- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT07062029
- Original Trial
The Effect of Laughter Yoga on Spiritual Care Perception and Spiritual Well Being in Nursing Students
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
Conditions
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
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
-
-
Konak
-
Izmir, Konak, Turkey, 35250
- Izmir Democracy University
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Child
- Adult
- Older Adult
Accepts Healthy Volunteers
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
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:
|
|
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
Sponsor
Investigators
- Study Director: Sadiye Associate Professor, PhD, Izmir Democracy 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
- 2024/6-20
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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