Effect of Laughter Yoga on Nursing Students

December 8, 2023 updated by: Olga Incesu, Istanbul University - Cerrahpasa (IUC)

The Effect of Laughter Yoga on Nursing Students' Well-Being, Perceived Stress and Academic Self-Efficacy: A Randomised Controlled Study

Nursing students experience different levels of stress due to many reasons such as lifestyle, health, academic performance, competition, choice of profession, new living environment, relationships with peer group and expectations of parents. It is important to develop different coping behaviours/strategies to manage stressful situations. Laughter yoga has proven positive effects on physical and mental health.

The aim of this randomised controlled trial was to examine the effects of laughter yoga on well-being, perceived stress and academic self-efficacy of nursing students.

Study Overview

Status

Recruiting

Intervention / Treatment

Detailed Description

Laughter yoga, which is a combination of laughter and yoga with breathing techniques, is among traditional and complementary medicine practices. Based on the view that the brain cannot distinguish between real and unreal laughter, laughter yoga aims to benefit from the mental and physical benefits of laughter. Laughter yoga has benefits such as reducing stress and depression symptoms, relaxing muscle tone, increasing blood circulation, lowering blood pressure, increasing melatonin and growth hormone release, increasing pain threshold, strengthening the immune system.

Laughter yoga will be applied to the intervention group in 6 sessions (45 minutes each session). Well-being, Perceived Stress and Academic Self-Efficacy levels of the students will be evaluated before and after the intervention.

Hypotheses of the study; H1: The well-being level of the intervention group increases after laughter yoga.

H2: The academic self-efficacy level of the intervention group increases after laughter yoga.

H3: Perceived stress level of the intervention group decreases after laughter yoga.

H4: The well-being level of the intervention group after laughter yoga is higher than the control group.

H5: The perceived stress level of the intervention group after laughter yoga is lower than the control group.

H6: The academic self-efficacy level of the intervention group after laughter yoga is higher than the control group.

Study Type

Interventional

Enrollment (Estimated)

80

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 Contact

Study Contact Backup

Study Locations

    • Şişli
      • Istanbul, Şişli, Turkey, 34381
        • Recruiting
        • Olga İncesu
        • Contact:

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:

  • To be a 4th year nursing student,
  • Volunteer to participate

Exclusion Criteria:

  • To take part in the intern programme,
  • Simultaneous participation in any methods of complementary medicine,
  • Having undergone surgery within the last three months,
  • Having a diagnosis of hernia (hernia)
  • Having a diagnosis of epilepsy
  • Uncontrolled diabetes and cardiovascular disease

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: Single

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Experimental: Laughter yoga group
Laughter yoga will be applied to the intervention group in 6 sessions (45 minutes each session). Laughter yoga consists of four parts. Firstly, it starts with warm-up exercises including hand clapping (applause), singing "ho ho ha ha" to relax the facial muscles of the participants and body movements. Secondly, the lungs are prepared with breathing exercises and the mind is prepared for laughter with childish games. This is followed by laughter exercises. Deep breathing exercises are performed between laughter exercises. Laughter yoga is concluded with clapping, singing and relaxation exercises.
Laughter yoga will be applied to the intervention group in 6 sessions (45 minutes each session).
No Intervention: Control group
No laughter yoga intervention will be applied to the control group.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Well being
Time Frame: 2 weeks post intervention
The WHO-5 well-being Scale point of the intervention group change laughter yoga.
2 weeks post intervention
Academic self-efficcay
Time Frame: 2 weeks post intervention
The academic self-efficacy point of the intervention group change after laughter yoga.
2 weeks post intervention
Stress
Time Frame: 2 weeks post intervention
The perceived stress scale point of the intervention group change after laughter yoga.
2 weeks post intervention

Collaborators and Investigators

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

Investigators

  • Study Director: Merve Altıner Yaş, Dr, Dr

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)

October 16, 2023

Primary Completion (Actual)

November 29, 2023

Study Completion (Estimated)

December 30, 2023

Study Registration Dates

First Submitted

November 29, 2023

First Submitted That Met QC Criteria

December 8, 2023

First Posted (Actual)

December 19, 2023

Study Record Updates

Last Update Posted (Actual)

December 19, 2023

Last Update Submitted That Met QC Criteria

December 8, 2023

Last Verified

December 1, 2023

More Information

Terms related to this study

Other Study ID Numbers

  • Florence Nightingale Faculty-3

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

NO

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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