- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05606861
Mindfulness Based Interventions in Pediatric Nurses (PRoNMBSR)
Effect of Mindfulness Based Stres Reduction Intervention on Psychological Resilience of Child Nurses: Randomized Controlled Trial
The aim of the study was to evaluate the effect of the Mindfulness Stress Reduction Intervention on increasing the psychological resilience of pediatric nurses.
Design: This is a single-center, single-blind, randomized controlled trial
Method:
In the study, the group in which the Mindfulness-Based Stress Reduction Initiative was applied was taken as the experimental (n: 15), the unstructured group (n: 14) in which the stressful life experiences were shared as the control group. Due to the limited number of the research population (N:56), 29 nurses who agreed to participate in the study and met the inclusion criteria were included in the study without using the sampling method. This research was conducted with pediatric nurses working in the inpatient units of a children's hospital affiliated to a university in Izmir. Stress reduction training based on mindfulness, including meditation and breathing techniques, was given to the experimental group for 5 weeks. No intervention was applied to the control group.
The primary outcomes of the study were measured using the Perceived Stress Scale, the Self-Compassion Scale, the Interpersonal Reactivity Index, and Psychological Resilience Scale for Adults.
This study is important because it is the first randomized controlled study on the effect of Mindfulness Based Stress Reduction (MBSR) on resilience in nurses in our country.
In addition, the results will contribute to preventing nurses from leaving the profession in the early period, providing more flexibility and therefore safe patient care to the nursing workforce, especially in today's health system where there is a heavy nursing shortage.
Study Overview
Status
Conditions
Intervention / Treatment
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
-
-
-
İzmir, Turkey, 35100
- Ege University Hospital
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Description
Inclusion Criteria:
- Working for at least one year in the children's ward,
- Older than 18 years of age,
- The working program must be suitable for the experiment schedule.
Exclusion Criteria:
- Clinical diagnosis for a psychiatric disorder,
- Long experience of meditation or yoga.
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Prevention
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Double
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Intervention group
Mindfulness Based Intervention in pediatric nurses components was applied to this group.
|
This intervention are structured mindfulness program including meditation and breathing techniques .
|
|
No Intervention: Control group
No procedure was conducted the control group.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Perceived Stress Level
Time Frame: For 9 weeks
|
Perceived Stress Scale:The lowest score which can be obtained on the scale is 0, and the highest is 56.Higher total score means higher perceived stress level.
|
For 9 weeks
|
|
Psychological Resilience Level
Time Frame: For 9 weeks
|
Psychological Resilience Scale for Adults: The minimum score on the scale is 33, and the maximum is 165.
A low score on the scale indicates that the person's psychological resilience level is inadequate.
|
For 9 weeks
|
|
Empathy Level
Time Frame: For 9 weeks
|
Interpersonal Reactivity Index: The scale measures different aspects of empathy.
For example, the perspective-taking dimension expresses better interpersonal functioning and higher self-esteem, while the empathetic thinking dimension expresses a consistent relationship with social competence or self-esteem.
|
For 9 weeks
|
|
Self Compassion Level
Time Frame: For 9 weeks
|
The Self-Compassion Scale consists of 26 Likert type items and six sub-dimensions.A higher total score on the scale indicates a higher level of self-compassion perceived by the participants.
|
For 9 weeks
|
Collaborators and Investigators
Sponsor
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
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
- 69631334-300
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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