- ICH GCP
- Amerikanska kliniska prövningsregistret
- Klinisk prövning NCT07739836
Effects of Physical Use Characteristics During Academic Education on Musculoskeletal Function and Body Awareness in University Students From Different Academic Departments
4 augusti 2026 uppdaterad av: 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.
Studieöversikt
Status
Rekrytering
Detaljerad beskrivning
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.
Studietyp
Observationell
Inskrivning (Beräknad)
300
Kontakter och platser
Det här avsnittet innehåller kontaktuppgifter för dem som genomför studien och information om var denna studie genomförs.
Studiekontakt
- Namn: Ezgi Türkmen
- Telefonnummer: 0090 216 547 26 00
- E-post: turkmnezgi@gmail.com
Studieorter
-
-
-
Istanbul, Turkiet (Türkiye)
- Rekrytering
- Haliç Üniversitesi
-
Kontakt:
- Ayşenur Çetinkaya
- Telefonnummer: 0090 212 924 24 44
- E-post: aysenurcetinkaya@halic.edu.tr
-
-
Deltagandekriterier
Forskare letar efter personer som passar en viss beskrivning, så kallade behörighetskriterier. Några exempel på dessa kriterier är en persons allmänna hälsotillstånd eller tidigare behandlingar.
Urvalskriterier
Åldrar som är berättigade till studier
- Vuxen
Tar emot friska volontärer
Ja
Testmetod
Icke-sannolikhetsprov
Studera befolkning
Physiotherapy and Rehabilitation Department Students & Architecture Department Students
Beskrivning
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.
Studieplan
Det här avsnittet ger detaljer om studieplanen, inklusive hur studien är utformad och vad studien mäter.
Hur är studien utformad?
Designdetaljer
Kohorter och interventioner
Grupp / Kohort |
|---|
|
Group I
Physiotherapy and Rehabilitation Department Students
|
|
Group II
Architecture Department Students
|
Vad mäter studien?
Primära resultatmått
Resultatmått |
Åtgärdsbeskrivning |
Tidsram |
|---|---|---|
|
Multifidus Muscle Stabilization Assessment
Tidsram: 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
Tidsram: 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
Tidsram: 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)
Tidsram: 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
|
Samarbetspartners och utredare
Det är här du hittar personer och organisationer som är involverade i denna studie.
Sponsor
Studieavstämningsdatum
Dessa datum spårar framstegen för inlämningar av studieposter och sammanfattande resultat till ClinicalTrials.gov. Studieposter och rapporterade resultat granskas av National Library of Medicine (NLM) för att säkerställa att de uppfyller specifika kvalitetskontrollstandarder innan de publiceras på den offentliga webbplatsen.
Studera stora datum
Studiestart (Faktisk)
4 augusti 2026
Primärt slutförande (Beräknad)
1 september 2026
Avslutad studie (Beräknad)
1 september 2026
Studieregistreringsdatum
Först inskickad
28 juli 2026
Först inskickad som uppfyllde QC-kriterierna
28 juli 2026
Första postat (Faktisk)
31 juli 2026
Uppdateringar av studier
Senaste uppdatering publicerad (Faktisk)
5 augusti 2026
Senaste inskickade uppdateringen som uppfyllde QC-kriterierna
4 augusti 2026
Senast verifierad
1 juli 2026
Mer information
Termer relaterade till denna studie
Andra studie-ID-nummer
- ETurkmen0526
Läkemedels- och apparatinformation, studiedokument
Studerar en amerikansk FDA-reglerad läkemedelsprodukt
Nej
Studerar en amerikansk FDA-reglerad produktprodukt
Nej
Denna information hämtades direkt från webbplatsen clinicaltrials.gov utan några ändringar. Om du har några önskemål om att ändra, ta bort eller uppdatera dina studieuppgifter, vänligen kontakta register@clinicaltrials.gov. Så snart en ändring har implementerats på clinicaltrials.gov, kommer denna att uppdateras automatiskt även på vår webbplats .