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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
Full 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.
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60 participants in 2 patient groups
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Data sourced from clinicaltrials.gov
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