- ICH GCP
- Amerikanska kliniska prövningsregistret
- Klinisk prövning NCT03856008
Effect of Cervical Spinal Stabilization Exercise Programs by Magnetic Resonance Imaging in Healthy Individuals
17 juni 2019 uppdaterad av: Erdi Kayabınar, Hacettepe University
Investigation of Morphological Changes of Cervical Spinal Stabilization Exercise Programs Focused on Flexor and Extensor Muscles in Cervical Muscles by Magnetic Resonance Imaging in Healthy Individuals
The aim of this study was to investigate the morphological changes in the neck muscles of cervical spinal stabilization exercises focused on flexor and extensor muscles applied to healthy individuals.
Studieöversikt
Status
Avslutad
Betingelser
Intervention / Behandling
Detaljerad beskrivning
In the prevention and treatment of cervical region pathologies, various exercise methods are applied in the clinic.
The clinical exercises vary according to the time and severity of the pathology but also according to the pathology itself.
These exercises include exercises focusing on flexor or extensor muscles.
The aim of this study was to investigate the morphological changes in the neck muscles of cervical spinal stabilization exercises focused on flexor and extensor muscles applied to healthy individuals.
At least 27 healthy male subjects between the age of 18-30 are planned to be included in the study.
Individuals will be divided into 3 groups by simple randomization method.
In one group cervical stabilization exercise program focused on the flexor muscles will be applied and the other group cervical stabilization exercise program focused on the extensor muscles will be applied for 8 weeks.
Individuals in the control group will only be evaluated without exercise.
In the study, by using magnetic resonance imaging (MRI) method as the main evaluation, muscle anatomical cross-sectional area and T2 relaxation time measurements will be made and morphological changes in muscles will be determined.
These evaluation procedures will be performed on longus colli, sternocleidomastoid, semispinalis cervicis, multifidus and upper trapezius muscles.
As additional evaluation methods, muscle strength and muscle endurance tests, normal joint motion measurements, posture evaluation and MRI measurement of cervical spine curvature will be performed.
All evaluations will be performed at the beginning and at the end of these 8 weeks and the effects of the exercises applied on the muscles in the two groups will be examined.
Studietyp
Interventionell
Inskrivning (Faktisk)
27
Fas
- Inte tillämpbar
Kontakter och platser
Det här avsnittet innehåller kontaktuppgifter för dem som genomför studien och information om var denna studie genomförs.
Studieorter
-
-
Sıhhıye
-
Ankara, Sıhhıye, Kalkon, 06430
- Hacettepe University Faculty of Physical Therapy and Rehabilitation
-
-
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
18 år till 30 år (Vuxen)
Tar emot friska volontärer
Nej
Kön som är behöriga för studier
Manlig
Beskrivning
Inclusion Criteria:
- being healthy
- age between 18 to 30 years
- agree to participate in the study
Exclusion Criteria:
- to undergo any surgical procedure of the vertebral column
- inflammatory disease
- rheumatological disease
- history of malignancy
- congenital spinal cord anomaly
- congenital and/or spinal deformities
- radiculopathy
- myelopathy
- other neurological disorders
- vestibular disorders and/or trauma history
Studieplan
Det här avsnittet ger detaljer om studieplanen, inklusive hur studien är utformad och vad studien mäter.
Hur är studien utformad?
Designdetaljer
- Primärt syfte: Behandling
- Tilldelning: Randomiserad
- Interventionsmodell: Parallellt uppdrag
- Maskning: Dubbel
Vapen och interventioner
Deltagargrupp / Arm |
Intervention / Behandling |
---|---|
Experimentell: Exercises focused on flexor muscles.
Flexor cervical stabilization exercises will be applied.
|
Exercises emphasis flexor muscles.
|
Experimentell: Exercises focused on extensor muscles.
Extensor cervical stabilization exercises will be applied.
|
Exercises emphasis extensor muscles.
|
Inget ingripande: Control.
No intervention will be applied.
|
Vad mäter studien?
Primära resultatmått
Resultatmått |
Åtgärdsbeskrivning |
Tidsram |
---|---|---|
Cervical muscles cross sectional area
Tidsram: Change from baseline time at the end of 8 week
|
Measurement of the cross-sectional area of the examined muscles by axial mri images.
The circles of the muscles will be drawn by hand and examined with a computer program.
|
Change from baseline time at the end of 8 week
|
Cervical muscle T2 relaxation time
Tidsram: change from baseline time at the end of 8 week
|
T2 relaxation time of circled muscles will be measured with milliseconds.
T2 axial and t2 mapping images will be obtained with mri.
|
change from baseline time at the end of 8 week
|
Sekundära resultatmått
Resultatmått |
Åtgärdsbeskrivning |
Tidsram |
---|---|---|
Cervical muscle strength
Tidsram: change from baseline score at the end of 8 week
|
The strength of the cervical flexor and extensor muscles and deltoid muscles will be measured by a digital hand dynamometer (Lafayette Instrument Company, USA).
