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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 augustus 2026 bijgewerkt door: 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.
Studie Overzicht
Toestand
Werving
Gedetailleerde beschrijving
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.
Studietype
Observationeel
Inschrijving (Geschat)
300
Contacten en locaties
In dit gedeelte vindt u de contactgegevens van degenen die het onderzoek uitvoeren en informatie over waar dit onderzoek wordt uitgevoerd.
Studiecontact
- Naam: Ezgi Türkmen
- Telefoonnummer: 0090 216 547 26 00
- E-mail: turkmnezgi@gmail.com
Studie Locaties
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Istanbul, Turkije (Türkiye)
- Werving
- Haliç Üniversitesi
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Contact:
- Ayşenur Çetinkaya
- Telefoonnummer: 0090 212 924 24 44
- E-mail: aysenurcetinkaya@halic.edu.tr
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Deelname Criteria
Onderzoekers zoeken naar mensen die aan een bepaalde beschrijving voldoen, de zogenaamde geschiktheidscriteria. Enkele voorbeelden van deze criteria zijn iemands algemene gezondheidstoestand of eerdere behandelingen.
Geschiktheidscriteria
Leeftijden die in aanmerking komen voor studie
- Volwassen
Accepteert gezonde vrijwilligers
Ja
Bemonsteringsmethode
Niet-waarschijnlijkheidssteekproef
Studie Bevolking
Physiotherapy and Rehabilitation Department Students & Architecture Department Students
Beschrijving
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.
Studie plan
Dit gedeelte bevat details van het studieplan, inclusief hoe de studie is opgezet en wat de studie meet.
Hoe is de studie opgezet?
Ontwerpdetails
Cohorten en interventies
Groep / Cohort |
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Group I
Physiotherapy and Rehabilitation Department Students
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Group II
Architecture Department Students
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Wat meet het onderzoek?
Primaire uitkomstmaten
Uitkomstmaat |
Maatregel Beschrijving |
Tijdsspanne |
|---|---|---|
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Multifidus Muscle Stabilization Assessment
Tijdsspanne: 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.
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Baseline
|
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New York Posture Rating Chart
Tijdsspanne: 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.
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Baseline
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Deep Neck Flexor Endurance Test
Tijdsspanne: 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
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Body Awareness Questionnaire (BAQ)
Tijdsspanne: 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.
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Baseline
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Medewerkers en onderzoekers
Hier vindt u mensen en organisaties die betrokken zijn bij dit onderzoek.
Sponsor
Studie record data
Deze datums volgen de voortgang van het onderzoeksdossier en de samenvatting van de ingediende resultaten bij ClinicalTrials.gov. Studieverslagen en gerapporteerde resultaten worden beoordeeld door de National Library of Medicine (NLM) om er zeker van te zijn dat ze voldoen aan specifieke kwaliteitscontrolenormen voordat ze op de openbare website worden geplaatst.
Bestudeer belangrijke data
Studie start (Werkelijk)
4 augustus 2026
Primaire voltooiing (Geschat)
1 september 2026
Studie voltooiing (Geschat)
1 september 2026
Studieregistratiedata
Eerst ingediend
28 juli 2026
Eerst ingediend dat voldeed aan de QC-criteria
28 juli 2026
Eerst geplaatst (Werkelijk)
31 juli 2026
Updates van studierecords
Laatste update geplaatst (Werkelijk)
5 augustus 2026
Laatste update ingediend die voldeed aan QC-criteria
4 augustus 2026
Laatst geverifieerd
1 juli 2026
Meer informatie
Termen gerelateerd aan deze studie
Andere studie-ID-nummers
- ETurkmen0526
Informatie over medicijnen en apparaten, studiedocumenten
Bestudeert een door de Amerikaanse FDA gereguleerd geneesmiddel
Nee
Bestudeert een door de Amerikaanse FDA gereguleerd apparaatproduct
Nee
Deze informatie is zonder wijzigingen rechtstreeks van de website clinicaltrials.gov gehaald. Als u verzoeken heeft om uw onderzoeksgegevens te wijzigen, te verwijderen of bij te werken, neem dan contact op met register@clinicaltrials.gov. Zodra er een wijziging wordt doorgevoerd op clinicaltrials.gov, wordt deze ook automatisch bijgewerkt op onze website .