Emotional Awareness and Communication Training Effectiveness in Oncology Nurses
Evaluation of the Effectiveness of Emotional Awareness and Communication-Based Intervention Training for Oncology Nurses
1 other identifier
interventional
64
1 country
1
Brief Summary
This interventional clinical study aims to evaluate whether a structured emotional awareness and communication training program can reduce occupational burnout among oncology nurses. The study will address the following primary questions: Does the intervention lead to a significant increase in nurses' emotional awareness? Does it improve their communication skills in challenging patient and family interactions? Does it reduce their levels of professional burnout? Participants will be recruited from oncology nurses working at Ankara Etlik City Hospital who have been employed in the unit for at least six months and consent to participate. A total of 64 nurses will be randomly assigned to an intervention group (n=32), receiving four weekly face-to-face training sessions over four weeks, or a control group (n=32), receiving educational materials in written/digital format. Data will be collected using pre- and post-intervention assessments with the Maslach Burnout Inventory, the Emotional Requirements Scale, and the Communication Skills Scale for Healthcare Professionals. All data will be anonymized and analyzed to determine the effectiveness of the intervention in enhancing emotional awareness and communication skills and in reducing burnout among oncology nurses.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P50-P75 for not_applicable
Started Oct 2025
Shorter than P25 for not_applicable
1 active site
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
October 25, 2025
CompletedFirst Submitted
Initial submission to the registry
November 14, 2025
CompletedFirst Posted
Study publicly available on registry
November 17, 2025
CompletedPrimary Completion
Last participant's last visit for primary outcome
January 1, 2026
CompletedStudy Completion
Last participant's last visit for all outcomes
May 1, 2026
CompletedNovember 17, 2025
November 1, 2025
2 months
November 14, 2025
November 14, 2025
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
Change in Burnout Levels of Oncology Nurses
Burnout levels will be assessed using the Maslach Burnout Inventory (MBI) before and 4 weeks after the intervention.
Baseline and 4 weeks after the intervention
Secondary Outcomes (2)
Change in Compassion Fatigue Levels
Baseline and 4 weeks after the intervention
Change in Emotional Awareness and Communication Skills
Baseline and 4 weeks after the intervention
Study Arms (2)
Intervention Group
EXPERIMENTALParticipants receive a structured emotional awareness and communication training program over four weeks, with weekly 45-minute face-to-face sessions covering emotional recognition, coping with burnout, effective communication in challenging situations, and personal strategies to prevent burnout.
Control Group
OTHERParticipants receive educational materials in written/digital format after the intervention period. No face-to-face training is provided during the study.
Interventions
Participants in the intervention group will receive a structured training program over four weeks, consisting of weekly 45-minute face-to-face sessions. The program covers: Recognizing emotions and emotional awareness Burnout symptoms and healthy coping strategies Challenging conversations and effective communication skills Personal strategies to prevent burnout The training includes interactive presentations, group discussions, and short exercises.
Participants in the control group will receive written or digital educational materials after the intervention period. No face-to-face training is provided during the study.
Eligibility Criteria
You may qualify if:
- Employed as a nurse in an oncology unit for at least 6 months
- Voluntarily agrees to participate in the study
- Able to attend all training sessions
- Completes both pre-test and post-test questionnaires
You may not qualify if:
- Currently on leave or planning to take leave during the study period
- Has received prior structured training related to emotional awareness or communication skills within the past year
- Diagnosed with a severe psychological disorder that may affect participation
Contact the study team to confirm eligibility.
Sponsors & Collaborators
- Ankara Yildirim Beyazıt Universitylead
- Ankara Etlik City Hospitalcollaborator
Study Sites (1)
Ankara Etlik City Hospital
Ankara, Yenimahalle, 06170, Turkey (Türkiye)
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Central Study Contacts
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- NONE
- Masking Details
- This study is open-label. Participants and researchers are aware of group assignments because the intervention involves face-to-face training sessions, which cannot be blinded. Outcome assessments will be conducted using standardized self-report questionnaires. All data will be anonymized during analysis to minimize bias.
- Purpose
- SUPPORTIVE CARE
- Intervention Model
- PARALLEL
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- MSc Student, Ankara Yıldırım Beyazıt University, Department of Mental Health and Disease Nursing
Study Record Dates
First Submitted
November 14, 2025
First Posted
November 17, 2025
Study Start
October 25, 2025
Primary Completion
January 1, 2026
Study Completion
May 1, 2026
Last Updated
November 17, 2025
Record last verified: 2025-11
Data Sharing
- IPD Sharing
- Will not share
Data collected will be anonymized and used solely for this study. Individual participant data will not be shared outside the research team.