NCT05758636

Brief Summary

It is very important to protect and improve the physical, mental and social health of nurses, especially in the event that nurses frequently encounter patients diagnosed or suspected of COVID-19 and are exposed to the virus for a long time due to the long duration of care, increasing cases and the death of their colleagues. Que et al., 2020). Current researches have made it necessary for nurses to have difficulties in effectively coping with the anxiety experienced in the COVID-19 pandemic, which has affected the whole world, and to apply new effective methods, as their training includes effective coping methods (Feinstein and Church, 2010). There are studies that are effective in reducing stress and anxiety, such as meditation, yoga, and breathing therapies, which are recommended to prevent the increase in stress and anxiety levels that may occur in nurses by evaluating the experienced situations (Labrague et al., 2020; Vieta et al., 2020). In addition to these applications, it is seen that Emotional Freedom Technique (EFT) has been increasingly used recently in controlling and reducing anxiety (Hartmann, 2016). EFT is a type of energy-based psychotherapy that combines the components of Western psychology and Eastern medicine, applied to eliminate negative thoughts and feelings and problems related to emotions (İnangil et al., 2020; Church, 2013). Although the EFT technique is used in many different areas today, its effect on the level of anxiety in nurses during the COVID-19 process is not yet known. As a result, to evaluate the effect of EFT, whose positive results have been proven by many studies, on the anxiety level of nurses caring for COVID-19 patients.

Trial Health

43
At Risk

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Trial has exceeded expected completion date
Enrollment
100

participants targeted

Target at P50-P75 for not_applicable

Timeline
Completed

Started Mar 2022

Geographic Reach
1 country

1 active site

Status
unknown

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

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Study Timeline

Key milestones and dates

Study Start

First participant enrolled

March 2, 2022

Completed
7 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

September 25, 2022

Completed
5 months until next milestone

First Submitted

Initial submission to the registry

March 4, 2023

Completed
3 days until next milestone

First Posted

Study publicly available on registry

March 7, 2023

Completed
3 months until next milestone

Study Completion

Last participant's last visit for all outcomes

June 1, 2023

Completed
Last Updated

March 7, 2023

Status Verified

March 1, 2023

Enrollment Period

7 months

First QC Date

March 4, 2023

Last Update Submit

March 4, 2023

Conditions

Outcome Measures

Primary Outcomes (1)

  • Spielberger state-trait anxiety scale

    While the Trait Anxiety Inventory aims to determine how the individual feels independently of the situation and conditions, the State Anxiety Inventory aims to determine how the individual feels at a certain moment and under certain conditions. Both subscales are four-point Likert-type scales consisting of twenty items. In the State Anxiety Inventory, the individual is asked to evaluate how he or she feels at the moment, according to the situation he is in, and to choose one of the expressions "1-not at all, 2-somewhat, 3-a lot and 4-completely" according to the severity of the emotions or behaviors expressed in the items. The highest score of 4 is given for choosing the phrase "completely", and the lowest score is 1 for choosing the phrase "not at all".

    4 months

Secondary Outcomes (1)

  • SUE (Subjective Units of Experience) Scale

    4 months

Study Arms (2)

Emotional Freedom Technique Group

EXPERIMENTAL

Nurses (40) enrolled in the emotional freedom technique group will receive a total of 4 rounds of EFT, 50 minutes, 3 days a week.

Behavioral: Emotional Freedom Technique

Control

NO INTERVENTION

Participants in the control group (n= 40) will not receive intervention throughout the study.

Interventions

Before starting the EFT session, the participants were asked to identify the problem that aroused their anxiety. After the common point of the problems was determined, the ORDS level of all participants was determined. Next, the EFT session explained traditional acupressure meridian points on the head, face, neck, chest, and hands. Next, they were asked to repeat the phrase, "Even though I have this feeling of stress and anxiety, I accept myself deeply and completely," while gently applying to the acupuncture points with their index and middle fingers. While using this expression, the participants hit each acupuncture area seven times. After the first round of hits accompanied by this phrase, participants were asked to abbreviate "this feeling of anxiety, stress" with another short phrase. The participants then repeated rounds of this process until they noticed that their anxiety had decreased

Emotional Freedom Technique Group

Eligibility Criteria

Age18 Years+
Sexall
Healthy VolunteersYes
Age GroupsAdult (18-64), Older Adult (65+)

You may qualify if:

  • not having been diagnosed with a psychiatric diagnosis,
  • not having received any therapy including coping with stress
  • not being diagnosed with COVID-19
  • not being in the treatment care process
  • not having applied the emotional freedom technique before, and volunteering to participate

You may not qualify if:

  • Not participating in any of the emotional freedom technique sessions
  • Being diagnosed with COVID-19 during the application of therapy

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Marmara University

Istanbul, Kadikoy, 34722, Turkey (Türkiye)

Location

MeSH Terms

Conditions

Anxiety Disorders

Condition Hierarchy (Ancestors)

Mental Disorders

Study Officials

  • Şule Ecevit Alpar, Phd

    Marmara University

    STUDY DIRECTOR

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
DOUBLE
Who Masked
PARTICIPANT, CARE PROVIDER
Purpose
HEALTH SERVICES RESEARCH
Intervention Model
PARALLEL
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Phd Candidate

Study Record Dates

First Submitted

March 4, 2023

First Posted

March 7, 2023

Study Start

March 2, 2022

Primary Completion

September 25, 2022

Study Completion

June 1, 2023

Last Updated

March 7, 2023

Record last verified: 2023-03

Data Sharing

IPD Sharing
Will not share

Locations