- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT07553169
Effect of a Mindfulness Training Program on Surgical Nurses
The Effect of a Mindfulness Training Program on Surgical Nurses' Psychological Resilience, Work Motivation, and Cognitive Awareness: A Randomized Controlled Trial
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.
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
Nurses constitute a fundamental component of healthcare systems and play a critical role in maintaining, promoting, and improving individual and community health. Surgical nurses, in particular, work in complex and dynamic environments requiring rapid decision-making, management of high-risk situations, and continuous patient monitoring. The unpredictable nature of surgical patient outcomes and the occurrence of unexpected complications may increase stress levels and negatively affect nurses' psychological resilience and work motivation.
Psychological resilience refers to an individual's ability to recover from stressful or adverse experiences and adapt effectively to challenging conditions. Several internal and external factors influence resilience, including emotional awareness, coping skills, social relationships, and cognitive awareness. Among these factors, mindfulness has been identified as a significant contributor to psychological resilience and psychological well-being. Mindfulness is defined as the ability to focus attention on the present moment in a non-judgmental and accepting manner. Mindfulness-based practices, such as breathing exercises and meditation, promote emotional regulation, stress management, and cognitive flexibility.
Previous studies have demonstrated that mindfulness-based interventions improve anxiety levels, reduce burnout, enhance job satisfaction, and support emotional well-being among healthcare professionals. However, limited evidence exists regarding the combined effects of mindfulness training on mindfulness levels, psychological resilience, and work motivation among surgical nurses. Considering the demanding and stressful nature of surgical settings, interventions aimed at improving nurses' psychological well-being may positively influence both professional performance and quality of care.
This study is designed as a single-blind randomized controlled trial to evaluate the effectiveness of a structured mindfulness training program among surgical nurses. The study population will consist of nurses working in surgical clinics at Afyonkarahisar Health Sciences University Health Practice and Research Center. Participants who meet the inclusion criteria and provide informed consent will be randomly assigned to either the experimental or control group using a computer-based randomization method.
Participants in the experimental group will receive a structured mindfulness training program delivered by a certified mindfulness trainer. The program will be conducted over four weeks, with two sessions per week, each lasting 40 minutes. Participants will be grouped into small groups of approximately ten individuals to facilitate interaction and learning. The control group will not receive any intervention during the study period.
Data will be collected using validated measurement tools. Sociodemographic data will be collected using a Personal Information Form. Mindfulness levels will be measured using the Mindful Attention Awareness Scale (MAAS), psychological resilience will be assessed using the Connor-Davidson Resilience Scale Short Form (CD-RISC-10), and work motivation will be measured using the Nurses' Work Motivation Scale. Baseline measurements will be performed before the intervention, and post-intervention measurements will be conducted four weeks after completion of the mindfulness training program.
The outcome assessor will be blinded to group allocation to reduce assessment bias. The primary outcome of the study will be mindfulness level, while psychological resilience and work motivation will be evaluated as secondary outcomes.
The findings of this study are expected to provide evidence regarding the effectiveness of mindfulness-based supportive interventions for surgical nurses. The results may contribute to improving nurses' psychological resilience, enhancing work motivation, and supporting occupational well-being in surgical clinical settings. Furthermore, the outcomes of this research may guide the development of structured supportive care programs aimed at strengthening nurses' professional performance and psychological health.
Study Type
Enrollment (Estimated)
Phase
- Not Applicable
Contacts and Locations
Study Locations
-
-
-
Afyonkarahisar, Turkey (Türkiye)
- Afyonkarahisar University of Health Sciences Health Application and Research Center
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Adult
- Older Adult
Accepts Healthy Volunteers
Description
Inclusion Criteria:
- working as a nurse in a surgical clinic
- volunteering to participate in the study
Exclusion Criteria:
- not volunteering to participate in the study
- having previously received cognitive awareness training
Study Plan
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: Structured Mindfulness Training
Participants receive a structured mindfulness training program.
|
Participants receive mindfulness training sessions delivered according to the study protocol.
|
|
No Intervention: Standard Care (No Mindfulness Training)
Participants receive standard care without mindfulness training.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Mindfulness Level
Time Frame: Baseline and 4 weeks after completion of the mindfulness training program
|
Midfulness level will be assessed using the Mindful Attention Awareness Scale (MAAS).
The scale consists of 15 items rated on a 6-point Likert scale.
Higher scores indicate higher levels of mindfulness.
The total score ranges between 15 and 90.
A high score on the scale indicates a high level of mindfulness.
|
Baseline and 4 weeks after completion of the mindfulness training program
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Psychological Resilience
Time Frame: Baseline and 4 weeks after completion of the mindfulness training program
|
Psychological resilience will be assessed using the Connor-Davidson Resilience Scale Short Form (CD-RISC-10).
The scale consists of 10 items rated on a 5-point Likert scale.
Higher scores indicate higher levels of psychological resilience.
|
Baseline and 4 weeks after completion of the mindfulness training program
|
|
Work Motivation
Time Frame: Baseline and 4 weeks after completion of the mindfulness training program
|
Work motivation will be assessed using the Nurses' Work Motivation Scale.
The scale Short Form (CD-RISC-10).
The scale consists of 10 items rated on a 5-point Likert scale.
Higher scores indicate higher levels of psychological resilience.consists of 25 items rated on a 3-point Likert scale.
Higher scores indicate higher levels of work motivation.
|
Baseline and 4 weeks after completion of the mindfulness training program
|
Collaborators and Investigators
Sponsor
Investigators
- Principal Investigator: Özlem Kersu, PhD, Eskisehir Osmangazi University
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Estimated)
Study Completion (Estimated)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Other Study ID Numbers
- 2025/15
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
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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