Neurogenic Dysphagia Clinical Trial
Official title:
The Relationship Between Dysphagia Symptom Severity and Quality of Life
| Verified date | January 2024 |
| Source | Hacettepe University |
| Contact | n/a |
| Is FDA regulated | No |
| Health authority | |
| Study type | Observational |
The aim of the study is to investigate the relationship between dysphagia symptom severity and quality of life of the patients with neurogenic dysphagia.
| Status | Completed |
| Enrollment | 84 |
| Est. completion date | September 8, 2017 |
| Est. primary completion date | September 8, 2017 |
| Accepts healthy volunteers | |
| Gender | All |
| Age group | 20 Years to 65 Years |
| Eligibility | Inclusion Criteria: - Willing to participate in the study - Being over the age of 20 - Normal cognitive function - Suffering from dysphagia at least one month Exclusion Criteria: - Being under the age of 20 and above 65 years. - Abnormal cognitive function - Clinically unstable neurological disease |
| Country | Name | City | State |
|---|---|---|---|
| Turkey | Hacetttepe University | Ankara |
| Lead Sponsor | Collaborator |
|---|---|
| Hacettepe University |
Turkey,
| Type | Measure | Description | Time frame | Safety issue |
|---|---|---|---|---|
| Primary | Dysphagia symptom severity | Dysphagia symptom severity will be determined by an eating assessment tool. | 1 month | |
| Secondary | Quality of life assessment | Swallowing related quality of life will be determined by an dysphagia specific quality of life instrument called Swallow Quality of Life. | 1 month |
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