- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06071169
The Effect of Progressive Relaxation Exercise on Nurses
The Effect of Progressive Relaxation Exercise on Nurses' Life Satisfaction, Comfort and Burnout Levels
Study Overview
Status
Intervention / Treatment
Detailed Description
Study Type
Enrollment (Estimated)
Phase
- Not Applicable
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Adult
- Older Adult
Accepts Healthy Volunteers
Description
Inclusion Criteria:
Working as a nurse in a tertiary treatment center for at least 3 years Have not participated in any relaxation exercise Absence of neurological/psychiatric disorders Not having an obstacle to exercise Nurses who volunteered to participate in the study will be included in the study.
Exclusion Criteria:
Individuals who have any exercise program and use any relaxation method (yoga, acupuncture, massage, music therapy, etc.) will not be included in the study.
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: Intervention
progressive relaxation exercise group The nurses will perform the relaxation exercises 3 days a week for 5 weeks, 20 minutes in each practice.
|
Nurses will be asked to perform relaxation exercises 3 days a week for 5 weeks, 20 minutes in each practice.
|
No Intervention: Control
Control group No application has been made.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Comfort
Time Frame: 5 weeks after first meeting
|
The scale consists of 39 items in total.
Each statement in the scale has a Likert-type rating ranging from 1-4 from "strongly disagree" to "strongly agree".
24 of the expressions are positive and 15 are negative, and negative items are reversed in scoring.
Accordingly, a high score (4) indicates high comfort, a low score (1) indicates low comfort, and a low score (1) indicates high comfort in negative statements, and a high score (4) indicates low comfort.
The Cronbach alpha coefficient was found to be 0.915.
|
5 weeks after first meeting
|
Satisfaction with Life
Time Frame: 5 weeks after first meeting
|
It was developed to determine an individual's satisfaction with his/her life.
The scale consists of five Likert-style items on a 7-point scale (1: strongly disagree, 7: strongly agree).
The lowest score that can be obtained from the scale is 5 and the highest score is 35.
A low score is accepted as an indicator of low life satisfaction and a high score as an indicator of high life satisfaction.
|
5 weeks after first meeting
|
Burnout
Time Frame: 5 weeks after first meeting
|
It was created to measure the perceived burnout level.
The scale consists of 22 items in total and is 7-point Likert type.
These options are as follows in terms of severity; 1- Never, 2- Very Rarely, 3- Sometimes, 4- Most of the Time, 5- Always.
There are three subscales: emotional exhaustion, depersonalization and low personal accomplishment.
|
5 weeks after first meeting
|
Collaborators and Investigators
Sponsor
Study record dates
Study Major Dates
Study Start (Estimated)
Primary Completion (Estimated)
Study Completion (Estimated)
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
Additional Relevant MeSH Terms
Other Study ID Numbers
- 47/2023
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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