- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05717231
The Effect of Laughter Yoga on Tex Anxiety and Educational Stress
January 29, 2023 updated by: Bilge Kalanlar, Hacettepe University
The Effect of Laughter Yoga on Tex Anxiety and Educational Stress in 8th-Grade Students
The primary purpose of this study is to examine the effects of laughter therapy on tex anxiety and educational stress in 8th-grade students.
Study Overview
Status
Completed
Conditions
Intervention / Treatment
Study Type
Interventional
Enrollment (Actual)
64
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
-
-
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Ankara, Turkey
- Bilge KALANLAR
-
-
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
13 years to 14 years (CHILD)
Accepts Healthy Volunteers
Yes
Genders Eligible for Study
All
Description
The inclusion criteria of the study were determined as being an 8th-grade student, speaking and understanding Turkish, and being able to perform daily life activities.
The exclusion criteria of the study were to have undergone a surgical operation in the last three months, and to have uncontrollable blood pressure, diabetes and asthma.
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
- Masking: DOUBLE
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
---|---|
EXPERIMENTAL: laughter yoga
Laughter yoga was performed face-to-face with the intervention group for 35-40 minutes twice a week and in 6 sessions in total.
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laughter yoga
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NO_INTERVENTION: Control group
No intervention was performed for the control group
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Westside Test Anxiety Scale
Time Frame: up to 6 weeks
|
The Westside Test Anxiety Inventory is a ten-item scale in a single dimension that aims to measure test anxiety.
The scale was developed to be used in examining the effect of a program to reduce test anxiety.
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up to 6 weeks
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Educational stress
Time Frame: up to 6 weeks
|
It is a self-reported 5-point Likert-type measurement tool consisting of 16 items.
The educational stress scale consists of four sub-dimensions: work pressure, course load, success anxiety, and expectation versus hopelessness.
In addition to the sub-dimensions in the scale, the total score for the overall scale is calculated.
|
up to 6 weeks
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
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)
April 3, 2022
Primary Completion (ACTUAL)
June 9, 2022
Study Completion (ACTUAL)
June 9, 2022
Study Registration Dates
First Submitted
January 29, 2023
First Submitted That Met QC Criteria
January 29, 2023
First Posted (ACTUAL)
February 8, 2023
Study Record Updates
Last Update Posted (ACTUAL)
February 8, 2023
Last Update Submitted That Met QC Criteria
January 29, 2023
Last Verified
January 1, 2023
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- E2273
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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