- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05129579
Psychological Resilience and Psychological Well-being of Intensive Care Nurses
The Effect of the Mindfulness Based Stress Reduction Intervention on Psychological Resilience and Psychological Well-being of Intensive Care Nurses
Purpose: This study aims to determine the impact of mindfulness-based stress reduction programs on the psychological resilience and well-being of intensive care nurses.
Design: The study was planned as an experimental study with a randomized control group, using pre-test, post-test and follow-up test.
Hypotheses: H1: The resilience level scores of the nurses in the intervention group participating in the mindfulness-based stress reduction initiative will increase compared to the nurses in the control group.
H2: Nurses in the intervention group participating in the mindfulness-based stress reduction initiative will increase their well-being level scores compared to the nurses in the control group.
H3: The psychological resilience level posttest and follow-up scores of the nurses in the intervention group participating in the mindfulness-based stress reduction initiative will increase compared to their pretest scores.
H4: The well-being level posttest and follow-up scores of the nurses in the intervention group participating in the mindfulness-based stress reduction initiative will increase according to their pretest scores.
Study Overview
Status
Conditions
Intervention / Treatment
Study Type
Enrollment (Anticipated)
Phase
- Not Applicable
Contacts and Locations
Study Contact
- Name: Merve Bat Tonkus, PhD Cand
- Phone Number: +905055951889
- Email: batmerve@gmail.com
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Description
Inclusion Criteria:
- Having Having a working time of at least 6 months in the intensive care unit,
- No barriers to accessing technology for participation in the online training program,
- Absence of a communication barrier related to vision and hearing
Exclusion Criteria:
- Working in the intensive care unit for less than 6 months
- Working in the intensive care unit due to temporary assignment
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Supportive Care
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
---|---|
Experimental: MBRSEG
The group in which the mindfulness-based stress reduction intervention will be implemented.
|
Mindfulness Based Stress Reduction intervention is a manualized course that includes meditation, relaxing movement, and breathing.
A certified MBSR instructor will teach the courses in a group-based format for 90 minute sessions, once per week for eight weeks.
|
Other: control group
The group to which mindfulness-based stress reduction intervention will not be applied
|
No intervention will be made in the control group.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Psychological Resilience Level
Time Frame: for 3 months
|
Psychological Resilience Scale for Adults: The scale consists of 33 items; it includes 6 sub-dimensions: The structural style (3,9,15,21) and perception of future (2,8,14,20) subdimensions were measured by 4 items each, the family cohesion (5,11,17,23,26,32), perception of self (1,7,13,19,28,31,), and social competence (4,10,16,22,25,29) sub-dimensions were measured by 6 items each, and the social resources (6,12,18,24,27,30,33) sub-dimension was measured by 7 items.
The score that can be obtained from the scale varies from 33 to 165.
|
for 3 months
|
Psychological Well-being Level
Time Frame: for 3 months
|
Psychological Well-Being Scale: The items of the scale are answered between 1 and 7, as I strongly disagree (1) and I strongly agree (7).
All items are expressed positively.
Scores range from 8 (strongly disagree to all items) to 56 (strongly agree to all items).
A high score indicates that the person has many psychological resources and strengths.
|
for 3 months
|
Collaborators and Investigators
Study record dates
Study Major Dates
Study Start (Anticipated)
Primary Completion (Anticipated)
Study Completion (Anticipated)
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
Keywords
Other Study ID Numbers
- IstanbulYeniYU
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
product manufactured in and exported from the U.S.
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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