- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06161623
The Effect of Laughter Yoga on Perceived Stress, Work Motivation, and Mental Well-Being
The Effect of Laughter Yoga Applied to Intensive Care Nurses on Perceived Stress, Work Motivation, and Mental Well-Being
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
-
-
MANİSAYunusemre
-
Manisa, MANİSAYunusemre, Turkey
- Kivan Çevik Kaya
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Adult
Accepts Healthy Volunteers
Description
Inclusion Criteria: Between 18-65 age
- Those who have worked as intensive care nurses for at least 6 months
- Those who agree to participate in the research
Exclusion Criteria:
- Those with chronic cough
- Those who have previously received laughter yoga training and practiced
- Those who had surgery within the last 3 months
- Those with diagnosed mental illness and those using medication (antidepressants, antipsychotics,anxiolytic, etc…)
- Those who have neurological diseases such as epilepsy and multiple sclerosis
- Those who have recently experienced a loss (within at least 6 months)
- Those with neurological disorders
- Those who have urinary incontinence problems
- Those who did not agree to participate in the research
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Supportive Care
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Single
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Laughter Yoga Application
The intervention group took eight sessions of laughter yoga, that is, two sessions per week for 4 weeks.
The participants in the intervention group were asked to fill in the data collection tools before the laughter yoga sessions, and after the 4th and 8th yoga sessions
|
The intervention group took eight sessions of laughter yoga, that is, two sessions per week for 4 weeks.
The participants in the intervention group were asked to fill in the data collection tools before the laughter yoga sessions, and after the 4th and 8th yoga sessions.
|
|
No Intervention: Control group
The participants in the control group also filled in the data collection tools without undergoing any intervention.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Work Motivation
Time Frame: 2 weeks
|
Work Motivation Scale was used. The highest score the scale can get in total is 75, while the lowest score is 25. High scale scores mean that nurses have high work motivation. |
2 weeks
|
|
Perceived Stress
Time Frame: 2 weeks
|
Perceived Stress Scale was used. A high total score on the scale indicates that the individual perceives high stress. High scores on the subscales are generally interpreted as negative. |
2 weeks
|
|
Mental Well-being
Time Frame: 2 weeks
|
Warwick-Edinburgh Mental Well-being Scale was used. It can score between a minimum of 14 and a maximum of 70 points. High scores indicate that the individual is in a good psychological state. |
2 weeks
|
Collaborators and Investigators
Sponsor
Investigators
- Principal Investigator: Ramazan Yılmaz, Celal Bayar University
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
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
Other Study ID Numbers
- MCBU-K-CEVIK-002
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
IPD Plan Description
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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