Burnout, Covid 19, Smarthphone Addiction

February 18, 2022 updated by: Kutahya Health Sciences University

Assessment of Burnout Syndrome and Smartphone Addiction in Healthcare Workers Actively Working During the COVID-19 Pandemic

We investigate burnout syndrome and smartphone addiction in healthcare workers, including doctors, nurses, medical secretaries, security guards, and cleaning staff, who have been actively working from the beginning of the COVID-19 pandemic. target population included 1190 healthcare workers, from which a total of 183 agreed to participate in the study and met the inclusion criteria for participation. A sociodemographic data form, the Maslach Burnout Inventory, and the Smartphone Addiction Scale-Short Version were used as the data collection tools.

Study Overview

Status

Completed

Intervention / Treatment

Detailed Description

Significant differences in burnout syndrome were found in doctors and nurses. A relationship was observed between emotional burnout (EB), desensitization, and smartphone addiction, as well as between doctor and nurse group, and smartphone addiction. According to the linear regression analysis, it was determined that 17% of the change in the smartphone addiction score was related to age and 16% to master education level.Doctors and nurses experience the highest rate of burnout syndrome and smartphone addiction, and EB and desensitization were more likely to have smartphone addiction. Age and high education can affect smarthphone addiction

Study Type

Interventional

Enrollment (Actual)

183

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

    • None Selected
      • Rize, None Selected, Turkey, 53100
        • Recep Tayyip Erdoğan University

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

  • Child
  • Adult
  • Older Adult

Accepts Healthy Volunteers

No

Genders Eligible for Study

All

Description

Inclusion Criteria:

  1. Being older than 18 years of age
  2. Working as medical staff
  3. Having no systemic or psychiatric disorders
  4. No psychotropic substances use
  5. No alcohol or substance use

Exclusion Criteria:

-

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: Health Services Research
  • Allocation: N/A
  • Interventional Model: Single Group Assignment
  • Masking: None (Open Label)

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Other: healthcare workers
doctors, nurses, medical secretaries, security guards, and cleaning staff
healthcare

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
maslach burnout scale
Time Frame: 30 minutes
This tool was developed by Maslach and Jackson (1981), and the validity and reliability study of its Turkish version was conducted by Ergin (1992). The inventory has 22 items, which are scored on a 5-point Likert-type scale with anchors of 0 (never) and 4 (always). The MBI has three subscales: emotional burnout (9 items), desensitization (5 items), and low personal success (8 items
30 minutes

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
smarthphone addiction scale
Time Frame: 15 minutes
This 6-point Likert-type scale was developed by Kwon et al. to assess the risk of smartphone addiction. Total scale scores range from 10 to 60, with higher scores indicating higher risk of addiction. This is a single factor scale, and it has no subscales. The Cronbach's alpha coefficient of internal consistency and concurrent validity was 0.91 for the original scale
15 minutes

Collaborators and Investigators

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

February 25, 2021

Primary Completion (Actual)

June 30, 2021

Study Completion (Actual)

October 27, 2021

Study Registration Dates

First Submitted

February 18, 2022

First Submitted That Met QC Criteria

February 18, 2022

First Posted (Actual)

February 21, 2022

Study Record Updates

Last Update Posted (Actual)

February 21, 2022

Last Update Submitted That Met QC Criteria

February 18, 2022

Last Verified

February 1, 2022

More Information

Terms related to this study

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

No

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.

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