Turkish of the SARS-CoV-2 Anxiety Scale

December 22, 2020 updated by: DILEK SAYIK

Turkish Validity And Reliability of the SARS-CoV-2 Anxiety Scale

The coronavirus outbreak has adversely affected individuals in the community, as in the rest of the world. However, in order to carry out this epidemic period in a healthy and conscious manner, determining the anxiety levels of individuals in the society and supporting them psychologically is of great importance. In order to achieve this, healthcare professionals working clinically or academically have important duties. This study was planned to test its validity and reliability in order to adapt the Coronavirus Anxiety Scale to Turkish.

Study Overview

Status

Unknown

Intervention / Treatment

Detailed Description

Coronaviruses can be seen in animals and humans as infections that can be mild and severe in society. The SARS-CoV-2 virus, a type of coronavirus, started in China in December 2019 and has spread worldwide as of January 2020. The absence of vaccine and treatment for SARS-CoV-2 disease threatens health worldwide and significantly affects people's daily routine. In China, where the pandemic started, shopping malls and schools were closed for a while, and city entrances and exits were stopped for a while. Although there are similar practices in excellence, as in many countries, measures such as curfew, nursery and school closure continue to be taken for under-20s and over-65s. . The coronavirus epidemic that affects our entire life is not fully known about the disease process, WHO is defined as the pandemic of the epidemic, the nearest contact is the greatest risk of transmission, and the loss of many lives during this process affects all individuals in the society negatively and increases the level of anxiety .

It is a psychological reaction involving many emotions such as anxiety, stress, or anxiety, fear and distress that arise in a situation that threatens the safety of the individual. Conditions such as uncertainty, various diseases (cancer, epidemic, etc.) and losing a relative can cause anxiety. Outbreaks that occur suddenly and are at risk of death are among these reasons.

Study Type

Interventional

Enrollment (Anticipated)

300

Phase

  • Not Applicable

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

      • Eskisehir, Turkey
        • Recruiting
        • Eskisehir Osmangazi University
        • Contact:
          • AYFER AÇIKGÖZ
          • Phone Number: 05352919374

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

18 years to 60 years (Adult)

Accepts Healthy Volunteers

Yes

Genders Eligible for Study

All

Description

inclusion criteria;

  • individuals agree to participate in the study
  • 18 years old,
  • Lack of visual obstacle,
  • Knowing how to speak, read and write in Turkish.

Exclusion criteria;

  • individuals refuse to participate in the study
  • 18 years old,
  • Visually impaired,
  • Does not know how to speak, read and write in Turkish

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Primary Purpose: Other
  • Allocation: N/A
  • Interventional Model: Single Group Assignment
  • Masking: None (Open Label)

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Other: volunteer group
Only volunteer participants will be included in the research. Survey forms will be sent to individuals online. Individuals who agree to participate in the study will fill in the questionnaire and send it back online.
Survey forms will be sent to individuals online. Information about the study will be given to individuals with the informative text at the beginning of the questionnaire form. Individuals who agree to participate in the study will fill in the questionnaire and send it back online.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Anxiety in SARS-CoV-2
Time Frame: 4 weeks
anxiety increase in SARS-CoV-2 in humans.
4 weeks
Ratio of SARS-CoV-2 anxiety scale to beck anxiety scale
Time Frame: 4 weeks
The ratio of SARS-CoV-2 anxiety scale to beck anxiety scale is similar.
4 weeks

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Sponsor

Investigators

  • Principal Investigator: DILEK SAYIK, Eskisehir Osmangazi Universty

Publications and helpful links

The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

July 24, 2020

Primary Completion (Anticipated)

March 24, 2021

Study Completion (Anticipated)

April 24, 2021

Study Registration Dates

First Submitted

July 25, 2020

First Submitted That Met QC Criteria

July 28, 2020

First Posted (Actual)

July 29, 2020

Study Record Updates

Last Update Posted (Actual)

December 23, 2020

Last Update Submitted That Met QC Criteria

December 22, 2020

Last Verified

December 1, 2020

More Information

Terms related to this study

Other Study ID Numbers

  • DSAYIK2
  • Ayfer AÇIKGÖZ (Other Identifier: ESKİŞEHİR OSMANGAZİ ÜNİVERSİTESİ)
  • ERTUĞRUL ÇOLAK (Other Identifier: ESKİŞEHİR OSMANGAZİ ÜNİVERSİTESİ)
  • DENİZ YİĞİT (Other Identifier: ESKİŞEHİR OSMANGAZİ ÜNİVERSİTESİ)
  • ÖZLEM MUMCU (Other Identifier: ESKİŞEHİR ŞEHİR HASTANESİ)

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

YES

IPD Plan Description

It is planned to be published in the journal after the study is completed. The study will be shared with other researchers after it is published in the journal.

IPD Sharing Time Frame

will be shared after the work is finished.

IPD Sharing Access Criteria

It will be shared with researchers who want to use the anxiety scale.

IPD Sharing Supporting Information Type

  • STUDY_PROTOCOL

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

Clinical Trials on Anxiety

Clinical Trials on survey work

Subscribe