The Effect of Laughter Yoga on Spiritual Care Perception and Spiritual Well Being in Nursing Students

July 11, 2025 updated by: Begüm Güler, Izmir Democracy University

Can Laughter Heal the Spirit? The Impact of Laughter Yoga on Spiritual Well-Being and Spiritual Care Perception in Nursing Students

The goal of this clinical trial is to learn if laughter yoga sessions improve spiritual well-being and perception of spiritual care among nursing students. The main questions it aims to answer are:

Does laughter yoga increase the spiritual well-being scores of participants? Does laughter yoga improve participants' perception of spiritual care? Researchers will compare laughter yoga to no intervention (control group) to see if laughter yoga has an effect on spiritual well-being and spiritual care perception.

Participants will:

Attend laughter yoga sessions once a week for 4 weeks (intervention group) Complete questionnaires about their spiritual well-being and perception of spiritual care before and after the intervention Control group will not receive any intervention during this period, but will complete the same questionnaires at the same time points

Study Overview

Status

Completed

Intervention / Treatment

Detailed Description

This randomized controlled trial aims to evaluate the effects of laughter yoga on spiritual well-being and perception of spiritual care among nursing students. The study uses a pretest-posttest control group design. A total of 60 nursing students in their third and fourth years were randomly assigned to either the intervention group or the control group, with 30 students in each group.

The intervention group will participate in laughter yoga sessions once a week for 4 weeks. Each session will last approximately 30 minutes and will be conducted by a certified laughter yoga leader in a quiet classroom environment where students can move freely. The control group will not receive any intervention during the study period.

Spiritual well-being will be measured using the Spiritual Well-Being Scale (SWBS) and perception of spiritual care will be measured using the Spiritual Care-Giving Scale (SCGS). Both scales will be administered before the intervention (pretest) and after the 4-week intervention period (posttest).

The study hypothesizes that laughter yoga will significantly increase spiritual well-being scores and improve students' perception of spiritual care compared to the control group.

Study Type

Interventional

Enrollment (Actual)

60

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

    • Konak
      • Izmir, Konak, Turkey, 35250
        • Izmir Democracy University

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

  • Child
  • Adult
  • Older Adult

Accepts Healthy Volunteers

Yes

Description

Inclusion Criteria:

  • Being a third- or fourth-year nursing student enrolled in the Faculty of Health Sciences, Department of Nursing at Izmir Demokrasi University during the 2024-2025 academic year
  • Volunteering to participate in the study

Exclusion Criteria:

  • Irregular attendance to the intervention sessions
  • Failure to complete all sessions
  • Voluntary withdrawal from the study
  • Having a diagnosis of a respiratory disease (e.g., asthma, bronchitis, dyspnea)
  • Having a diagnosis of inguinal hernia or epilepsy
  • Having undergone abdominal surgery within the last three to six months

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 Intervention
Participants in this arm will attend laughter yoga sessions once a week for 4 weeks. Each session will last approximately 30 minutes and will be conducted by a certified laughter yoga leader in a quiet classroom environment where participants can move freely. The intervention aims to improve spiritual well-being and perception of spiritual care among nursing students.

The laughter yoga intervention consists of four sessions conducted once a week for four weeks. Each session lasts approximately 30 minutes and includes four components:

  • Warm-up exercises with clapping and rhythmic movements
  • Deep breathing exercises
  • Childlike playful activities and laughter exercises
  • Laughter meditation and relaxation Sessions are led by a certified laughter yoga leader in a quiet classroom setting that allows participants to move freely and comfortably. The intervention is designed to improve spiritual well-being and perception of spiritual care among nursing students.
No Intervention: Control Group
Participants in this arm will not receive any intervention during the 4-week study period. They will complete the same pretest and posttest questionnaires as the intervention group, at the same time points, to evaluate their spiritual well-being and perception of spiritual care.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Change in Spiritual Well-Being Score
Time Frame: 1 week before intervention (baseline) and 1 week after completing the fourth session (Week 5)
Spiritual well-being will be measured using the Three-Factor Spiritual Well-Being Scale, which has a total score range from 29 to 145, with higher scores indicating greater spiritual well-being.
1 week before intervention (baseline) and 1 week after completing the fourth session (Week 5)

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Change in Spirituality and Spiritual Care Rating Scale Score
Time Frame: 1 week before intervention (baseline) and 1 week after completing the fourth session (Week 5)
Perception of spirituality and spiritual care will be assessed using the Spirituality and Spiritual Care Rating Scale, which is scored on a 1 to 5 scale, with higher scores indicating a more positive perception of spirituality and spiritual care.
1 week before intervention (baseline) and 1 week after completing the fourth session (Week 5)

Collaborators and Investigators

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

Investigators

  • Study Director: Sadiye Associate Professor, PhD, Izmir Democracy 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)

September 20, 2024

Primary Completion (Actual)

October 21, 2024

Study Completion (Actual)

November 25, 2024

Study Registration Dates

First Submitted

July 2, 2025

First Submitted That Met QC Criteria

July 11, 2025

First Posted (Actual)

July 14, 2025

Study Record Updates

Last Update Posted (Actual)

July 14, 2025

Last Update Submitted That Met QC Criteria

July 11, 2025

Last Verified

July 1, 2025

More Information

Terms related to this study

Other Study ID Numbers

  • 2024/6-20

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

NO

IPD Plan Description

Individual participant data (IPD) will not be shared because the data are part of a thesis study with limited scope and there is no current plan or institutional repository available for data sharing. Additionally, participant privacy and confidentiality cannot be ensured for sharing de-identified data at this time.

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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