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Effect of a Mindfulness Training Program on Surgical Nurses

NCT07553169 · Status: ENROLLING_BY_INVITATION · Phase: NA · Type: INTERVENTIONAL · Enrollment: 76

Last updated 2026-04-30

No results posted yet for this study

Summary

This randomized controlled single-blind study aims to evaluate the effect of mindfulness training on mindfulness levels, psychological resilience, and work motivation among surgical nurses. Surgical nurses work in highly demanding environments characterized by complex patient care processes, unpredictable complications, and intensive workloads, which may negatively affect their psychological resilience and work motivation. Mindfulness-based interventions have been reported to improve psychological well-being, coping strategies, and professional functioning among healthcare professionals.

The study will be conducted with nurses working in surgical clinics at Afyonkarahisar Health Sciences University Health Practice and Research Center. Eligible nurses will be randomly assigned to either an experimental group receiving mindfulness training or a control group receiving no intervention. The mindfulness training program will be delivered over four weeks, consisting of two sessions per week, each lasting 40 minutes.

Data will be collected using the Mindful Attention Awareness Scale (MAAS), Connor-Davidson Resilience Scale Short Form (CD-RISC-10), and Nurses' Work Motivation Scale. Measurements will be performed at baseline and four weeks after completion of the training program. The findings of this study are expected to contribute to improving psychological resilience, mindfulness, and work motivation among surgical nurses and support the development of effective supportive care interventions in clinical settings.

Conditions

  • Mindfulness Training

Interventions

BEHAVIORAL

Mindfulness Training

Participants receive mindfulness training sessions delivered according to the study protocol.

Sponsors & Collaborators

  • SELDA MERT

    lead OTHER

Principal Investigators

  • Özlem Kersu, PhD · Eskisehir Osmangazi University

Study Design

Allocation
RANDOMIZED
Purpose
SUPPORTIVE_CARE
Masking
SINGLE
Model
PARALLEL

Eligibility

Min Age
18 Years
Max Age
65 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2026-02-16
Primary Completion
2026-04-30
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 NCT07553169 on ClinicalTrials.gov