Validity and Reliability of the Turkish Translation of the Yale Pharyngeal Residue Severity Rating Scale

Sponsor
Prof. Dr. Cemil Tascıoglu Education and Research Hospital Organization (Other)
Overall Status
Completed
CT.gov ID
NCT04477174
Collaborator
(none)
24
1
2
11.8

Study Details

Study Description

Brief Summary

Purpose of the study is the validity and reliability of the Turkish version of the Yale Pharyngeal Residue Severity Rating Scale (YPRSRS-T), so that it would be used as an assessment tool for dysphagia patients.

Condition or Disease Intervention/Treatment Phase

    Detailed Description

    The swallow function is a multidirectional process that depends on complex neuro-muscular network. The function can be evaluated using instrumental, such as fibreoptic endoscopic evaluation of swallowing (FEES), videofluoroscopy, or well structured scales. There are many questionnaire and scales for assessment of swallow but very few have been validated. The study will assess the construct validity and reliability of the Turkish version of Pharyngeal Residue Severity Rating Scale as known as Yale Pharyngeal Residue Severity Rating Scale.

    Study Design

    Study Type:
    Observational
    Actual Enrollment :
    24 participants
    Observational Model:
    Other
    Time Perspective:
    Prospective
    Official Title:
    Validity and Reliability of the Turkish Translation of the Yale Pharyngeal Residue Severity Rating Scale (YPRSRS-T)
    Actual Study Start Date :
    Jul 15, 2020
    Actual Primary Completion Date :
    Sep 15, 2020
    Actual Study Completion Date :
    Sep 15, 2020

    Arms and Interventions

    Arm Intervention/Treatment
    Group A

    Twelve health professionals randomised assign to as equally count. The participants match between the images with scale scores. After 2 weeks, the participants match again.

    Group B

    Twelve health professionals randomised assign to as equally count. The participants match between the images with scale scores.

    Outcome Measures

    Primary Outcome Measures

    1. Validation of Pharyngeal Residue Severity Rating Scale [2 months]

      To match between Fiberoptic Endoscopic Evaluation of Swallowing Images with Yale Pharyngeal Residue Severity Rating Scale Scores by health professionals. High match scores give high reliability, low match scores give low reliability. Match scores were compared and evaluated as statistically. High match score is better, low score is worse.

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    18 Years to 70 Years
    Sexes Eligible for Study:
    All
    Accepts Healthy Volunteers:
    Yes
    Inclusion Criteria:
    • 18-70 years

    • at least having undergraduate education on health profession

    • agree to participant

    Exclusion Criteria:
    • out of age 18-70 years

    • out of having undergraduate education

    • mental disorder

    • cognitive limitations

    • visual limitations

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 Prof Dr Cemil Tascioglu City Hospital Istanbul Turkey 34384

    Sponsors and Collaborators

    • Prof. Dr. Cemil Tascıoglu Education and Research Hospital Organization

    Investigators

    • Principal Investigator: Melis Ece Arkan Ararat, MD, University of Health Sciences, Prof Dr Cemil Tascioglu City Hospital
    • Principal Investigator: Ugur Uygan, MD, University of Health Sciences, Prof Dr Cemil Tascioglu City Hospital

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    None provided.
    Responsible Party:
    Yavuz Atar, Associate Professor, M.D., Prof. Dr. Cemil Tascıoglu Education and Research Hospital Organization
    ClinicalTrials.gov Identifier:
    NCT04477174
    Other Study ID Numbers:
    • 308
    First Posted:
    Jul 20, 2020
    Last Update Posted:
    Dec 29, 2020
    Last Verified:
    Dec 1, 2020
    Individual Participant Data (IPD) Sharing Statement:
    No
    Plan to Share IPD:
    No
    Studies a U.S. FDA-regulated Drug Product:
    No
    Studies a U.S. FDA-regulated Device Product:
    No
    Keywords provided by Yavuz Atar, Associate Professor, M.D., Prof. Dr. Cemil Tascıoglu Education and Research Hospital Organization
    Additional relevant MeSH terms:

    Study Results

    No Results Posted as of Dec 29, 2020