NCT06816628

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

87
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
120

participants targeted

Target at P50-P75 for not_applicable

Timeline
Completed

Started Feb 2025

Shorter than P25 for not_applicable

Geographic Reach
1 country

1 active site

Status
completed

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

Completed
10 days until next milestone

First Posted

Study publicly available on registry

February 10, 2025

Completed
5 days until next milestone

Study Start

First participant enrolled

February 15, 2025

Completed
7 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

September 25, 2025

Completed
12 days until next milestone

Study Completion

Last participant's last visit for all outcomes

October 7, 2025

Completed
Last Updated

December 4, 2025

Status Verified

November 1, 2025

Enrollment Period

7 months

First QC Date

January 31, 2025

Last Update Submit

November 27, 2025

Conditions

Keywords

paincomforttransplantliverpost-operatif

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

EXPERIMENTAL

A 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.

Other: comedy therapy

Control Group

NO INTERVENTION

A 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.

Intervention Group

Eligibility Criteria

Age18 Years+
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64), Older Adult (65+)

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)

Location

MeSH Terms

Conditions

Pain, PostoperativePatient Acceptance of Health CarePain

Condition Hierarchy (Ancestors)

Postoperative ComplicationsPathologic ProcessesPathological Conditions, Signs and SymptomsNeurologic ManifestationsSigns and SymptomsTreatment Adherence and ComplianceHealth BehaviorBehavior

Study Officials

  • Şerafettin OKUTAN, Dr.

    Study Principal Investigator Bitlis Eren University

    PRINCIPAL INVESTIGATOR

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
NONE
Purpose
SUPPORTIVE CARE
Intervention Model
CROSSOVER
Model Details: It will be conducted as a randomized controlled experimental study in a pre-testpost- test control group experimental model.
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

Locations