Psychological Effects of the Pandemic on the Health Personnel Working in the Filiation Team

April 27, 2023 updated by: Hacer Gok Ugur, T.C. ORDU ÜNİVERSİTESİ

Investigation Of The Psychological Effects of The Covid-19 Pandemic Process on The Health Staff Working in The Filation Team: A Mıxed Method Study

Purpose of Research: This study; It will be done in order to determine the psychological effects of the Covid-19 pandemic process on the health personnel working in the filiation team and to examine the possible effects in depth.

This research was planned as a mixed methods research. Research Questions

  1. What are the psychological effects of the pandemic process on the healthcare personnel working in the filiation team?
  2. Do the socio-demographic characteristics of the healthcare personnel working in the injection team affect their psychological status?
  3. What are the opinions of the health personnel working in the filtering team about the psychological effects of the pandemic?

Study Overview

Detailed Description

Type of Research This research was planned as a mixed methods research. Mixed methods research is a type of research that allows us to obtain in-depth information from the data collected by quantitative and qualitative data collection techniques. It also defines it as a research approach in which quantitative and qualitative data are collected in order to understand research problems and two data sets are integrated with each other. In this approach, a better understanding of the problem is provided by combining statistical trends with stories and personal experiences (Yıldırım & Şimşek, 2011).

Research Pattern The design of this research was determined as an explanatory sequential mixed design, one of the mixed methods research designs. Creswell (2009) states that deciding on a mixed method design depends on four factors: timing (simultaneous-sequential), weight (qualitative-quantitative), when and how it is mixed (connected-integrative-embedded), and theorizing. In this study, the explanatory sequential mixed design, which is dependent on the timing factor, was adopted from the designs determined by Creswell and Plano Clark (2011). The purpose of adopting this design in the research is to explain the quantitative data to be collected in more depth with qualitative data. According to the exploratory sequential mixed design, in the research, first of all, the "Effect of Events Scale" will be applied to determine the psychological effects of the pandemic process on the healthcare personnel working in the filiation team, and then "Semi-Structured Interviews" will be conducted with questions to be prepared with the data obtained from the scale in order to investigate the reasons for the results from this scale. The exploratory sequential mixed pattern is shown as NIC nit. This pattern is expressed as a useful pattern when qualitative data are needed to explain quantitative results (Creswell & Guetterman, 2018).

Study Type

Observational

Enrollment (Actual)

163

Contacts and Locations

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

Study Contact

  • Name: Hacer GÖK UĞUR, Assoc. Dr.
  • Phone Number: 6432 +904522265200
  • Email: hacer32@gmail.com

Study Contact Backup

  • Name: Muhammet ÖZKÖROĞLU, M.Sc.
  • Phone Number: 6432 +904522265200
  • Email: mhmmtozk@gmail.com

Study Locations

    • Altınordu
      • Ordu, Altınordu, Turkey, 52000
        • Hacer GÖK UĞUR

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

Yes

Sampling Method

Probability Sample

Study Population

Health personnel working in the filiation team

Description

Inclusion Criteria:

  • Worked in the filiation team,
  • Open to communication and cooperation, and
  • Healthcare personnel who agree to participate in the study will be included in the study.

Exclusion Criteria:

  • Healthcare personnel who worked during the filiation process but resigned due to various reasons such as retirement will be excluded from the study.

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

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Impact of Events Scale
Time Frame: 1.Day
The scale developed by Weiss and Marmara (1997) was translated into Turkish by Çorapçıoğlu et al. (2006) Adapted by. The scale measures the subjective stress levels of individuals exposed to traumatic life events. The scale consists of 22 items, and each item is evaluated in a 5-point Likert type as (0) not at all, (1) a little, (2) moderate, (3) a lot, (4) a lot. A score between 0 and 88 is obtained from the scale, and a high score indicates that the person has a high level of post-traumatic stress disorder. The scale consists of three subscales: hyperarousal, avoidance, and re-experiencing. Reliving (questions 1, 2, 3, 6, 9, 14, 16, 20), Avoidance (questions 5, 7, 8, 11, 12, 13, 17, 22), and Overstimulation (4, 10, 15) , 18, 19, 21) are determined by these items.
1.Day

Collaborators and Investigators

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

Investigators

  • Principal Investigator: Hacer GÖK UĞUR, Assoc. Dr., T.C. ORDU ÜNİVERSİTESİ

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 15, 2022

Primary Completion (Actual)

June 1, 2022

Study Completion (Actual)

September 15, 2022

Study Registration Dates

First Submitted

February 3, 2022

First Submitted That Met QC Criteria

February 3, 2022

First Posted (Actual)

February 14, 2022

Study Record Updates

Last Update Posted (Actual)

April 28, 2023

Last Update Submitted That Met QC Criteria

April 27, 2023

Last Verified

April 1, 2023

More Information

Terms related to this study

Other Study ID Numbers

  • Ordu12345

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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