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

4 agosto 2026 aggiornato da: Ezgi Türkmen, Health Institutes of Turkey

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.

Panoramica dello studio

Stato

Reclutamento

Condizioni

Physiotherapy and Rehabilitation Department Students & Architecture Department Students

Descrizione dettagliata

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.

Tipo di studio

Osservativo

Iscrizione (Stimato)

300

Contatti e Sedi

Questa sezione fornisce i recapiti di coloro che conducono lo studio e informazioni su dove viene condotto lo studio.

Contatto studio

Nome: Ezgi Türkmen
Numero di telefono: 0090 216 547 26 00
Email: turkmnezgi@gmail.com

Luoghi di studio

Turchia (Türkiye)
- - Istanbul, Turchia (Türkiye)
    - Reclutamento
    - Haliç Üniversitesi
    - Contatto:
      
      Ayşenur Çetinkaya
      
      Numero di telefono: 0090 212 924 24 44
      
      Email: aysenurcetinkaya@halic.edu.tr

Criteri di partecipazione

I ricercatori cercano persone che corrispondano a una certa descrizione, chiamata criteri di ammissibilità. Alcuni esempi di questi criteri sono le condizioni generali di salute di una persona o trattamenti precedenti.

Criteri di ammissibilità

Età idonea allo studio

Adulto

Accetta volontari sani

Sì

Metodo di campionamento

Campione non probabilistico

Popolazione di studio

Physiotherapy and Rehabilitation Department Students & Architecture Department Students

Descrizione

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:

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.

Piano di studio

Questa sezione fornisce i dettagli del piano di studio, compreso il modo in cui lo studio è progettato e ciò che lo studio sta misurando.

Come è strutturato lo studio?

Dettagli di progettazione

Numero di gruppi/coorti

Coorti e interventi

Gruppo / Coorte
Group I Physiotherapy and Rehabilitation Department Students
Group II Architecture Department Students

Cosa sta misurando lo studio?

Misure di risultato primarie

Misura del risultato	Misura Descrizione	Lasso di tempo
Multifidus Muscle Stabilization Assessment Lasso di tempo: Baseline	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.	Baseline
New York Posture Rating Chart Lasso di tempo: Baseline	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.	Baseline
Deep Neck Flexor Endurance Test Lasso di tempo: Baseline	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.	Baseline
Body Awareness Questionnaire (BAQ) Lasso di tempo: Baseline	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.	Baseline

Collaboratori e investigatori

Qui è dove troverai le persone e le organizzazioni coinvolte in questo studio.

Sponsor

Health Institutes of Turkey

Studiare le date dei record

Queste date tengono traccia dell'avanzamento della registrazione dello studio e dell'invio dei risultati di sintesi a ClinicalTrials.gov. I record degli studi e i risultati riportati vengono esaminati dalla National Library of Medicine (NLM) per assicurarsi che soddisfino specifici standard di controllo della qualità prima di essere pubblicati sul sito Web pubblico.

Studia le date principali

Inizio studio (Effettivo)

4 agosto 2026

Completamento primario (Stimato)

1 settembre 2026

Completamento dello studio (Stimato)

1 settembre 2026

Date di iscrizione allo studio

Primo inviato

28 luglio 2026

Primo inviato che soddisfa i criteri di controllo qualità