The measurements of the dynamometer will be based on fine muscle test positions described by Lovett.
When measuring the muscle strength, resistance will be given from the frontal region for flexors and over the occipital region for the cervical extensors.
Resistance for deltoid muscles will be given around the shoulder.
The tests will be repeated three times and the highest of 3 repeated results obtained from these measurements will be recorded.
The strength of the muscles around the scapula will be evaluated with manual muscle test, which is rated at 0-5 points developed by Lovett.
5 point is maximum and 0 is the minimum point.
Statistical analyzes will be done with total muscle strength values.
A total of eight muscle muscle tests will be performed to evaluate the scapular muscles.
|
change from baseline score at the end of 8 week
|
New York posture rating chart
Tidsram: change from baseline score at the end of 8 week
|
This evaluation system is scored by monitoring the posture changes that may occur in 13 different parts of the body.
Accordingly, if the person's posture is correct five points will be given.If impairment is moderate, three points will be given and if the impairment is severe, 0 point will be given.
|
change from baseline score at the end of 8 week
|
Tragus angle measurement
Tidsram: change from baseline score at the end of 8 week
|
The evaluation of the tragus angle will be used as a result of the evaluation of the photograph taken in front of the checkered back surface with the computer program.
The Tragus, ear and C7 vertebrae will be marked and measured.
|
change from baseline score at the end of 8 week
|
Cervical flexor and extensor endurance test
Tidsram: change from baseline score at the end of 8 week
|
The endurance evaluation of the deep cervical flexor muscles patients will be lied in the supine position, while the hands are in the free position on the abdomen, and the patient will be asked to remove the head slightly with the instruction.
A slight amount (30%) craniocervical flexion will be required after this position has been taught to the patient.
The time in which the patient maintains the position while maintaining the craniocervical flexion will be recorded in seconds.
In the evaluation of endurance of deep cervical extensor muscles, the individual will be asked to lie down from T6 level and the head and neck will droop from the bed.
The person will be instructed to bear the weight (4 kg in men) attached to a velcro placed over the ears in this position.
The test will begin with a slight amount of craniocervical flexion, as if the individual makes head up against weight, and the time the individual maintains this position will be measured in seconds.
|
change from baseline score at the end of 8 week
|
Cervical range of motion measurement
Tidsram: change from baseline score at the end of 8 week
|
The Cervical Range of Motion (Performance Attainment Associates, St. Paul, MN, 55117, United States) (CROM 3) device will be used for the active evaluation of cervical range of motion.
Flexion-extension, rotation and lateral flexion measurements will be performed at appropriate positions.
The value found on the compass of the device will be recorded after each measurement.
|
change from baseline score at the end of 8 week
|
Evaluation of cervical spine curvature
Tidsram: change from baseline score at the end of 8 week
|
In the evaluation of cervical spine curvature, measurements of Cobb angle will be used on images taken in sagittal plane with MRI.
|
change from baseline score at the end of 8 week
|
Samarbetspartners och utredare
Det är här du hittar personer och organisationer som är involverade i denna studie.
Sponsor
Utredare
- Huvudutredare: Erdi Kayabınar, MSc, Hacettepe University
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)
25 februari 2019
Primärt slutförande (Faktisk)
2 maj 2019
Avslutad studie (Faktisk)
17 juni 2019
Studieregistreringsdatum
Först inskickad
25 februari 2019
Först inskickad som uppfyllde QC-kriterierna
25 februari 2019
Första postat (Faktisk)
27 februari 2019
Uppdateringar av studier
Senaste uppdatering publicerad (Faktisk)
18 juni 2019
Senaste inskickade uppdateringen som uppfyllde QC-kriterierna
17 juni 2019
Senast verifierad
1 juni 2019
Mer information
Termer relaterade till denna studie
Andra studie-ID-nummer
- KA-180136
Plan för individuella deltagardata (IPD)
Planerar du att dela individuella deltagardata (IPD)?
Nej
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 .
Kliniska prövningar på Friska
-
University of MiamiJames and Esther King Biomedical Research ProgramAvslutadHealthy Lifetime Icke-rökareFörenta staterna
-
University of LeicesterNational Institute for Health Research, United KingdomAvslutadPatienter med hjärtsvikt och konserverad ejektionsfraktion - HFpEF | Patienter med hjärtsvikt med reducerad ejektionsfraktion - HFrEF | Healthy Controls Group - ålders- och könsmatchad
-
University Hospital, GrenobleUniversity Hospital, Clermont-Ferrand; Grenoble Institut des NeurosciencesAvslutadParkinsons sjukdom | Healthy Controls Group - ålders- och könsmatchadFrankrike