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Clinical Trials/NCT03241615
NCT03241615
Completed
Not Applicable

The Relationship Between Dysphagia Symptom Severity and Quality of Life

Hacettepe University1 site in 1 country84 target enrollmentAugust 8, 2017
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ConditionsNeurogenic Dysphagia

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Neurogenic Dysphagia
Sponsor
Hacettepe University
Enrollment
84
Locations
1
Primary Endpoint
Dysphagia symptom severity
Status
Completed
Last Updated
2 years ago
OverviewInvestigatorsEligibility CriteriaOutcomesSitesSimilar Trials

Overview

Brief 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.

Detailed 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.

Registry
clinicaltrials.gov
Start Date
August 8, 2017
End Date
September 8, 2017
Last Updated
2 years ago
Study Type
Observational
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

SELEN SEREL ARSLAN

Principal Investigator

Hacettepe University

Eligibility Criteria

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

Outcomes

Primary Outcomes

Dysphagia symptom severity

Time Frame: 1 month

Dysphagia symptom severity will be determined by an eating assessment tool.

Secondary Outcomes

  • Quality of life assessment(1 month)

Study Sites (1)

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