The Turkish Feeding/Swallowing Impact Survey

Sponsor

Hacettepe University (Other)

Overall Status

Completed

CT.gov ID

NCT03005093

Collaborator

(none)

117

Enrollment

Location

3.9

Actual Duration (Months)

29.7

Patients Per Site Per Month

Study Details

Study Description

Brief Summary

The purpose of this study is to test the reliability and validity of the Turkish Feeding/Swallowing Impact Survey among caregivers of pediatric patients with swallowing disorders.

Condition or Disease	Intervention/Treatment	Phase
Deglutition Disorder Dysphagia Outcome Assessment Quality of Life	Other: CAREGIVERS Other: CHILDREN OF CAREGIVERS

Detailed Description

The purpose of this study is to test the reliability and validity of the Turkish Feeding/Swallowing Impact Survey among caregivers of pediatric patients with swallowing disorders.The internal consistency, test-retest reliability, and criterion validity of T-EAT-10 will be investigated. The internal consistency will be assessed using Cronbach's alpha. Intraclass correlation coefficient (ICC) value with 95 % confidence intervals will be calculated for test-retest reliability. The criterion validity of the scale will be determined by assessing the correlation between the Turkish Feeding/Swallowing Impact Survey and Karaduman Chewing Performance Scale, Tongue Thrust Rating Scale, Pediatric version of the Eating Assessment Tool. The validity will also be determined by completion of the Turkish Feeding/Swallowing Impact Survey before and after swallowing rehabilitation of pediatric patients.

Study Design

Study Type:

Observational

Actual Enrollment :

117 participants

Observational Model:

Cohort

Time Perspective:

Prospective

Official Title:

Reliability and Validity of the Turkish Feeding/Swallowing Impact Survey

Actual Study Start Date :

Jan 15, 2017

Actual Primary Completion Date :

May 15, 2017

Actual Study Completion Date :

May 15, 2017

Arms and Interventions

Arm	Intervention/Treatment
CAREGIVERS Caregivers of pediatric patients with swallowing disorders will be recruited.	Other: CAREGIVERS The Turkish Feeding/Swallowing Impact Survey will be completed by the caregivers
CHILDREN OF CAREGIVERS Pediatric patients with swallowing disorders will be recruited.	Other: CHILDREN OF CAREGIVERS Chewing performance with Karaduman Chewing Performance Scale, tongue control with Tongue Thrust Rating Scale, dysphagia symptom severity with the Pediatric version of the Eating Assessment Tool will be evaluated. These assessments will be done before and after swallowing rehabilitation program.

Arm

Intervention/Treatment

CAREGIVERS

Caregivers of pediatric patients with swallowing disorders will be recruited.

Other: CAREGIVERS

The Turkish Feeding/Swallowing Impact Survey will be completed by the caregivers

CHILDREN OF CAREGIVERS

Pediatric patients with swallowing disorders will be recruited.

Other: CHILDREN OF CAREGIVERS

Chewing performance with Karaduman Chewing Performance Scale, tongue control with Tongue Thrust Rating Scale, dysphagia symptom severity with the Pediatric version of the Eating Assessment Tool will be evaluated. These assessments will be done before and after swallowing rehabilitation program.

Outcome Measures

Primary Outcome Measures

The Turkish Feeding/Swallowing Impact Survey [6 months]
This scale is used to determine the concerns of caregivers related to their children feeding/swallowing difficulties

Secondary Outcome Measures

The Karaduman Chewing Performance Scale [6 months]
This scale is used to determine chewing performance level of children
Tongue Thrust Rating Scale [6 months]
This scale is used to determine tongue thrust severity of children
Pediatric version of the Eating Assessment Tool [6 months]
This tool is used to determine initial dysphagia symptom severity of children

Eligibility Criteria

Criteria

Ages Eligible for Study:

20 Years to 65 Years

Sexes Eligible for Study:

All

Accepts Healthy Volunteers:

Yes

Inclusion Criteria:

Having a child with swallowing disorders aged between 6 months-18 years

Exclusion Criteria:

Having a child without swallowing disorders
Having a child with swallowing disorders aged below 6 months

Contacts and Locations

Locations

	Site	City	State	Country	Postal Code
1	Hacetttepe University	Ankara		Turkey	06100

Sponsors and Collaborators

Hacettepe University

Investigators

Principal Investigator: SELEN SEREL ARSLAN, PhD, Hacettepe University

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.

Responsible Party:

SELEN SEREL ARSLAN, Principal Investigator, Hacettepe University

ClinicalTrials.gov Identifier:

NCT03005093

Other Study ID Numbers:

HACETTEPE UNI

First Posted:

Dec 29, 2016

Last Update Posted:

Aug 17, 2017

Last Verified:

Aug 1, 2017

Individual Participant Data (IPD) Sharing Statement:

Plan to Share IPD:

Additional relevant MeSH terms:

Deglutition Disorders

Study Results

No Results Posted as of Aug 17, 2017