CClinicalTrials.gg
CompletedNCT07739836Updated Sep 30, 2026

Effects of Physical Use Characteristics During Academic Education on Musculoskeletal Function and Body Awareness in University Students From Different Academic Departments

An observational study in Physiotherapy and Rehabilitation Department Students & Architecture Department Students, sponsored by Health Institutes of Turkey. Completed at 1 site in Turkey (Türkiye). Open to participants aged 18 Years to 25 Years, including healthy volunteers. Per ClinicalTrials.gov, last updated 2026-09-30.

Sponsored by Health Institutes of Turkey · Observational

Updated Sep 30, 2026Now CompletedEnrollment updatedGo to Updates ↓
Study type
Observational
Model
Other
Time perspective
Cross-sectional
Enrollment
300
Ages
18 Years to 25 Years
Sex
All
01

Study summary

Aim of the study is to compare the levels of spinal stabilization, posture, deep neck flexor muscle endurance, and body awareness of physiotherapy and rehabilitation students and architecture students, whose academic training processes and professional practices are different but intensive, and who possess different physical usage characteristics in these processes, and to reveal the effects of professional training content on the musculoskeletal system.

Read the detailed description

The aim of this study is to compare the levels of spinal stabilization, posture, deep neck flexor muscle endurance, and body awareness of physiotherapy and rehabilitation students and architecture students, whose academic training processes and professional practices are different but intensive, and who possess different physical usage characteristics in these processes, and to reveal the effects of professional training content on the musculoskeletal system. The study plans to include volunteer students studying in the 2nd year and above in both the physiotherapy and rehabilitation and architecture departments. This research study is designed as an observational and cross sectional evaluation study.

02

Conditions studied

  • Physiotherapy and Rehabilitation Department Students & Architecture Department Students
03

In context

Lead sponsor

Health Institutes of Turkey is the lead sponsor of 18 studies on the registry; 1 is open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years to 25 Years
Sexes eligible
All
Accepts healthy volunteers
Yes
Sampling method
Non-probability sample

Study population

Physiotherapy and Rehabilitation Department Students \& Architecture Department Students

Inclusion criteria

  • Being a university student aged 18-25.
  • Being a second-year or higher student in the Physiotherapy and Rehabilitation Department (n=150).
  • Being a second-year or higher student in the Architecture Department (n=150).
  • Having a daily screen time (computer, tablet, mobile phone) of ≥ 3 hours.
  • Agreeing to participate in the study voluntarily.

Exclusion criteria

Exclusion Criteria:

  • Having a diagnosis of surgery or serious injury in the cervical, thoracic, or lumbar region within the last 6 months.
  • Individuals with diagnosed musculoskeletal, neurological, or vestibular system pathologies.
  • Individuals with orthopedic deformities that may affect posture (e.g., scoliosis >20° Cobb angle).
  • Professional athletes or individuals who regularly engage in strength training.
05

Study design

Observational model
Other
Time perspective
Cross-sectional
Enrollment
300 participants (actual)
Patient registry
No

Groups and cohorts

  • Group I

    Physiotherapy and Rehabilitation Department Students

  • Group II

    Architecture Department Students

06

What researchers measure

Primary outcomes

  1. Multifidus Muscle Stabilization Assessment

    A Biofeedback Stabilizer pressure feedback device will be used to determine the stabilization and activation value of the multifidus muscle. Prior to the test, all participants will be taught the abdominal hallowing maneuver. While participants lie supine, the stabilizer device will be placed in the lumbar region. The Biofeedback device will be set to 70 mmHg, and the participant will be asked to perform the abdominal hallowing maneuver without moving the spine and pelvis, maintaining the contraction for at least 10 seconds.

    Time frame: Baseline

  2. New York Posture Rating Chart

    This assessment will score postural changes in 13 different areas of the body. A score of 5 points will be given for correct postural structure, 3 points for moderate abnormalities, and 1 point for severe abnormalities. A score between 13 and 65 will be obtained on the scale. A score of 45 and above will be classified as "Very Good," 40-44 as "Good," 30-39 as "Moderate," 20-29 as "Poor," and 19 and below as "Poor" posture.

    Time frame: Baseline

  3. Deep Neck Flexor Endurance Test

    This test will be used to assess deep flexor muscle endurance in the cervical region. The test will be performed in a supine hook position. The participant's hands will be placed loosely on their abdomen. The participant will be asked to pull their chin inward (chin tuck) and, while maintaining this position, lift their head off the bed (approximately 2.5 cm). They will be asked to maintain this position for as long as possible without breaking it, and the time spent in this position will be recorded in seconds.

    Time frame: Baseline

  4. Body Awareness Questionnaire (BAQ)

    BAQ is an 18-item self-report scale designed to measure how attentive you are to normal, non-emotional internal bodily processes. It evaluates your sensitivity to everyday bodily cycles (like sleep and hunger), ability to detect subtle changes, and capacity to anticipate physical reactions. Typically takes about 3 to 5 minutes. Items are generally rated on a 1 to 7 scale, with higher total scores indicating greater perceived conNdence and accuracy in monitoring your physical state over time.

    Time frame: Baseline

07

Study locations

1 site
  • Haliç Üniversitesi
    Istanbul, Turkey (Türkiye)
08

Updates

1 registry update since Sep 25, 2026
Status
Recruiting→Completed
changed Sep 30, 2026
Show all 1 update
  1. Sep 30, 2026
    Recruiting→Completed
    + 3 other changes: date precision, contact details and site details

From the registry record's own update history. This site started tracking changes on Sep 25, 2026; for anything earlier, see the record history on ClinicalTrials.gov ↗

09

Registry details

Key details

Study ID
NCT07739836
Lead sponsor
Health Institutes of Turkey
Responsible party
Ezgi Türkmen (Principal Investigator, R&D Specialist, PhD, Health Institutes of Turkey) — Principal investigator
First posted
Jul 31, 2026
Start date
Aug 4, 2026
Primary completion
Sep 29, 2026
Completion
Sep 29, 2026
Last update
Sep 30, 2026

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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This study is completed, as verified in Jul 2026. You cannot join it, but the record below documents what was studied.

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