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Health PersonnelNCT05238194

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

An observational study of Health Personnel, run by Ordu University at 1 site in Turkey (Türkiye).

Completed

Finished. The study has ended and is not enrolling. Results may be posted on the official record.

Official record
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Trial summary

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. Read more about this study

Who is it for?
Any ageHealthy volunteers can take part
Conditions the study is for
Health Personnel
What is being tested?
The Psychological Effects of The Covid-19 Pandemic Process
How many people
163 participants
Where
1 siteTurkey (Türkiye)
Study dates
15 Feb 2022to 15 Sep 2022
Phase
Observational
Are there results?
None posted in the registry

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages Any age
  • All sexes
  • Healthy volunteers accepted
  • Child, Adult, Older adult

Study population: Health personnel working in the filiation team

Who may be able to join

  • 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.

Who cannot join

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

Trial locations and contacts

1 site in 1 country.

Turkey (Türkiye)1 site
  • Hacer GOK UGUR

    Ordu, Altınordu, 52000

Other trials in Turkey (Türkiye)

About this study

Official title: 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?
Read the 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).

Being tested
The Psychological Effects of The Covid-19 Pandemic Process
Keywords
Covid-19, Pandemic, Filiation, Health personnel, Psychological effect, Nursing, Trauma
Medical subject headings
COVID-19, Wounds and Injuries

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • The Psychological Effects of The Covid-19 Pandemic ProcessOther

    Investigation of The Psychological Effects of The Covid-19 Pandemic Process on The Health Staff Workıng in The Filation Team

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Impact of Events Scale

    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.

    Measured: 1.Day

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted14 Feb 2022
  2. Study start15 Feb 2022
  3. Primary completion1 Jun 2022
  4. Study completion15 Sep 2022

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Observational
Observational model
Other
Time perspective
Prospective
Enrolment
163 participants (actual)
IDs, dates and publications
ClinicalTrials.gov ID
NCT05238194
Sponsor's protocol ID
Ordu12345
Status last verified
Apr 2023
First submitted
3 Feb 2022
Last updated
28 Apr 2023
Results posted
No
Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
No

Questions about this trial

What is this clinical trial studying?

An observational study of Health Personnel, run by Ordu University at 1 site in Turkey (Türkiye).

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 3 inclusion and 1 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: finished, as of the sponsor's last update on 28 Apr 2023. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in Turkey (Türkiye). Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.

How can a doctor refer a patient or contact the research team?

The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Impact of Events Scale (time frame: 1.Day). It is what the study was designed to measure, not a finding.

Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 28 Apr 2023.

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