Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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COMPLETED
84 participants
OBSERVATIONAL
2017-08-08
2017-09-08
Brief Summary
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Detailed Description
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Conditions
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Study Design
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COHORT
PROSPECTIVE
Study Groups
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Neurogenic dysphagia
Patients with neurogenic dysphagia who will willing to participate in the study, being over the age of 18, normal cognitive function (\[24 points according to the Mini Mental State Examination), suffering from dysphagia at least one month, and having clinically stable neurological disease will be included. Dysphagia evaluation will be performed.
Dysphagia evaluation
Dysphagia evaluation is performed in a clinical setting by an eating assessment tool. Swallowing related quality of life is also assessed.
Interventions
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Dysphagia evaluation
Dysphagia evaluation is performed in a clinical setting by an eating assessment tool. Swallowing related quality of life is also assessed.
Eligibility Criteria
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Inclusion Criteria
* Being over the age of 20
* Normal cognitive function
* Suffering from dysphagia at least one month
Exclusion Criteria
* Abnormal cognitive function
* Clinically unstable neurological disease
20 Years
65 Years
ALL
No
Sponsors
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Hacettepe University
OTHER
Responsible Party
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SELEN SEREL ARSLAN
Principal Investigator
Principal Investigators
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SELEN SEREL ARSLAN
Role: PRINCIPAL_INVESTIGATOR
Hacettepe University
Locations
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Hacetttepe University
Ankara, , Turkey (Türkiye)
Countries
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Other Identifiers
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HACETTEPEUNIVERSITY
Identifier Type: -
Identifier Source: org_study_id
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