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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT03241615
Other study ID # HACETTEPEUNIVERSITY
Secondary ID
Status Completed
Phase
First received
Last updated
Start date August 8, 2017
Est. completion date September 8, 2017

Study information

Verified date January 2024
Source Hacettepe University
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

The aim of the study is to investigate the relationship between dysphagia symptom severity and quality of life of the patients with neurogenic dysphagia.


Description:

The dysphagia related quality of life and perceived dysphagia symptom severity by patients will be used as a complementary information on oropharyngeal dysphagia. Thus, the aim of the study is to investigate the relationship between dysphagia symptom severity and quality of life of the patients with neurogenic dysphagia.


Recruitment information / eligibility

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

Study Design


Related Conditions & MeSH terms


Intervention

Other:
Dysphagia evaluation
Dysphagia evaluation is performed in a clinical setting by an eating assessment tool. Swallowing related quality of life is also assessed.

Locations

Country Name City State
Turkey Hacetttepe University Ankara

Sponsors (1)

Lead Sponsor Collaborator
Hacettepe University

Country where clinical trial is conducted

Turkey, 

Outcome

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
See also
  Status Clinical Trial Phase
Completed NCT03037762 - Findings and Side-effects of Flexible Endoscopic Evaluation of Swallowing - the FEES-Registry
Terminated NCT02493491 - Neurogenic Dysphonia/Dysphagia Registry N/A
Completed NCT01995929 - Functional Endoscopy in Neurogenic Dysphagia
Recruiting NCT05190718 - Register Study: Implementation of Pharyngeal Electrostimulation Therapy for the Treatment of Acute Neurogenic Dysphagia
Completed NCT05782790 - Action Observation Therapy Program in Patients With Neurogenic Dysphagia N/A