Dysphagia Management During COVID-19 Pandemic

Sponsor

Hacettepe University (Other)

Overall Status

Recruiting

CT.gov ID

NCT04509752

Collaborator

(none)

Enrollment

Location

4.7

Anticipated Duration (Months)

10.6

Patients Per Site Per Month

Study Details

Study Description

Brief Summary

The current study is aimed to determine the procedures applied in the dysphagia clinics during the COVID-19 pandemic period. A questionnaire consisting of 30 questions will be implemented. Each participant will be asked to answer the questions.

Condition or Disease	Intervention/Treatment	Phase
Dysphagia Covid19	Other: Survey

Detailed Description

The current study is aimed to understand the current clinical conditions and current practice regarding dysphagia management during the pandemic period/normalization period. It is a cross sectional online survey study. The first part is the survey development and testing, the second part is determination of swallowing centers and last part is survey distribution by google forms. A coordinator will be selected for each center to discuss the survey with the entire team and reply the questions.

Study Design

Study Type:

Observational

Anticipated Enrollment :

50 participants

Observational Model:

Cohort

Time Perspective:

Prospective

Official Title:

Experiences in Dysphagia Management During COVID-19 Pandemic

Actual Study Start Date :

Oct 8, 2020

Anticipated Primary Completion Date :

Feb 15, 2021

Anticipated Study Completion Date :

Feb 28, 2021

Arms and Interventions

Arm	Intervention/Treatment
Dysphagia clinicians Clinicians from swallowing centers (from all over the world)	Other: Survey An online survey will be sent to each clinic to answer the survey questions.

Arm

Intervention/Treatment

Dysphagia clinicians

Clinicians from swallowing centers (from all over the world)

Other: Survey

An online survey will be sent to each clinic to answer the survey questions.

Outcome Measures

Primary Outcome Measures

Online survey [3 months]
An online survey will be designed to understand the current clinical conditions and current practice regarding dysphagia management during the pandemic period/normalization period

Eligibility Criteria

Criteria

Ages Eligible for Study:

25 Years to 60 Years

Sexes Eligible for Study:

All

Accepts Healthy Volunteers:

Yes

Inclusion Criteria:

Working on a dysphagia clinic from all over the world

Exclusion Criteria:

Not willing to participate
Not working on a dysphagia clinic

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, 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:

NCT04509752

Other Study ID Numbers:

Dysphagia during COVID-19

First Posted:

Aug 12, 2020

Last Update Posted:

Feb 8, 2021

Last Verified:

Feb 1, 2021

Individual Participant Data (IPD) Sharing Statement:

Plan to Share IPD:

Studies a U.S. FDA-regulated Drug Product:

Studies a U.S. FDA-regulated Device Product:

Keywords provided by SELEN SEREL ARSLAN, Principal Investigator, Hacettepe University

dysphagia

COVID-19

Additional relevant MeSH terms:

COVID-19

Deglutition Disorders

Study Results

No Results Posted as of Feb 8, 2021