The Effect of Laughter Therapy on Nursing Students

Sponsor
Muğla Sıtkı Koçman University (Other)
Overall Status
Completed
CT.gov ID
NCT05681013
Collaborator
(none)
70
1
2
16.5
4.3

Study Details

Study Description

Brief 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.

Condition or Disease Intervention/Treatment Phase
  • Behavioral: Laughter Therapy
N/A

Detailed 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.

Study Design

Study Type:
Interventional
Actual Enrollment :
70 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
Double (Participant, Outcomes Assessor)
Primary Purpose:
Supportive Care
Official Title:
The Effect of Laughter Therapy on the General Health Status, Sleep Quality, and Stress Level of Nursing Students
Actual Study Start Date :
Feb 1, 2021
Actual Primary Completion Date :
May 30, 2021
Actual Study Completion Date :
Jun 17, 2022

Arms and Interventions

Arm Intervention/Treatment
Experimental: Laughter Therapy Group

A pre-test was administered to all students. In the pre-test application, the Descriptive Information Form, General Health Questionnaire-28, Pittsburgh Sleep Quality Index and Perceived Stress Scale were applied. Experimental and control groups were formed randomly among the students who filled all the scales. Communication groups were established for the students in both groups without being told which group they belonged to. Considering the hours suitable for the experimental group, 8 sessions of laughter therapy were applied for an average of 45 minutes. At the end of the therapy in the last session, a post-test was administered to all of the students. In the post-test application, the Descriptive Information Form, General Health Questionnaire-28, Pittsburgh Sleep Quality Index, and Perceived Stress Scale were applied.

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

No Intervention: Control Group

In the pre-test application, the Descriptive Information Form, General Health Questionnaire-28, Pittsburgh Sleep Quality Index, and Perceived Stress Scale were applied. At the end of the therapy in the last session, a post-test was administered to all students. In the post-test application, the Descriptive Information Form, General Health Questionnaire-28, Pittsburgh Sleep Quality Index, and Perceived Stress Scale were applied.

Outcome Measures

Primary Outcome Measures

  1. Introductory Information Form [2 minutes]

    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. General Health Questionnaire-28 (GHQ-28) [5 minutes]

    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).

  3. Pittsburgh Sleep Quality Index (PUKI) [5 minutes]

    "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).

  4. Perceived Stress Scale (PSS) [3 minutes]

    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).

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years to 23 Years
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
Yes
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

Contacts and Locations

Locations

Site City State Country Postal Code
1 Muğla Sıtkı Koçman University Mugla Turkey

Sponsors and Collaborators

  • Muğla Sıtkı Koçman University

Investigators

  • Principal Investigator: Elif Uner, Dr, Muğla Sıtkı Koçman University

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Elif Uner, Assistant Professor, Muğla Sıtkı Koçman University
ClinicalTrials.gov Identifier:
NCT05681013
Other Study ID Numbers:
  • 739904
First Posted:
Jan 11, 2023
Last Update Posted:
Jan 11, 2023
Last Verified:
Dec 1, 2022
Individual Participant Data (IPD) Sharing Statement:
No
Plan to Share IPD:
No
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Keywords provided by Elif Uner, Assistant Professor, Muğla Sıtkı Koçman University
Additional relevant MeSH terms:

Study Results

No Results Posted as of Jan 11, 2023