NCT06271278

Brief Summary

Nurses working in surgical intensive care units face numerous health and safety stressors. The introduction of new health technologies, medical devices (such as bedside monitors, pump and perfuser devices, and mechanical ventilators), and changing health environments have contributed to increased work stress among nurses. This, in turn, has had negative effects on their physical and mental health outcomes. One of the hazards associated with medical devices is alarm fatigue. Noise pollution caused by bells, beeps, and horns in intensive care units can lead to alarm fatigue, defined as desensitisation to monitor alarms. Nurses are particularly susceptible to this due to their constant exposure to these sounds, which can also cause stress. Occupational stress is a recognised issue in this demanding field, characterised by disproportionate workloads and negative effects on performance.Work-related stress can lead to a loss of compassion towards patients and an increase in malpractice, negatively affecting the quality of care. Thus, this study aimed to investigate the impact of applying emotional freedom techniques on work-related stress and alarm fatigue experienced by nurses working in surgical intensive care units.

Trial Health

87
On Track

Trial Health Score

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

Enrollment
144

participants targeted

Target at P75+ for not_applicable

Timeline
Completed

Started Nov 2023

Shorter than P25 for not_applicable

Geographic Reach
1 country

1 active site

Status
completed

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

November 2, 2023

Completed
3 months until next milestone

First Submitted

Initial submission to the registry

February 14, 2024

Completed
7 days until next milestone

First Posted

Study publicly available on registry

February 21, 2024

Completed
4 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

June 28, 2024

Completed
2 months until next milestone

Study Completion

Last participant's last visit for all outcomes

August 16, 2024

Completed
Last Updated

January 14, 2025

Status Verified

January 1, 2025

Enrollment Period

8 months

First QC Date

February 14, 2024

Last Update Submit

January 11, 2025

Conditions

Keywords

Surgical intensive careAlarm FatigueJob stressEmotional Freedom TechniqueSurgical nurse

Outcome Measures

Primary Outcomes (3)

  • Subjective Units of Disturbance Scale

    The discomfort scale used in energy therapies allows individuals to evaluate their own discomfort on a scale of 0 to 10, where 0 indicates no discomfort and 10 indicates unbearable discomfort.

    0-7 days tracking

  • Alarm Fatigue Scale

    The scale consists of 13 items and produces a score between 0 and 36. A higher score indicates an increase in alarm fatigue.

    0-7 days tracking

  • The General Work Stress Scale

    The General Work Stress Scale is a 9-item scale that produces scores ranging from 9 to 45. High scores indicate high job stress, while low scores indicate low job stress.

    0-7 days tracking

Study Arms (2)

Emotional Freedom Techniques group

EXPERIMENTAL

The Nurse Introduction Form, Subjective Discomfort Unit, Alarm Fatigue Scale, and Work Stress Scale were administered to the experimental group prior to patient care. The Emotional Freedom Technique was explained, and the nurses were instructed to apply it before and after their shifts for one week. One week later, the Subjective Discomfort Unit, Alarm Fatigue Scale, and Work Stress Scale were applied again.

Behavioral: Emotional Freedom Technique

Control group

NO INTERVENTION

No applications were administered to nurses working in the surgical intensive care unit. In the control group, data was collected before patient care using the Nurse Introduction Form, Subjective Discomfort Unit, Alarm Fatigue Scale, and Work Stress Scale. No interventions were performed. One week later, the Subjective Discomfort Unit, Alarm Fatigue Scale, and Work Stress Scale were applied again.

Interventions

Emotional Freedom Technique (EFT) is a powerful and effective practice that enables individuals to release negative emotions and achieve mental and physical relaxation. EFT is a form of counselling based on acupuncture points, which are areas of low electrical and energy flow in the body. Stimulating these points causes the brain to secrete dopamine. EFT involves stimulating specific points on the body where energy flow is low. This is done by gently tapping on these areas with the fingers, which releases dopamine. The process is painless and can be performed by the individual themselves.

Emotional Freedom Techniques group

Eligibility Criteria

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

You may qualify if:

  • Being 18 years of age or older
  • Working as a nurse in one of the surgical intensive care units
  • Volunteering to participate in the study

You may not qualify if:

  • Working in a unit other than surgical intensive care units
  • Not volunteering to participate in the research

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Inonu University Turgut OzaL Medical Center

Malatya, 44090, Turkey (Türkiye)

Location

MeSH Terms

Conditions

Occupational StressAlert Fatigue, Health Personnel

Condition Hierarchy (Ancestors)

Occupational DiseasesStress, PsychologicalBehavioral SymptomsBehaviorMental FatigueFatigueSigns and SymptomsPathological Conditions, Signs and Symptoms

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
TRIPLE
Who Masked
PARTICIPANT, INVESTIGATOR, OUTCOMES ASSESSOR
Masking Details
Participants will be blinded to their group assignment. The subjects will be selected in a randomized order using software. Data collection will be conducted without involvement from research analysts.
Purpose
SUPPORTIVE CARE
Intervention Model
PARALLEL
Model Details: This study was conducted as a randomised controlled study with experimental and control groups.
Sponsor Type
OTHER
Responsible Party
SPONSOR INVESTIGATOR
PI Title
Assistant Professor

Study Record Dates

First Submitted

February 14, 2024

First Posted

February 21, 2024

Study Start

November 2, 2023

Primary Completion

June 28, 2024

Study Completion

August 16, 2024

Last Updated

January 14, 2025

Record last verified: 2025-01

Data Sharing

IPD Sharing
Will not share

Locations