Mindfulness Based Interventions in Pediatric Nurses (PRoNMBSR)

November 3, 2022 updated by: Tülün Liman, Ege University

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

Completed

Conditions

Study Type

Interventional

Enrollment (Actual)

29

Phase

  • Not Applicable

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

      • İzmir, Turkey, 35100
        • Ege University Hospital

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

14 years to 54 years (Adult)

Accepts Healthy Volunteers

No

Genders Eligible for Study

All

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

This section provides details of the study plan, including how the study is designed and what the study is measuring.

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

This is where you will find people and organizations involved with this study.

Sponsor

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

November 20, 2018

Primary Completion (Actual)

December 28, 2018

Study Completion (Actual)

January 30, 2019

Study Registration Dates

First Submitted

October 25, 2022

First Submitted That Met QC Criteria

November 3, 2022

First Posted (Actual)

November 7, 2022

Study Record Updates

Last Update Posted (Actual)

November 7, 2022

Last Update Submitted That Met QC Criteria

November 3, 2022

Last Verified

November 1, 2022

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)?

No

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

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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