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Emotional Awareness and Communication Training Effectiveness in Oncology Nurses

NCT07231913 · Status: RECRUITING · Phase: NA · Type: INTERVENTIONAL · Enrollment: 64

Last updated 2025-11-17

No results posted yet for this study

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.

Conditions

  • Occupational Burnout
  • Emotional Awareness
  • Communication Skills

Interventions

BEHAVIORAL

Structured Emotional Awareness and Communication Training

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.

OTHER

Educational Materials

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.

Sponsors & Collaborators

  • Ankara Etlik City Hospital

    collaborator OTHER_GOV

  • Ankara Yildirim Beyazıt University

    lead OTHER

Study Design

Allocation
RANDOMIZED
Purpose
SUPPORTIVE_CARE
Masking
NONE
Model
PARALLEL

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2025-10-25
Primary Completion
2026-01-31
Completion
2026-05-31

Countries

  • Turkey (Türkiye)

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT07231913 on ClinicalTrials.gov