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Not yet recruiting NCT07359365

The Effect of Breathing Exercises on Compassion Fatigue and Work Tress Among Emergency Department Nurses

No phase Interventional Work Stress

For patients and families

In plain language

An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.

What is being studied
The protocol lists: Breathing Exercise Training, usual care.
Who it may be relevant to
Registry conditions: Work Stress. Basic parameters: from 18 years · All.
What needs checking
Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
Where it takes place
Turkey (Türkiye)
Next step
Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
Official title

The Effect of Breathing Exercises on Compassion Fatigue and Work Stress Among Emergency Department Nurses: A Randomized Controlled Trial

Overview

The purpose of this randomized controlled study is to examine the effect of breathing exercises on compassion fatigue and work stress among emergency department nurses

Detailed description

"This study will be conducted with nurses working in the emergency department. Participants will be randomly assigned to either an intervention group receiving breathing exercise training or a control group. Data will be collected using a sociodemographic data form and validated scales measuring work stress and compassion fatigue. The aim of the study is to evaluate the effect of breathing exercises on work stress and compassion fatigue levels among emergency department nurses."

Interventions

  • Behavioral Breathing Exercise Training
    Participants in the experimental group will receive training on proper breathing techniques and breathing exercise methods. Each session will last 30-40 minutes. Sessions will be conducted twice a week for a total of 4 weeks.
  • Other usual care
    No intervention will be applied. Participants in the control group will continue their usual routine.

Primary outcome measures

  • Compassion Fatigue Score [Time frame: Baseline and 8 weeks]
  • Work Stress Score [Time frame: Baseline and 4 weeks after ınvertıon]

Eligibility criteria

Inclusion criteria

  • Currently employed as an emergency department nurse.
  • No diagnosed psychiatric disorders.
  • No prior participation in breathing exercise programs.

Exclusion criteria

  • Presence of respiratory system disease.
  • Physical conditions that prevent participation in breathing exercises.
  • Working outside the emergency department.

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: No

Study design

Allocation
Randomized
Model
Parallel assignment
Masking
Open label
Primary purpose
Other

Study locations

Turkey (Türkiye) · 1 center
  • Çanakkale Onsekiz Mart University — Çanakkale

Identifiers

NCT: NCT07359365 · CanakkaleOMU-SBF-BAE-01

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