The Effect of Laughter Yoga on Mindfulness, Proffessional Resilience and Self-Care

May 14, 2025 updated by: Nuriye Yıldırım, Duzce University

The Effect of Laughter Yoga as a Nursing Intervention on Nurses' Mindfulness, Proffessional Resilience and Self-Care

The aim of this study was to evaluate the effect of laughter yoga on mindfulness, professional resilience and self-care among nurses. The hypotheses of the study suggested that laughter yoga would have an effect on mindfulness, professional resilience and self-care scores among nurses.

Study Overview

Status

Completed

Intervention / Treatment

Detailed Description

Laughter yoga is an independent nursing intervention that includes breathing and laughter exercises. Studies have proven that laughter yoga decreases stress hormones, increases hormones such as endorphins, decreases leukocytes and provides protection against infection, accelerates circulation, increases pain tolerance and quality of life, decreases blood pressure, stress, anxiety and tension, improves mental well-being and self-esteem, improves memory and creative thinking skills, and strengthens interpersonal communication. Many of these studies have been conducted in patients, healthy adults, the elderly, nursing and university students. There are a limited number of studies in which laughter yoga was applied as an intervention in a sample of nurses. In the studies, it was determined that laughter yoga decreased cortisol hormone, fatigue levels, perceived stress, burnout levels, increased life satisfaction, attention levels and individual work performance, psychological resilience and sleep quality in nurses.

Purpose: The aim of this study was to evaluate the effect of laughter yoga on mindfulness, professional resilience and self-care among nurses.

Method:

The study is planned as an experimental research with a randomized controlled pretest-posttest control group. This study is planned to be conducted in Düzce Atatürk State Hospital between February 2024 and December 2024.

The sample size for the study was calculated using the G*Power 3.1.9.7 program. There was no article that could be taken as a reference for the scales included in this study. Therefore, taking a medium effect level (d=0.5), 5% margin of error (α=0.05), 80% power (1β=0.80) and 1:2 intervention-control group ratio, the number of people who should be included in the study according to the one-way hypothesis was found as 38 participants for the intervention group and 76 participants for the control group. Assuming drop outs, the sample size will be determined as 40 participants for the experimental group and 80 participants for the control group.

The data will be collected through "Personal Information Form", "Five Dimensional Mindfulness Scale", "Skovholt Professional Resilience and Self-Care Inventory" and "Post Laughter Yoga Evaluation Form

Study Type

Interventional

Enrollment (Actual)

72

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

    • Merkez
      • Düzce, Merkez, Turkey, 81620
        • Düzce Üniversitesi

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
  • Older Adult

Accepts Healthy Volunteers

Yes

Description

Inclusion Criteria:

  • Volunteering to participate in the study
  • Working as a nurse at Düzce Atatürk State Hospital
  • Not doing laughter yoga before

Exclusion Criteria:

  • Currently being in the process of any psychiatric treatment or psychotherapy

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: Other
  • Allocation: Randomized
  • Interventional Model: Parallel Assignment
  • Masking: Double

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Experimental: Interventional group / Laughter yoga

The data of the pre-intervention study will be recorded with "Personal Information Form", "Five Dimensional Mindfulness Scale" and "Skovholt Professional Resilience and Self-Care Inventory".

The application will be done for 8 weeks, 1 day a week. Post-intervention data will be collected with "Five Dimensional Mindfulness Scale" and "Skovholt Professional Resilience and Self-Care Inventory" and "Post Laughter Yoga Evaluation Form".

In Laughter Yoga Practice; each session will last approximately 30 - 45 minutes and will consist of four parts. These parts are: warm-up exercises, deep breathing exercises, childlike games and laughter exercises.
Other Names:
  • Interventional group
No Intervention: Control group
The control group did not take part in the laughter yoga program. As a pre-test, the data of the study will be recorded with "Personal Information Form", "Five Dimensional Mindfulness Scale" and "Skovholt Professional Resilience and Self-Care Inventory". As the post-test, 8 weeks after the pre-test, the data of the study will be collected with the "Five Dimensional Mindfulness Scale" and "Skovholt Professional Resilience and Self-Care Inventory".

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Five Dimensional Mindfulness Scale Scores
Time Frame: Up to 8 weeks
The Five Dimensional Mindfulness Scale developed by Baer et al. (2008), whose Turkish validity and reliability was studied by Kınay F. (2013), has 5 sub-dimensions: Acting with awareness, Identification, Observation, Not judging inner experiences, and non-reactivity to inner experiences. The scale is a 5-point Likert scale consisting of 39 questions. The internal consistency coefficient of the original scale varies between 0.75-0.91. There is no reference point in the GCBFQ. The higher the value at the end of the scale, the higher the level of mindfulness.
Up to 8 weeks

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Skovholt Professional Resilience and Self-Care Inventory Scores
Time Frame: up to 8 weeks
The Turkish validity and reliability of Skovholt Professional Resilience and Self-Care Inventory developed by Skovholt (2012) was studied by Güneri et al (2017). The scale has 4 sub-dimensions: Professional wellness, Personal wellness, Professional stress and Personal stress. The scale is a 5-point Likert scale consisting of 38 questions. The total score range of the scale varies between 38 and 190, with all items being positive. High scores obtained from the scale indicate high professional resilience. The reliability coefficient of the scale was found to be 0.92.
up to 8 weeks

Collaborators and Investigators

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

Collaborators

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)

May 14, 2024

Primary Completion (Actual)

May 1, 2025

Study Completion (Actual)

May 14, 2025

Study Registration Dates

First Submitted

January 11, 2024

First Submitted That Met QC Criteria

January 11, 2024

First Posted (Actual)

January 22, 2024

Study Record Updates

Last Update Posted (Actual)

May 15, 2025

Last Update Submitted That Met QC Criteria

May 14, 2025

Last Verified

May 1, 2025

More Information

Terms related to this study

Other Study ID Numbers

  • DuzceU-SBF-NYS-01

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

product manufactured in and exported from the U.S.

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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