The Effect of Laughter Yoga on Perceived Stress, Work Motivation, and Mental Well-Being

November 29, 2023 updated by: Celal Bayar University

The Effect of Laughter Yoga Applied to Intensive Care Nurses on Perceived Stress, Work Motivation, and Mental Well-Being

The aim of this randomized controlled experimental study is to examine the effect of laughter yoga applied to intensive care nurses on perceived stress, work motivation, and mental well-being.

Study Overview

Status

Completed

Detailed Description

The study was conducted with nurses working at Manisa Celal Bayar University Hospital's Surgical Intensive Care and Anesthesia Intensive Care units between December 2022 and March 2023. The Nurse Introduction Form, Nurse Work Motivation Scale, Perceived Stress Scale, and Warwick-Edinburgh Mental Well-being Scale were used to collect data.

Study Type

Interventional

Enrollment (Actual)

66

Phase

  • Not Applicable

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

    • MANİSAYunusemre
      • Manisa, MANİSAYunusemre, Turkey
        • Kivan Çevik Kaya

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

  • Adult

Accepts Healthy Volunteers

Yes

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

This section provides details of the study plan, including how the study is designed and what the study is measuring.

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

This is where you will find people and organizations involved with this study.

Investigators

  • Principal Investigator: Ramazan Yılmaz, Celal Bayar University

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

December 21, 2022

Primary Completion (Actual)

February 6, 2023

Study Completion (Actual)

March 1, 2023

Study Registration Dates

First Submitted

November 4, 2023

First Submitted That Met QC Criteria

November 29, 2023

First Posted (Actual)

December 8, 2023

Study Record Updates

Last Update Posted (Actual)

December 8, 2023

Last Update Submitted That Met QC Criteria

November 29, 2023

Last Verified

November 1, 2023

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)?

NO

IPD Plan Description

The data will be given if it's necessary and if it is not problem for ethical office.

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

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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