- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05158504
The Effect of Motivational Messages on Emergency Nurses
The Effects of Motivational Messages Sent to Emergency Nurses During the COVID-19 Pandemic on Job Satisfaction, Compassion Fatigue, and Communication Skills: A Randomized Controlled Trial
Aim and objectives: The aim of this study is to examine the effect of motivational notifications applied to emergency nurses on job satisfaction, compassion fatigue and communication skills during the COVID-19 pandemic.
Background: Emergency room nurses working on the front lines during the COVID-19 pandemic; many factors such as excessive workload, prolonged working hours, threat of infection, death of the patients they care for have caused them to experience physical, social and psychological problems.
Design: It is a randomized controlled, open-label study. Methods: This study was carried out with a total of 60 nurses working in the emergency units of two training and research hospitals in Istanbul. Participants were divided into motivational group and control group. Motivational notifications were sent via Short Message Service (SMS) to the mobile phones of the participants in the motivational group (n=30) for 21 days. No motivational notification was sent to the control group (n=30) during this process. Data were obtained with the Individual Introduction Form, Job Satisfaction, Compassion Fatigue and Communication Skills Scale.
Study Overview
Status
Conditions
Intervention / Treatment
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
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Beylikdüzü
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Istanbul, Beylikdüzü, Turkey
- Hilal KARTAL
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Description
Inclusion Criteria:The nurses working in the emergency room, working only in the day shift on weekdays, using mobile phones and volunteering to participate in the study were included in the study.
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Exclusion Criteria: Exclusion criteria for the study included being on leave for any reason (maternity, annual, medical) during the study dates, not completely filling in the data collection forms, or withdrawing from the study.
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Study Plan
How is the study designed?
Design Details
- Primary Purpose: Prevention
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
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Experimental: Motivation
Motivational notifications were sent to the nurses in the motivational group (n=30) via SMS messages to their mobile phones at 07.00, 12.00 and 16.00 for 21 days.
Like a good morning message that allows you to start the day with a beautiful energy (Example: Thank you for the hard and selfless work you do every day.
We love and appreciate angels like you and you.
Good morning).
Motivational notifications sent to the participants were prepared each day to be different from the previous day.
Data were obtained with the Individual Introduction Form, Job Satisfaction, Compassion Fatigue and Communication Skills Scale.
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Motivational notifications were sent via SMS message to the nurses in the motivation group (n=30) at 07.00, 12.00 and 16.00 for 21 days.
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No Intervention: Control
Motivational notifications were not sent to the nurses in the control group (n=30) and they continued their routine work in the emergency room.
only pretest and posttest were applied.
Data were obtained with the Individual Introduction Form, Job Satisfaction, Compassion Fatigue and Communication Skills Scale.
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Job Satisfaction-Short Scale
Time Frame: Baseline and after 3 weeks
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Job satisfaction scale is in a 5-point Likert type and is graded as (1- Absolutely disagree and 5-Absolutely agree).
Scoring of the scale is calculated as a minimum of 1 and a maximum of 5 points, and the average of 5 related items is taken.
The lowest score that can be obtained from the scale is 5 and the highest score is 25.
Accordingly, the decrease in the average score of the participants indicates that job satisfaction decreases; an increase in the average score indicates an increase in job satisfaction.
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Baseline and after 3 weeks
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Compassion Fatigue-Short Scale
Time Frame: Baseline and after 3 weeks
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The scale aims to measure secondary trauma and occupational burnout.
Items are rated on a 10-point Likert-type scale ranging from rarely/never (1) to very often (10).
The total possible score ranges from 13 to 130, with higher scores representing a higher level of compassion fatigue.
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Baseline and after 3 weeks
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Communication Skills Scale
Time Frame: Baseline and after 3 weeks
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This scale was developed to determine how people evaluate their own communication skills.
It consists of 25 items on a 5-point Likert-type scale ranging from always (1) to never (5).
The scale yields a score ranging from 25 to 125.
High scores reflect a positive perception of the person's communication skills.
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Baseline and after 3 weeks
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Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Compassion Fatigue-Short Scale
Time Frame: Three weeks
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Rarely/never (1) and often (10) is a 10-point Likert type, with the smallest 13 and the highest 130 points.
As the scores obtained from the scale increase, the level of compassion fatigue experienced by individuals increases.
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Three weeks
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Communication Skills Scale
Time Frame: Three weeks
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The scale is a 5-point Likert-type scale, graded from "always" to "never".
The scale consists of a total of 25 expressions and the highest score that can be obtained is 125 and the lowest score is 25.
High scores reflect that individuals evaluate their communication skills positively.
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Three weeks
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Collaborators and Investigators
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- SBU-HAMIDIYE-KARTAL-00001-2021
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
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