Effects of Comedy Therapy on Pain and Comfort Levels in Liver Transplant Recipients
Principal Investigator, Assistant Professor Şerafettin OKUTAN, Surgical Nursing, Faculty of Health Sciences, Bitlis Eren University
1 other identifier
interventional
120
1 country
1
Brief Summary
This study was conducted to investigate the effects of watching excerpts from classical Turkish comedy films on pain and comfort levels in liver transplant recipients during the postoperative period. H1-0: Watching classical Turkish comedy films has no effect on postoperative pain in liver transplant recipients. H1-1: Watching classical Turkish comedy films reduces postoperative pain in liver transplant recipients. H2-0: Watching classical Turkish comedy films has no effect on postoperative comfort levels in liver transplant recipients. H2-1: Watching classical Turkish comedy films increases postoperative comfort levels in liver transplant recipients.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P50-P75 for not_applicable
Started Feb 2025
Shorter than P25 for not_applicable
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
First Submitted
Initial submission to the registry
January 31, 2025
CompletedFirst Posted
Study publicly available on registry
February 10, 2025
CompletedStudy Start
First participant enrolled
February 15, 2025
CompletedPrimary Completion
Last participant's last visit for primary outcome
September 25, 2025
CompletedStudy Completion
Last participant's last visit for all outcomes
October 7, 2025
CompletedDecember 4, 2025
November 1, 2025
7 months
January 31, 2025
November 27, 2025
Conditions
Keywords
Outcome Measures
Primary Outcomes (2)
pain level
Patients' pain level will be measured with a "numerical rating scale". In the form, 0 points are evaluated as "no pain", 1-3 points as "mild pain", 4-6 points as "moderate pain", 7 and above points as "severe pain".
It will take approximately 5 minutes
comfort level
General Comfort Scale: The general comfort scale was created by taking as a guide the taxonomic structure that includes three levels and four dimensions that constitute the theoretical components of comfort and is used to determine comfort requirements and to evaluate the situation of reaching the expected increase in comfort with nursing interventions that provide comfort. The scale is a four-point/six-point Likert type and contains a total of 48 items. The four-point Likert type was preferred in the study due to its ease of use. The lowest score that can be obtained from the scale is 48, the highest score is 192. High scores indicate a high level of comfort.
It will take approximately 30 minutes
Study Arms (2)
Intervention Group
EXPERIMENTALA patient introduction form, numerical rating scale and general comfort scale were applied as a pre-test after transplantation surgery. After patients came to the clinic after transplantation surgery and their condition was stable, 10-minute Turkish comedy films prepared by the researchers were shown. After the intervention, a numerical rating scale and general comfort scale were applied as a post-test. While patients watched the comedy films, a quiet and calm environment was provided in the patient room.
Control Group
NO INTERVENTIONA patient introduction form, numerical rating scale and general comfort scale were applied as a pre-test after transplantation surgery. No intervention was made to the control group patients outside of the clinical protocol. After patients came to the clinic after liver transplantation and their condition was stable, the numerical rating scale and general comfort scale were applied again.
Interventions
After patients came to the clinic after transplantation surgery and their condition was stable, 10-minute Turkish comedy films prepared by the researchers were shown.
Eligibility Criteria
You may qualify if:
- Being over 18 years of age,
- Being a liver transplant recipient,
- Data obtained after transplantation,
- Not having any visual or auditory problems.
You may not qualify if:
- Being under 18 years of age,
- Having any visual/auditory problems,
- Not accepting to participate in the study/wanting to leave,
- Not providing hemodynamic instability (sudden change in vital signs, etc.)
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
Bitlis Eren University
Bitlis, 13100, Turkey (Türkiye)
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Officials
- PRINCIPAL INVESTIGATOR
Şerafettin OKUTAN, Dr.
Study Principal Investigator Bitlis Eren University
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- NONE
- Purpose
- SUPPORTIVE CARE
- Intervention Model
- CROSSOVER
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Principal Investigator, Assistant Professor Şerafettin OKUTAN, Surgical Nursing, Faculty of Health Sciences, Bitlis Eren University
Study Record Dates
First Submitted
January 31, 2025
First Posted
February 10, 2025
Study Start
February 15, 2025
Primary Completion
September 25, 2025
Study Completion
October 7, 2025
Last Updated
December 4, 2025
Record last verified: 2025-11