI-1) and Trait Anxiety (STAI-2), each containing 20 items. It is a self-assessment questionnaire based on a 4-point Likert scale.
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Baseline
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Sleep quality and disorder assessment
Time Frame: Baseline
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The Pittsburgh Sleep Quality Index will be used for the evaluation of sleep quality and disorder. The Pittsburgh Sleep Quality Index (PSQI) is a 24-item questionnaire designed to assess sleep quality and disturbances over the past month. Among these, 19 questions are self-reported, while 5 questions are answered by the spouse or roommate. Only 18 questions are scored, categorized into 7 components:
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Baseline
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Burnout level assessment
Time Frame: Baseline
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The malsach Burnout Inventory will be used for the evaluation of burnout level. The Maslach Burnout Inventory (MBI) is a 5-point Likert-type scale consisting of 22 items designed to assess occupational burnout. It is divided into three subscales:
Each item is scored on a scale from 0 to 4, where:
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Baseline
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Quality Of Life Level assessment
Time Frame: Baseline
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The SF-36 Quality of Life Scale will be used for the evaluation of quality of life level.
The Short Form-36 (SF-36) is a widely used self-reported health assessment questionnaire consisting of 36 questions across eight subscales: Physical Functioning, Role Limitations, Social Functioning, Mental Health, Vitality, Pain, and General Health.
Each subscale is scored separately, and the total score ranges from 0 to 100.
A higher score indicates a better health status and greater improvement in overall well-being.
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Baseline
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Collaborators and Investigators
Sponsor
Investigators
- Study Chair: Yeliz Gülce TANIMLI, Hacettepe University
- Study Chair: Büşra ERGİT, Hacettepe University
- Study Chair: Zafer ERDEN, Prof, Hacettepe University
- Study Chair: Esra ATEŞ NUMANOĞLU, PhD, Hacettepe University
- Principal Investigator: Asude ARIK, PhD, Hacettepe University
Publications and helpful links
General Publications
- Korakakis V, O'Sullivan K, O'Sullivan PB, Evagelinou V, Sotiralis Y, Sideris A, Sakellariou K, Karanasios S, Giakas G. Physiotherapist perceptions of optimal sitting and standing posture. Musculoskelet Sci Pract. 2019 Feb;39:24-31. doi: 10.1016/j.msksp.2018.11.004. Epub 2018 Nov 17.
- Sorensen CJ, Norton BJ, Callaghan JP, Hwang CT, Van Dillen LR. Is lumbar lordosis related to low back pain development during prolonged standing? Man Ther. 2015 Aug;20(4):553-7. doi: 10.1016/j.math.2015.01.001. Epub 2015 Jan 14.
- Degenhardt BF, Starks Z, Bhatia S. Reliability of the DIERS Formetric 4D Spine Shape Parameters in Adults without Postural Deformities. Biomed Res Int. 2020 Feb 13;2020:1796247. doi: 10.1155/2020/1796247. eCollection 2020.
- Poitras S, Blais R, Swaine B, Rossignol M. Management of work-related low back pain: a population-based survey of physical therapists. Phys Ther. 2005 Nov;85(11):1168-81.
- Andersen JH, Haahr JP, Frost P. Risk factors for more severe regional musculoskeletal symptoms: a two-year prospective study of a general working population. Arthritis Rheum. 2007 Apr;56(4):1355-64. doi: 10.1002/art.22513.
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
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- SBA 23/427
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
product manufactured in and exported from the U.S.
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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