Analyzing Postural Parameters in Physiotherapy and Rehabilitation Students

January 6, 2026 updated by: Asude ARIK, Hacettepe University

Examining The Effect of Physical Workload on Postural Parameters in Physiotherapy and Rehabilitation Students

In our study, with the voluntary participation of Term 3 and Term 4 students from the Hacettepe University Faculty of Physiotherapy and Rehabilitation, we examined the effect of physical workload on postural parameters based on students' standing and sitting times. Additionally, through surveys, we assessed the students' physical activity levels, quality of life, sleep, and burnout levels. The aim was to investigate the relationship between these components and postural alignment by measuring their levels. By identifying the factors that may affect students' postural alignment, the study aims to determine potential risks and provide valuable information for physiotherapists, physiotherapy students, and educators.

Study Overview

Status

Completed

Detailed Description

Volunteer individuals among Term 4 (senior year) intern physiotherapist students and Term 3 students studying at Hacettepe University Faculty of Physical Therapy and Rehabilitation will be included in the study. Individuals who will be included in the study will be informed face to face about the purpose of the research, the evaluation methods to be used in the research, and the results we foresee, as well as what benefits we will provide to the individuals at the end of the study. Participants will be reached via posters/brochures. Individuals participating in the study will be informed about the surveys and the parameters to be evaluated at the first meeting. Postural evaluations of individuals will be carried out 4 times, on Mondays and Fridays, in the morning and in the evening, for 1 week. Questionnaires will be asked to be answered after the first and last posture evaluation. The number of individuals to be included in our study was calculated using the G*Power 3.1 program, taking the effect size as 0.74, alpha type error rate as 0.05 and the power of the test as 0.80, and the sample size for the period 4 and period 3 research groups was determined as 37/37. Taking into account situations such as inability to continue working, a total of 74 individuals were planned to be included in the study, with an excess of 10%.

Study Type

Observational

Enrollment (Actual)

74

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

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

Volunteer individuals from Term 4 (senior year) intern physiotherapist students and Term 3 students studying at Hacettepe University Faculty of Physical Therapy and Rehabilitation will be included in the study.

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

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 assessment
Time Frame: Up to four weeks
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.
Up to four weeks

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Musculoskeletal assessment
Time Frame: Baseline

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
Physical activity assessment
Time Frame: Baseline

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:

  • Active: Above 3000 MET-min/week
  • Moderately active: Between 600 and 3000 MET-min/week
  • Inactive: Below 600 MET-min/week
Baseline
Anxiety level assessment
Time Frame: Baseline

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.

  • High scores (60-80) indicate high anxiety levels.
  • Moderate scores (40-59) indicate moderate anxiety levels.
  • Low scores (20-39) indicate low anxiety levels.
Baseline
Sleep quality and disorder assessment
Time Frame: Baseline

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:

  1. Subjective Sleep Quality
  2. Sleep Latency
  3. Sleep Duration
  4. Habitual Sleep Efficiency
  5. Sleep Disturbances
  6. Use of Sleep Medication
  7. Daytime Dysfunction Each component is scored between 0 and 3, and the total score ranges from 0 to 21.

    • A total score above 5 indicates poor sleep quality.
    • A higher total score reflects worsening sleep quality.
Baseline
Burnout level assessment
Time Frame: Baseline

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:

  • Emotional Exhaustion (9 items)
  • Depersonalization (5 items)
  • Personal Accomplishment (8 items)

Each item is scored on a scale from 0 to 4, where:

  • 0 = Never
  • 1 = A few times a year
  • 2 = A few times a month
  • 3 = A few times a week
  • 4 = Every day After scoring, each subscale's total score is calculated separately.
  • Higher scores in Emotional Exhaustion and Depersonalization indicate higher levels of burnout.
  • Higher scores in Personal Accomplishment indicate lower levels of burnout.
Baseline
Quality Of Life Level assessment
Time Frame: Baseline
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.
Baseline

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

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

The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the 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)

October 2, 2025

Primary Completion (Actual)

November 27, 2025

Study Completion (Actual)

January 6, 2026

Study Registration Dates

First Submitted

October 28, 2024

First Submitted That Met QC Criteria

February 24, 2025

First Posted (Actual)

February 28, 2025

Study Record Updates

Last Update Posted (Actual)

January 8, 2026

Last Update Submitted That Met QC Criteria

January 6, 2026

Last Verified

January 1, 2026

More Information

Terms related to this study

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

product manufactured in and exported from the U.S.

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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