- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05325879
Relationship of Cervical Region Tension With Vagal Function
Investigation of the Relationship of Cervical Region Tension With Vagal Function and Gastrointestinal Symptoms
The increase in the tension of the soft tissues around a nerve restricts the movement, affects the function of the nerve, and makes the nerve vulnerable to entrapment. Even a mild nerve compression can cause entrapment and lead to neuroinflammation. It is known that inflammatory mediators amplify axonal sensitivity. Although the spontaneous discharge potential of visceral afferents is quite low under normal conditions, neuroinflammation increases the excitability of these fibers. With this mechanism, hyperalgesia may develop in sensory fibers in neuroinflammation. This may cause pathologies in the organs innervated by the relevant nerve.
The fascia and muscles of the cervical region surround the vagus nerve. There are two main fascial compartments in the cervical region. The SCM and trapezius muscle fascias join to the most superficial fascia of the deep cervical fascia and they together form these compartments. These fasciae superiorly attach to the cranium and inferiorly to the pectoral region. The vagus nerve emerges from the jugular foramen together with the 9th and 11th cranial nerves. It then continues through the carotid sheath in the cervical region. The carotid sheath is in contact with the SCM muscle. For this reason, it can be thought that SCM muscle tension or thickness may affect the carotid sheath and thus the function of the vagus nerve passing through it.
In summary, deterioration in vagus nerve activity plays a role in pathologies of the organs innervated by the vagus. Although the relationship between vagal dysfunction and gastrointestinal system symptoms is clear, the mechanisms affecting vagus nerve function have not yet been clarified. It has been reported in the literature that some maneuvers from the cervical region are also effective on the vagus nerve. Also, according to investigators' clinical experience, gastrointestinal symptoms are frequently observed in patients with increased cervical soft tissue tension. However, there are not enough studies investigating whether the cervical region soft tissue tension can affect the gastrointestinal system via the vagus nerve. Therefore, this study was planned to examine the relationship of cervical soft tissue tension with vagus nerve function and gastrointestinal symptoms in asymptomatic individuals and individuals with neck pain.
Study Overview
Status
Intervention / Treatment
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
-
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Sıhhiye
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Ankara, Sıhhiye, Turkey, 06100
- Yasemin Özel Aslıyüce
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Description
Inclusion Criteria:
- Being 18-50 of age,
- Having less than 30 body mass index,
- Being a volunteer
Exclusion Criteria:
- Having any type of malign disease,
- Being diagnosed with a systemic disease (cardiologic, gastrointestinal, rheumatological, neurological, etc.),
- Having any type of surgery within the last 6 months,
- Being diagnosed with Whiplash syndrome
- Having an unhealed fracture
- Pregnancy
- Using prescribed medicine for the gastrointestinal system
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Screening
- Allocation: Non-Randomized
- Interventional Model: Single Group Assignment
- Masking: Single
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
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Active Comparator: Asymptomatic Individuals
Individuals aged between 18-50 who volunteered to participate in the study, will form the control group.
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Neurodynamic test for vagus nerve
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Experimental: Individuals with neck pain
Individuals with neck pain aged between 18-50 who volunteered to participate in the study, will form the study group.
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Neurodynamic test for vagus nerve
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Evaluation of Vagal Function
Time Frame: 10 minutes, in one assessment session
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Vagus nerve function will be evaluated with the Vagus Neurodynamic Test (VAGUS-NDT).
Carta et al.
VAGUS-NDT, which was validated and reliable in 2020, evaluates vagal function selectively.
The test is performed with the patient in the supine position.
The test is considered positive if unpleasant sensations are described when pressure is applied to the abdomen after the head is placed in cervicocranial flexion, lateral flexion, and rotation.
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10 minutes, in one assessment session
|
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Evaluation of SCM Muscle Tension
Time Frame: 10 minutes, in one assessment session.
|
SCM muscle tension will be performed with Myoton-3 (Muomeetria AS, Tallinn, Estonia) myometer.
Myometer is a high validity and reliability method used to evaluate muscle tension.
During the measurement, the device will give the tension of the muscle numerically by making a light touch on the skin.
For the measurement, the myotone will be placed perpendicular to the midpoint between the anterior surface of the manubrium sterni and the mastoid process of the temporal bone, and an average of 10 measurements will be used.
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10 minutes, in one assessment session.
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Hospital Anxiety and Depression Scale
Time Frame: 10 minutes, in one assessment session
|
Hospital Anxiety and Depression Scale was developed by Zigmond and Snaith, and the Turkish version of the scale was published by Aydemir et al.
The scale consists of 14 items, 7 of which assess anxiety and 7 of which assess depression symptoms.
It is a 4-point Likert scale type and is scored between 0-3.
A high score indicates high levels of anxiety and depression
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10 minutes, in one assessment session
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Evaluation of Neck Disability
Time Frame: 5 minutes, in one assessment session.
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The level of neck disability will be evaluated using the The Neck Disability Questionnaire.
It was developed by Vernon et al. as a neck version of the Oswestry Low Back Pain Scale.
Within the scope of this study, the Neck Disability Questionnaire will be applied to the participants with a neck pain severity of 3 and above on the Numerical Pain Rating Scale.
The Neck Disability Questionnaire includes ten questions about pain, personal care, concentration, work, driving, and sleeping.
Each question is scored between 0-5 points.
The total score is evaluated out of 50.
A high score means a high disability.
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5 minutes, in one assessment session.
|
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Evaluation of Pain Intensity
Time Frame: 1 minutes, in one assessment session.
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Pain intensity will be assessed using the Numerical Pain Rating Scale.
The 11-item version of the scale, which is frequently used to measure the severity of pain in adults, will be used.
Within the scope of this study, a scale will be used to measure the severity of neck pain of the participants.
With this scale, participants will be asked to measure their neck pain on a scale of 0-10.
A value of '0' indicates no pain and a value of '10' indicates excruciating pain.
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1 minutes, in one assessment session.
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Evaluation of Gastrointestinal Symptoms
Time Frame: 5 minutes, in one assessment session.
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Gastrointestinal symptoms will be evaluated using the Gastrointestinal Symptoms Rating Scale.
Revicki et al.
The scale developed by CBS measures common symptoms in CBS diseases.
A seven-point Likert-type scale consisting of 15 items consisting of five sub-dimensions was made in order.
These sub-dimensions are; reflux, indigestion, diarrhea, constipation and abdominal pain.
The total score ranges from 15 to 105, with a high score indicating severe symptoms.
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5 minutes, in one assessment session.
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Collaborators and Investigators
Sponsor
Investigators
- Study Chair: Utku Berberoğlu, MSc, Hacettepe University
- Study Chair: Özgün Uysal, MSc, Hacettepe University
- Study Director: Özlem Ülger, Professor, Hacettepe University
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Estimated)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- HUSpine014
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
product manufactured in and exported from the U.S.
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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