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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT05681013
Other study ID # 739904
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date February 1, 2021
Est. completion date June 17, 2022

Study information

Verified date December 2022
Source Mugla Sitki Koçman University
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The aim of this study is to determine the effect of laughter therapy on the general health status, sleep quality, and stress level of nursing students.


Description:

H1.1: Students who receive laughter therapy will have lower mean scores in the general health questionnaire than students who do not receive laughter therapy. H1.2: Students who receive laughter therapy will have a lower Pittsburgh sleep quality index score than students who do not receive laughter therapy. H1.3: Students who receive laughter therapy will have a lower mean stress level than students who do not receive laughter therapy.


Recruitment information / eligibility

Status Completed
Enrollment 70
Est. completion date June 17, 2022
Est. primary completion date May 30, 2021
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years to 23 Years
Eligibility Inclusion Criteria: - Volunteering to participate in research - Being a 1st or 2nd-year student in the Faculty of Health Sciences, Department of Nursing - Not have any health problems that may create a communication barrier - Being in a quiet environment to participate in the online study due to the pandemic period - Have an internet connection to attend online sessions Exclusion Criteria: - Having undergone abdominal surgery in the past three months - Having a disability to attend regular sessions

Study Design


Intervention

Behavioral:
Laughter Therapy
The effect of the Laughter Therapy on nursing students

Locations

Country Name City State
Turkey Mugla Sitki Koçman University Mugla

Sponsors (1)

Lead Sponsor Collaborator
Mugla Sitki Koçman University

Country where clinical trial is conducted

Turkey, 

Outcome

Type Measure Description Time frame Safety issue
Primary Introductory Information Form It was prepared by the researchers in line with the literature in order to collect data about the individual characteristics of the participants. Form; family structure, gender, income status, marital status, health status, age, etc. It consists of 13 items (pretest-posttest design was applied). 2 minutes
Primary General Health Questionnaire-28 (GHQ-28) It was prepared to detect mental health problems. Individuals who score below 5 on the scale are evaluated as "normal", while individuals who score 5 and above are considered as a "risk group" in terms of mental health (pretest-posttest design was applied). 5 minutes
Primary Pittsburgh Sleep Quality Index (PUKI) "Poor sleep quality" is expressed for individuals who score 5 and above from the scale. The scale consists of 24 items that evaluate sleep quality and disorders by scoring over a one-month period (pretest-posttest design was applied). 5 minutes
Primary Perceived Stress Scale (PSS) The scale, which was prepared to evaluate the perceived stress level of the individual, consists of 14 items. High scores obtained from the scale indicate that the person has a high perception of stress(pretest-posttest design was applied). 3 minutes
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