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CompletedNCT04509752Updated Jan 3, 2024

Dysphagia Management During COVID-19 Pandemic

An observational study in Dysphagia and Covid19, sponsored by Hacettepe University. Completed at 1 site in Turkey. Open to participants aged 25 Years to 60 Years, including healthy volunteers. Per ClinicalTrials.gov, last updated 2024-01-03.

Sponsored by Hacettepe University · Observational

Study type
Observational
Model
Cohort
Time perspective
Prospective
Enrollment
23
Ages
25 Years to 60 Years
Sex
All
01

Study 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.

Read the 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.

02

Conditions studied

  • Dysphagia
  • Covid19

Keywords

  • dysphagia
  • COVID-19
03

In context

COVID-19

7,638 studies on the registry are indexed under COVID-19; 488 are open to participants now.

This study's enrollment of 23 is below the median of 260 across 3,135 observational studies indexed under COVID-19.

Browse COVID-19 studies →

Lead sponsor

Hacettepe University is the lead sponsor of 983 studies on the registry; 212 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
25 Years to 60 Years
Sexes eligible
All
Accepts healthy volunteers
Yes
Sampling method
Non-probability sample

Study population

Clinicians who work on a dysphagia clinic will be included.

Inclusion criteria

  • Working on a dysphagia clinic from all over the world

Exclusion criteria

Exclusion Criteria:

  • Not willing to participate
  • Not working on a dysphagia clinic
05

Study design

Observational model
Cohort
Time perspective
Prospective
Enrollment
23 participants (actual)
Patient registry
No

Groups and cohorts

  • Dysphagia clinicians

    Clinicians from swallowing centers (from all over the world)

    Other: Survey

Interventions

  • OtherSurvey

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

06

What researchers measure

Primary outcomes

  1. Online survey

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

    Time frame: 3 months

07

Study locations

1 site
  • Hacetttepe University
    Ankara, 06100, Turkey
08

References and documents

Individual participant data

Plan to share: No

No publications or documents are linked to this record.

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Jan 3, 2024, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT04509752
Lead sponsor
Hacettepe University
Responsible party
SELEN SEREL ARSLAN (Principal Investigator, Hacettepe University) — Principal investigator
First posted
Aug 12, 2020
Start date
Oct 8, 2020
Primary completion
Mar 15, 2021
Completion
Mar 15, 2021
Last update
Jan 3, 2024

Study contacts

SELEN SEREL ARSLAN
principal investigator · Hacettepe University

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is completed, as verified in Jan 2024. You cannot join it, but the record below documents what was studied.

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