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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT05606861
Other study ID # 69631334-300
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date November 20, 2018
Est. completion date January 30, 2019

Study information

Verified date November 2022
Source Ege University
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial 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.


Recruitment information / eligibility

Status Completed
Enrollment 29
Est. completion date January 30, 2019
Est. primary completion date December 28, 2018
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years to 58 Years
Eligibility 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 Design


Related Conditions & MeSH terms


Intervention

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

Locations

Country Name City State
Turkey Ege University Hospital Izmir

Sponsors (1)

Lead Sponsor Collaborator
Ege University

Country where clinical trial is conducted

Turkey, 

Outcome

Type Measure Description Time frame Safety issue
Primary Perceived Stress Level 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
Primary Psychological Resilience Level 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
Primary Empathy Level 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
Primary Self Compassion Level 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
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