PRoNMBSR: Mindfulness Based Interventions in Pediatric Nurses

Sponsor
Ege University (Other)
Overall Status
Completed
CT.gov ID
NCT05606861
Collaborator
(none)
29
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2
2.3
12.4

Study Details

Study Description

Brief Summary

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.

Condition or Disease Intervention/Treatment Phase
  • Other: Mindfulness Based Interventions in Pediatric Nurses
N/A

Study Design

Study Type:
Interventional
Actual Enrollment :
29 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
Double (Participant, Outcomes Assessor)
Primary Purpose:
Prevention
Official Title:
Effect of Mindfulness Based Stres Reduction Intervention on Psychological Resilience of Child Nurses: Randomized Controlled Trial
Actual Study Start Date :
Nov 20, 2018
Actual Primary Completion Date :
Dec 28, 2018
Actual Study Completion Date :
Jan 30, 2019

Arms and Interventions

Arm Intervention/Treatment
Experimental: Intervention group

Mindfulness Based Intervention in pediatric nurses components was applied to this group.

Other: Mindfulness Based Interventions in Pediatric Nurses
This intervention are structured mindfulness program including meditation and breathing techniques .

No Intervention: Control group

No procedure was conducted the control group.

Outcome Measures

Primary Outcome Measures

  1. Perceived Stress Level [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.

  2. Psychological Resilience Level [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.

  3. Empathy Level [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.

  4. Self Compassion Level [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.

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years to 58 Years
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
Yes
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.

Contacts and Locations

Locations

Site City State Country Postal Code
1 Ege University Hospital İzmir Turkey 35100

Sponsors and Collaborators

  • Ege University

Investigators

None specified.

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Tülün Liman, Principal investigator, Ege University
ClinicalTrials.gov Identifier:
NCT05606861
Other Study ID Numbers:
  • 69631334-300
First Posted:
Nov 7, 2022
Last Update Posted:
Nov 7, 2022
Last Verified:
Nov 1, 2022
Individual Participant Data (IPD) Sharing Statement:
No
Plan to Share IPD:
No
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Keywords provided by Tülün Liman, Principal investigator, Ege University

Study Results

No Results Posted as of Nov 7, 2022