Emotional Awareness and Communication Training Effectiveness in Oncology Nurses

Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18+
SponsorAnkara Yildirim Beyazıt University

About this trial

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.

Eligibility criteria

This trial accepts healthy volunteers

Qualifiers

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

Disqualifiers

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

Trial design

Design model

Parallel

Treatments tested in this trial

  • Structured Emotional Awareness and Communication Training

    Behavioral

    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.

  • Educational Materials

    Other intervention

    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.

Treatment groups

64 Participants
are divided into 2 treatment groups
Group A: Intervention GroupExperimental treatment 1 intervention
Group B: Control GroupOther 1 intervention

Trial outcomes

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.

Time frame
Baseline and 4 weeks after the intervention

Secondary outcomes

1

Change in Compassion Fatigue Levels

Compassion fatigue will be evaluated using the Professional Quality of Life Scale (ProQOL) at baseline and 4 weeks after the intervention.

Time frame
Baseline and 4 weeks after the intervention
2

Change in Emotional Awareness and Communication Skills

Emotional awareness and communication skills will be measured using a researcher-developed questionnaire at baseline and 4 weeks after the intervention.

Time frame
Baseline and 4 weeks after the intervention

Other outcomes

Sponsors and contacts

Click on the lead sponsor to view all of their trials.

Ankara Yildirim Beyazıt University

Lead sponsor

Ankara Etlik City Hospital

Collaborator