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The Effect of Children's Laughter Video on Oncology Patient

The Impact of Children Laughter Intervention on Anxiety, Nausea, Vomiting, and Fatigue in Chemotherapy Patients - A Randomized Controlled Trial

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT07051616
Enrollment
36
Registered
2025-07-04
Start date
2023-09-15
Completion date
2025-05-30
Last updated
2025-07-04

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Anxiety, Chemotherapy Effect, Fatigue, Laughter, Nausea, Vomiting

Brief summary

This study was conducted to investigate the effect of video playback of children's laughter on anxiety, nausea, vomiting and fatigue levels of patients during chemotherapy

Detailed description

Nausea and vomiting, anxiety and fatigue due to chemotherapy can be prevented or reduced with effective nursing interventions and care. Laughter therapy is an intervention that has been used in the symptom management of individuals with cancer in recent years. Studies focusing on humor and laughter have generally been conducted among cancer patients. Humor and laughter have been shown to have both physiological, psychological and sociological benefits for patients in general. When the studies on laughter yoga are examined, it is seen that the results of laughter therapy applied to individuals are examined. It has also been reported in the literature that laughter has a contagious effect, often occurring in groups of people. There is no study in the literature on the effect of children's laughter on adults. This study will reveal the effectiveness of infant and child laughter in patients receiving chemotherapy. It is thought that this study will constitute an important data source for experimental studies to be conducted.

Interventions

BEHAVIORALChild laughter video

1 hour after the chemotherapy treatment was started, the video monitor was placed at a height where the patient could see comfortably while lying down and the video, which was checked and prepared beforehand, was turned on full screen. The appropriate volume was adjusted and the patient was allowed to watch the video for 10 minutes without any other intervention. The video was then stopped and the etagere was removed from in front of the patient. Chemotherapy was continued. At the 2nd hour of chemotherapy, the disinfected etagere and computer were placed in a position where the patient could see them comfortably and the 2nd video was started and the patient was allowed to watch the video for 10 minutes.

Sponsors

Selcuk University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
SUPPORTIVE_CARE
Masking
SINGLE (Subject)

Eligibility

Sex/Gender
ALL
Age
32 Years to 81 Years
Healthy volunteers
No

Inclusion criteria

* Diagnosed with lymphoma (preferred to have the same type of cancer) * Receiving the R - Chop cycle protocol as chemotherapy (This cycle was preferred because of the nausea and vomiting experienced in this protocol and the duration of the treatment is 4-5 hours) (Cleveland Clinic 2025). * Inpatient hospitalization, * Be over 18 years of age, * Conscious, oriented and cooperative

Exclusion criteria

* Don't take a different cure than R - Chop, * Visual and hearing and cognitive impairment, * Do not have a problem that creates a communication barrier, * Having any psychiatric illness such as depression, euphoria and taking psychiatric medication * Refusal to participate in the study * Other non-pharmacological methods

Design outcomes

Primary

MeasureTime frameDescription
Vomiting Follow-up FormAs soon as chemotherapy is started (Within first five minute)With this form, the presence or absence of the patient's vomiting was questioned. Vomiting was first measured at the start of chemotherapy
FACIT Fatigue ScaleFirst measurement- 1 minutes before the start of the patient's chemotherapyDeveloped by Singh in 2014, the scale was developed to evaluate the relationship between anemia and fatigue in cancer patients and to meet the increasing demand. This form was applied in the pre-test and post-test phase.
Physiological Parameter Follow-up Form (Heart rate-min)As soon as chemotherapy is started (Within first five minute)This form was created by researchers. When chemotherapy started and measured at the beginning of each hour.
Physiological Parameter Follow-up Form (Respiration rate- min)As soon as chemotherapy is started (Within first five minute)This form was created by researchers. When chemotherapy started and measured at the beginning of each hour.
Physiological Parameter Follow-up Form (oxygen saturation -SpO2%)As soon as chemotherapy is started (Within first five minute)This form was created by researchers. When chemotherapy started and measured at the beginning of each hour.
Physiological Parameter Follow-up Form (blood pressure- mmHg)As soon as chemotherapy is started (Within first five minute)This form was created by researchers. When chemotherapy started and measured at the beginning of each hour.
Nausea Follow-up FormAs soon as chemotherapy is started (Within first five minute)With this form, the presence or absence of the patient's nause was questioned.Nausea was first measured at the start of chemotherapy
Patient information formFirst measurement-10. minutes before the start of the patient's chemotherapyThe form was designed by the researchers in two parts to assess personal characteristics and characteristics related to the disease and treatment.
Spielberger State Anxiety ScaleFirst measurement- 5 minutes before the start of the patient's chemotherapyThe scale measures the level of status anxiety of the patient with 20 questions.this form was applied in the pre-test and post-test phase

Secondary

MeasureTime frameDescription
Physiological Parameter Follow-up Form (Respiration rate- min)Second measurement: 1. hour after starting chemotherapyThe measurement was made immediately after the first hour was full.
Physiological Parameter Follow-up Form (oxygen saturation -SpO2%)Second measurement: 1. hour after starting chemotherapyThe measurement was made immediately after the first hour was full.
Physiological Parameter Follow-up Form (blood pressure- mmHg)Second measurement: 1. hour after starting chemotherapyThe measurement was made immediately after the first hour was full.
Nausea Follow-up FormSecond measurement: 1. hour after starting chemotherapyThe measurement was made immediately after the first hour was full.
Vomiting Follow-up FormSecond measurement: 1. hour after starting chemotherapyThe measurement was made immediately after the first hour was full.
Physiological Parameter Follow-up Form (Heart rate-min)Second measurement: 1. hour after starting chemotherapyThe measurement was made immediately after the first hour was full.

Countries

Turkey (Türkiye)

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026