- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT07314710
Factors Affecting Postural Awareness in Academics
January 3, 2026 updated by: Lütfiye AKKURT, MSc, Kutahya Health Sciences University
Factors Affecting Postural Awareness in Academics in Kütahya
The aim of the study is to determine the factors affecting postural awareness in academics.
Study Overview
Status
Completed
Conditions
Detailed Description
The aim of the study is to determine the factors affecting postural awareness in academics.
Data on age, height, weight, body mass index, gender, duration of academic work, daily working time, and distance from the eye to the screen were collected.
Postural awareness, mindfulness, fatigue, and posture measures are described below.
Postural Awareness Scale, Mindfulness Attention Awareness Scale, Chalder Fatigue Scale and New York Posture Rating scale were used in study.
Study Type
Observational
Enrollment (Actual)
122
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
-
-
Kütahya
-
Kütahya, Kütahya, Turkey (Türkiye), (552) 266-8356
- Kutahya Health Sciences University
-
-
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
No
Sampling Method
Probability Sample
Study Population
Academics in Kütahya Health Sciences University
Description
Inclusion Criteria:
- Being an academician
- Being between 24 and 60 years old and People and pregnant women were excluded from the study.
Exclusion Criteria:
- Having with any orthopaedic or neurological disorders
- Being pregnant
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 |
|---|---|---|
|
Postural Awareness Scale
Time Frame: At the beginning of the study
|
The Postural Awareness Scale (PAS) was designed by Cramer et al. 1 to measure self-reported awareness of body posture, and translated to Turkish version by Dursun et al..
The PAS consist of 12 items in original form but 12th item was removed from the Turkish version due to factor load was low.
The PAS consist of two factor structures, ease/familiarity with postural awareness (items 6-11) and need for attention regulation with postural awareness (items 1-5).
The Turkish version of PAS scores range from 11 to 77, higher scores indicate high greater postural awareness.
The total score was calculated after reversing the values of items 1, 2, 3, 4, 5 and adding other items.
|
At the beginning of the study
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Mindfulness Attention Awareness Scale
Time Frame: At the beginning of the study
|
The Mindfulness Attention Awareness Scale (MAAS) was developed by Brown and Ryan 3 and translated to Turkish version by Özyeşil et al.
The MAAS contains 15 items to measure individual differences in the tendency to be mindful.
All the items are scored range from 1 (almost never) to 6 (almost always) points.
The MAAS total scores can range from 1 to 6 points due to based on a mean (average) of the 15 items.
Higher scores indicate a higher level of mindfulness.
|
At the beginning of the study
|
|
Chalder Fatigue Scale
Time Frame: At the beginning of the study
|
The Chalder Fatigue Scale (CFS) was developed by Chalder et al. 5 and translated to Turkish version by Adın et al.
The CFS measures the severity of perceived fatigue and chronicity of fatigue.
The CFS consist of 11 items, and which consist of two dimensions, including physical (CFS-PF) and mental fatigue (CFS-MF).
The total score ranges from 0 to 33 points.
Higher scores indicates a high level of fatigue.
|
At the beginning of the study
|
|
New York Posture Rating Scale
Time Frame: At the beginning of the study
|
The New York Posture Rating (NYPR) Scale was used to assess postural alignment changes for clinical postural evaluation in 13 body aligment segment.
Lateral and posterior posture analysis is performed in 13 regions (head, neck, shoulder, scapula, upper thoracic, waist, rips, abdomen, hips, knees, legs, feet and toes).
Every region was scored 1 (pronounced deviation), 3 (slight deviation) or 5 (correct posture) points.
Total score is between 13-65 points.
Higher scores indicates better the postural alignment.
|
At the beginning of the study
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Investigators
- Principal Investigator: Lütfiye AKKURT, PhD, Kutahya Health Sciences University
- Study Chair: Nisa TÜRÜTGEN, MSc, Kutahya Health Sciences University
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)
September 1, 2025
Primary Completion (Actual)
December 10, 2025
Study Completion (Actual)
December 18, 2025
Study Registration Dates
First Submitted
December 18, 2025
First Submitted That Met QC Criteria
December 18, 2025
First Posted (Estimated)
January 2, 2026
Study Record Updates
Last Update Posted (Actual)
January 6, 2026
Last Update Submitted That Met QC Criteria
January 3, 2026
Last Verified
December 1, 2025
More Information
Terms related to this study
Keywords
Other Study ID Numbers
- 2025/11-29
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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