- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06282913
The Effect of Mindfulness Meditation
March 12, 2025 updated by: Buğse Yüceer, Gulhane Training and Research Hospital
The Effect of Mindfulness Meditation Practice on Compassion Fatigue, Burnout, and Psychological Well-Being of Health Professionals Working in Oncology Units: Randomized Controlled Study
Cancer is a disease that causes the most deaths worldwide and is challenging for patients and caregivers both physically and psychosocially.
Physicians and nurses working in oncology clinics perform a demanding profession providing compassionate care and treatment to patients struggling with life-threatening diseases.
The emotional cost of caring for patients diagnosed with cancer can lead to compassion fatigue, burnout, and decreased psychological well-being among healthcare professionals.
For this reason, this research is planned as a randomized controlled study to examine the effect of Mindfulness meditation practice on compassion fatigue, burnout, and psychological well-being in physicians and nurses working in oncology units.
Study Overview
Status
Not yet recruiting
Conditions
Intervention / Treatment
Study Type
Interventional
Enrollment (Estimated)
64
Phase
- Not Applicable
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Contact
- Name: Bugse Yuceer
- Phone Number: buseozgundondu34@gmail.com
- Email: buseozgundondu34@gmail.com
Study Locations
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-
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Ankara, Turkey
- Dr. Abdurrahman Yurtaslan Oncology Hospital
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Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
- Adult
- Older Adult
Accepts Healthy Volunteers
Yes
Description
Inclusion Criteria:
- Actively working in oncology clinics
- At least 1 year of working experience in an oncology clinic
- Not having a physical/mental/psychological disorder that would prevent participation in the research.
- Oncology nurses with a high school, undergraduate, associate or graduate degree in nursing
- Physicians and nurses who volunteer to participate in the research will be included in the research sample.
Exclusion Criteria:
- Physicians and nurses who have been diagnosed with a psychological disease in the last two years and are continuing their medical treatment • Physicians and nurses who did not agree to participate in the research
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Primary Purpose: Supportive Care
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Single
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Mindfulness Meditation Group
During the first meeting, before the planned training, data will be collected face to face using the personal information form, Compassion Fatigue Brief Scale, Maslach Burnout Scale, Psychological Well-Being Scale.
Physicians and nurses in the intervention group were given group counseling sessions by the researcher, in groups of 10-15 people, for 20 minutes once a week for 8 weeks.
An online meditation practice will be provided for a long time.
At the end of the mindfulness meditation application (in the 8th week) and four weeks after the end of the application (in the 12th week) for follow-up purposes, data will be collected through an online survey for physicians and nurses using Compassion Fatigue Brief Scale, Maslach Burnout Scale, Psychological Well-Being Scale.
|
Mindfulness Meditation application will be implemented online by the researcher in 20-minute group sessions once a week for 8 weeks.
Participants will be asked to provide a quiet, ventilated, dimly lit environment for the practice.
The researcher will start the application when the participants take their places as they feel comfortable.
In the first stage, the researcher will teach physicians and nurses to take deep diaphragmatic breaths through the nose and out through the mouth.
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No Intervention: Control Group
During the first meeting, data will be collected face to face using the personal information form, MY-KÖ, MTÖ and PİÖÖ.
In the 8th and 12th weeks of the research, the data will be re-administered to the physicians and nurses in the control group via an online survey using Compassion Fatigue Brief Scale, Maslach Burnout Scale, Psychological Well-Being Scale.
After the implementation process of the research is completed, mindfulness meditation application will be applied online once to the physicians and nurses in the control group.
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
compassion fatigue
Time Frame: up to 8 weeks
|
At the end of the mindfulness meditation practice in oncology physicians and nurses the Compassion Fatigue Brief Scale will be used to measure the changes in compassion fatigue.
As the scores obtained from the compassion fatigue brief scale increase, the perceived level of compassion fatigue in individuals increases.
The lowest score from the scale is 13 and the highest score is 130.
|
up to 8 weeks
|
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burnout
Time Frame: up to 8 weeks
|
At the end of the mindfulness meditation practice in oncology physicians and nurses the Maslach Burnout Scale will be used to measure the changes in the level of burnout.
Increasing Maslach Burnout Scale "Depersonalization" and "Emotional exhaustion" subscale scores indicate that burnout increases, while increasing the "personal success" subscale score indicates that burnout decreases.
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up to 8 weeks
|
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psychological well-being
Time Frame: up to 8 weeks
|
At the end of the mindfulness meditation practice in oncology physicians and nurses and the Psychological Well-Being Scale will be used to evaluate the changes in the level of psychological well-being.
A high score on the psychological well-being scale indicates that the person is at a positive level psychologically.
The highest score from the scale is 56, while the minimum score is 8.
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up to 8 weeks
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
compassion fatigue
Time Frame: up to 12 weeks
|
Four weeks after the end of the mindfulness meditation practice in oncology physicians and nurses the Compassion Fatigue Brief Scale will be used to measure the changes in compassion fatigue.
As the scores obtained from the compassion fatigue brief scale increase, the perceived level of compassion fatigue in individuals increases.
The lowest score from the scale is 13 and the highest score is 130.
|
up to 12 weeks
|
|
burnout
Time Frame: up to 12 weeks
|
Four weeks after the end of the mindfulness meditation practice in oncology physicians and nurses the Maslach Burnout Scale will be used to measure the changes in the level of burnout.
Increasing Maslach Burnout Scale "Depersonalization" and "Emotional exhaustion" subscale scores indicate that burnout increases, while increasing the "personal success" subscale score indicates that burnout decreases.
|
up to 12 weeks
|
|
psychological well-being
Time Frame: up to 12 weeks
|
Four weeks after the end of the mindfulness meditation practice in oncology physicians and nurses and the Psychological Well-Being Scale will be used to evaluate the changes in the level of psychological well-being.
A high score on the psychological well-being scale indicates that the person is at a positive level psychologically.
The highest score from the scale is 56, while the minimum score is 8.
|
up to 12 weeks
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (Estimated)
May 1, 2025
Primary Completion (Estimated)
November 1, 2025
Study Completion (Estimated)
December 1, 2025
Study Registration Dates
First Submitted
January 9, 2024
First Submitted That Met QC Criteria
February 21, 2024
First Posted (Actual)
February 28, 2024
Study Record Updates
Last Update Posted (Actual)
March 25, 2025
Last Update Submitted That Met QC Criteria
March 12, 2025
Last Verified
March 1, 2025
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- ---Oncology-Nursing-2024---
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
NO
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
product manufactured in and exported from the U.S.
No
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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