- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06519305
Examination of Musculoskeletal System Problems, Pain and Quality of Life Related to Working Conditions in Chiropractors
March 7, 2025 updated by: AYCAN ÇAKMAK REYHAN, Istanbul Bilgi University
This research aims to investigate musculoskeletal problems and pain, as well as their effects on the quality of life, arising from the working conditions of chiropractors in their workplaces.
Additionally, it is intended to conduct a detailed analysis of working conditions in chiropractors' work environments to identify existing problems, establish the cause-and-effect relationship between musculoskeletal problems, pain, and these conditions, conduct studies to improve chiropractors' work environments, and demonstrate the positive effects of improving working conditions on the quality of life and professional performance of chiropractors.
Within this scope, the physical layout of chiropractors' work environments, ergonomic factors, and workplace conditions will be analyzed.
Musculoskeletal problems experienced by chiropractors will be identified, and research will be conducted on pain and musculoskeletal disorders associated with workplace factors.
Furthermore, the effects of working conditions on the quality of life of chiropractors will be evaluated.
Study Overview
Status
Completed
Conditions
Intervention / Treatment
Study Type
Observational
Enrollment (Actual)
30
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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Istanbul, Turkey
- Istanbul Bilgi 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
Accepts Healthy Volunteers
Yes
Sampling Method
Probability Sample
Study Population
Professionals actively working as chiropractors
Description
Inclusion Criteria:
- Male and female physiotherapists between the ages of 25-45, with at least 1 year of chiropractic experience, will be selected
Exclusion Criteria:
- Having practiced chiropractic for less than 1 year.
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
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
The Visual Analog Scale (VAS)
Time Frame: 1 mount
|
VAS is a measurement tool commonly used to assess subjective characteristics or experiences, particularly pain intensity.
It typically consists of a straight line, usually 10 centimeters in length, with one end representing the extreme of the characteristic being measured (e.g., "no pain" or "worst pain imaginable") and the other end representing the opposite extreme.
Participants are asked to mark on the line the point that best represents their experience.
This mark's distance from the zero point (e.g., "no pain") is then measured to quantify the characteristic being assessed.
For pain intensity, the distance marked by the participant correlates with the severity of their pain, with longer distances indicating more severe pain.
The VAS is a simple yet effective tool for quantifying subjective experiences and is widely used in clinical settings and research studies to assess various factors such as pain intensity, mood, and well-being.
|
1 mount
|
|
SF-36 Short Form 36 Health Survey,
Time Frame: 1 mount
|
The SF-36, or Short Form 36, is a widely used questionnaire designed to assess an individual's health-related quality of life.
It consists of 36 questions that cover eight different health domains: physical functioning, role limitations due to physical health problems, bodily pain, general health perceptions, vitality (energy/fatigue), social functioning, role limitations due to emotional problems, and mental health (psychological distress and psychological well-being).
Each domain is scored separately, and the scores can be aggregated to produce two summary measures: the Physical Component Summary (PCS) and the Mental Component Summary (MCS).
These summary measures provide an overall assessment of physical and mental health status, respectively.
The SF-36 is a valuable tool in clinical research and healthcare settings for evaluating patients' overall health status, tracking changes over time, and comparing different patient populations.
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1 mount
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
The Beck Depression Inventory (BDI)
Time Frame: 1 mount
|
BDI), also known as the Beck Depression Scale, is a self-report questionnaire designed to measure the severity of depression symptoms in individuals.
Beck, the BDI consists of 21 items that assess various symptoms commonly associated with depression, such as sadness, guilt, fatigue, changes in appetite or sleep patterns, and suicidal thoughts.Each item on the scale presents a statement describing a particular symptom, and individuals are asked to rate how much they have been experiencing each symptom over a specific time frame, typically the past two weeks.
Responses are scored on a scale ranging from 0 to 3, with higher scores indicating greater severity of depressive symptoms.The total score on the BDI provides an overall measure of depression severity, with higher scores indicating more severe depression.
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1 mount
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Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
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)
April 25, 2024
Primary Completion (Actual)
May 25, 2024
Study Completion (Actual)
June 25, 2024
Study Registration Dates
First Submitted
July 19, 2024
First Submitted That Met QC Criteria
July 19, 2024
First Posted (Actual)
July 25, 2024
Study Record Updates
Last Update Posted (Actual)
March 25, 2025
Last Update Submitted That Met QC Criteria
March 7, 2025
Last Verified
March 1, 2025
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- IstanbulBuu
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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