Myotonometer Analyses of Muscles in Multiple Sclerosis Patients With Dysphagia
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ClinicalTrials.gov Identifier: NCT04369092 |
Recruitment Status :
Completed
First Posted : April 30, 2020
Last Update Posted : April 30, 2020
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Condition or disease | Intervention/treatment | Phase |
---|---|---|
Multiple Sclerosis Dysphagia Swallowing Disorder Deglutition Disorders Muscle Tonus | Other: DYMUS | Not Applicable |
Study Type : | Interventional (Clinical Trial) |
Actual Enrollment : | 28 participants |
Allocation: | Randomized |
Intervention Model: | Parallel Assignment |
Masking: | None (Open Label) |
Primary Purpose: | Other |
Official Title: | Myotonometric Assessment of Muscles in Multiple Sclerosis Patients With Dysphagia |
Actual Study Start Date : | October 2, 2019 |
Actual Primary Completion Date : | December 28, 2019 |
Actual Study Completion Date : | January 30, 2020 |

Arm | Intervention/treatment |
---|---|
without swallowing problem
patients without swallowing problem
|
Other: DYMUS
DYsphagia in MUltiple Sclerosis (DYMUS) that was questionnare and Eating Assessment Tool (EAT-10) were used for assess swallowing problem. All individuals were classified according to DYMUS. The DYMUS Score was 1 or 2 was taken as mild swallowing problems, 3 or more was taken as severe swallowing problems. Patients were divided into three groups; first group that include patients without swallowing problems, second group that include patients with mild swallowing problems, third group that include severe swallowing problems.
Other Name: evaluating oropharyngeal dysphagia |
mild swallowing problem
patients with mild swallowing problem
|
Other: DYMUS
DYsphagia in MUltiple Sclerosis (DYMUS) that was questionnare and Eating Assessment Tool (EAT-10) were used for assess swallowing problem. All individuals were classified according to DYMUS. The DYMUS Score was 1 or 2 was taken as mild swallowing problems, 3 or more was taken as severe swallowing problems. Patients were divided into three groups; first group that include patients without swallowing problems, second group that include patients with mild swallowing problems, third group that include severe swallowing problems.
Other Name: evaluating oropharyngeal dysphagia |
severe swallowing problem
patients with severe swallowing problem
|
Other: DYMUS
DYsphagia in MUltiple Sclerosis (DYMUS) that was questionnare and Eating Assessment Tool (EAT-10) were used for assess swallowing problem. All individuals were classified according to DYMUS. The DYMUS Score was 1 or 2 was taken as mild swallowing problems, 3 or more was taken as severe swallowing problems. Patients were divided into three groups; first group that include patients without swallowing problems, second group that include patients with mild swallowing problems, third group that include severe swallowing problems.
Other Name: evaluating oropharyngeal dysphagia |
- Myotonometric Measurement [ Time Frame: through study completion, average one hour ]MyotonPro® device was used to measure muscles' viscoelastic parameters. The device is valid and reliable for measuring viscoelastic parameters (5, 6). Tonus, stiffness, elasticity of the muscles were recorded. Three measurements were bilaterally taken for each muscle. For each muscle, the average values of stiffness, tone and elasticity were retained as the main MyotonPRO outcomes. Myotonometric measurements were carried out for Masseter, Orbicularis Oris and Sternocleidomastoid (SKM) in supine position.
- Eating Assessment Tool [ Time Frame: through study completion, average one hour ]Eating Assessment Tool was used to assess symptom of dysphagia. EAT-10 consisted of ten items, each of items was scored from 0 to 4. As the score increases, the patient's symptoms become deterioration.

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Ages Eligible for Study: | 18 Years and older (Adult, Older Adult) |
Sexes Eligible for Study: | All |
Accepts Healthy Volunteers: | No |
Inclusion Criteria:
- being diagnosed with Mc Donald's Multiple sclerosis (MS) in accordance with 2010 criteria,
- being between the ages of 18-45.
Exclusion Criteria:
- having psychological, orthopedic and other neurological disorders,
- pregnancy,
- having had an attack in the last 3 months,
- application of botulinum toxin in the last 6 months.

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.
Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT04369092
Turkey | |
Hasan Kalyoncu University | |
Gaziantep, Turkey |
Responsible Party: | Tuba Maden, Principal Investigator, clinical research, Hasan Kalyoncu University |
ClinicalTrials.gov Identifier: | NCT04369092 |
Other Study ID Numbers: |
2019/105 |
First Posted: | April 30, 2020 Key Record Dates |
Last Update Posted: | April 30, 2020 |
Last Verified: | April 2020 |
Studies a U.S. FDA-regulated Drug Product: | No |
Studies a U.S. FDA-regulated Device Product: | No |
Deglutition Disorders Multiple Sclerosis Disease Sclerosis Pathologic Processes Demyelinating Autoimmune Diseases, CNS Autoimmune Diseases of the Nervous System Nervous System Diseases |
Demyelinating Diseases Autoimmune Diseases Immune System Diseases Esophageal Diseases Gastrointestinal Diseases Digestive System Diseases Pharyngeal Diseases Otorhinolaryngologic Diseases |