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Dysphagia Management During COVID-19 Pandemic

The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Know the risks and potential benefits of clinical studies and talk to your health care provider before participating. Read our disclaimer for details.
 
ClinicalTrials.gov Identifier: NCT04509752
Recruitment Status : Not yet recruiting
First Posted : August 12, 2020
Last Update Posted : August 12, 2020
Sponsor:
Information provided by (Responsible Party):
SELEN SEREL ARSLAN, Hacettepe University

Tracking Information
First Submitted Date August 11, 2020
First Posted Date August 12, 2020
Last Update Posted Date August 12, 2020
Estimated Study Start Date August 20, 2020
Estimated Primary Completion Date November 15, 2020   (Final data collection date for primary outcome measure)
Current Primary Outcome Measures
 (submitted: August 11, 2020)
Online survey [ Time Frame: 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
Original Primary Outcome Measures Same as current
Change History No Changes Posted
Current Secondary Outcome Measures Not Provided
Original Secondary Outcome Measures Not Provided
Current Other Pre-specified Outcome Measures Not Provided
Original Other Pre-specified Outcome Measures Not Provided
 
Descriptive Information
Brief Title Dysphagia Management During COVID-19 Pandemic
Official Title Experiences in Dysphagia Management During COVID-19 Pandemic
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.
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 Type Observational
Study Design Observational Model: Cohort
Time Perspective: Prospective
Target Follow-Up Duration Not Provided
Biospecimen Not Provided
Sampling Method Non-Probability Sample
Study Population Clinicians who work on a dysphagia clinic will be included.
Condition
  • Dysphagia
  • Covid19
Intervention Other: Survey
An online survey will be sent to each clinic to answer the survey questions.
Study Groups/Cohorts Dysphagia clinicians
Clinicians from swallowing centers (from all over the world)
Intervention: Other: Survey
Publications * Not Provided

*   Includes publications given by the data provider as well as publications identified by ClinicalTrials.gov Identifier (NCT Number) in Medline.
 
Recruitment Information
Recruitment Status Not yet recruiting
Estimated Enrollment
 (submitted: August 11, 2020)
50
Original Estimated Enrollment Same as current
Estimated Study Completion Date November 30, 2020
Estimated Primary Completion Date November 15, 2020   (Final data collection date for primary outcome measure)
Eligibility Criteria

Inclusion Criteria:

  • Working on a dysphagia clinic from all over the world

Exclusion Criteria:

  • Not willing to participate
  • Not working on a dysphagia clinic
Sex/Gender
Sexes Eligible for Study: All
Ages 25 Years to 60 Years   (Adult)
Accepts Healthy Volunteers Yes
Contacts
Contact: SELEN SEREL ARSLAN +905356643007 selen.serel@hacettepe.edu.tr
Contact: NUMAN DEMİR +905424848079 numan@hacettepe.edu.tr
Listed Location Countries Turkey
Removed Location Countries  
 
Administrative Information
NCT Number NCT04509752
Other Study ID Numbers Dysphagia during COVID-19
Has Data Monitoring Committee No
U.S. FDA-regulated Product
Studies a U.S. FDA-regulated Drug Product: No
Studies a U.S. FDA-regulated Device Product: No
IPD Sharing Statement
Plan to Share IPD: No
Responsible Party SELEN SEREL ARSLAN, Hacettepe University
Study Sponsor Hacettepe University
Collaborators Not Provided
Investigators
Principal Investigator: SELEN SEREL ARSLAN Hacettepe University
PRS Account Hacettepe University
Verification Date August 2020