CClinicalTrials.gg
CompletedNCT07051616Updated Jul 4, 2025

The Effect of Children's Laughter Video on Oncology Patient

An interventional study of Child laughter video in Anxiety, Chemotherapy Effect and Laughter, sponsored by Selcuk University. Completed at 1 site in Turkey (Türkiye). Open to participants aged 32 Years to 81 Years. Per ClinicalTrials.gov, last updated 2025-07-04.

Sponsored by Selcuk University · Not applicable, Interventional, and Supportive care

From the registry’s dates

  • Registered 1 year 9 months after the study started (first participant enrolled Sep 2023, registered Jun 2025).
Phase
Not applicable
Study type
Interventional
Enrollment
36
Allocation
Randomized
Ages
32 Years to 81 Years
Sex
All
01

Study 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

Read the 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.

02

Conditions studied

  • Anxiety
  • Chemotherapy Effect
  • Laughter
  • Fatigue
  • Nausea
  • Vomiting
03

In context

Anxiety Disorders

4,868 studies on the registry are indexed under Anxiety Disorders; 1,390 are open to participants now.

This study's enrollment of 36 is below the median of 80 across 4,174 interventional studies indexed under Anxiety Disorders.

Browse Anxiety Disorders studies →

Lead sponsor

Selcuk University is the lead sponsor of 248 studies on the registry; 63 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
32 Years to 81 Years
Sexes eligible
All
Accepts 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

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
05

Study design

Phase
Not applicable
Primary purpose
Supportive care
Allocation
Randomized
Intervention model
Parallel assignment
Masking
Single (Participant)
Enrollment
36 participants (actual)

Study arms

  • Experimental
    Child laughter video group

    Patients in this group were made to watch the laughter video prepared by the researchers at the end of the 1st and 2nd hour after the start of chemotherapy.

    Behavioral: Child laughter video

  • No intervention
    Control Group

    Participants in the control group were not subjected to any intervention other than routine practice during chemotherapy.

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.

06

What researchers measure

Primary outcomes

  1. Patient information form

    The form was designed by the researchers in two parts to assess personal characteristics and characteristics related to the disease and treatment.

    Time frame: First measurement-10. minutes before the start of the patient's chemotherapy

  2. Spielberger State Anxiety Scale

    The 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

    Time frame: First measurement- 5 minutes before the start of the patient's chemotherapy

  3. FACIT Fatigue Scale

    Developed 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.

    Time frame: First measurement- 1 minutes before the start of the patient's chemotherapy

  4. Physiological Parameter Follow-up Form (Heart rate-min)

    This form was created by researchers. When chemotherapy started and measured at the beginning of each hour.

    Time frame: As soon as chemotherapy is started (Within first five minute)

  5. Physiological Parameter Follow-up Form (Respiration rate- min)

    This form was created by researchers. When chemotherapy started and measured at the beginning of each hour.

    Time frame: As soon as chemotherapy is started (Within first five minute)

  6. Physiological Parameter Follow-up Form (oxygen saturation -SpO2%)

    This form was created by researchers. When chemotherapy started and measured at the beginning of each hour.

    Time frame: As soon as chemotherapy is started (Within first five minute)

  7. Physiological Parameter Follow-up Form (blood pressure- mmHg)

    This form was created by researchers. When chemotherapy started and measured at the beginning of each hour.

    Time frame: As soon as chemotherapy is started (Within first five minute)

  8. Nausea Follow-up Form

    With this form, the presence or absence of the patient's nause was questioned.Nausea was first measured at the start of chemotherapy

    Time frame: As soon as chemotherapy is started (Within first five minute)

  9. Vomiting Follow-up Form

    With this form, the presence or absence of the patient's vomiting was questioned. Vomiting was first measured at the start of chemotherapy

    Time frame: As soon as chemotherapy is started (Within first five minute)

Secondary outcomes

  1. Physiological Parameter Follow-up Form (Heart rate-min)

    The measurement was made immediately after the first hour was full.

    Time frame: Second measurement: 1. hour after starting chemotherapy

  2. Physiological Parameter Follow-up Form (Respiration rate- min)

    The measurement was made immediately after the first hour was full.

    Time frame: Second measurement: 1. hour after starting chemotherapy

  3. Physiological Parameter Follow-up Form (oxygen saturation -SpO2%)

    The measurement was made immediately after the first hour was full.

    Time frame: Second measurement: 1. hour after starting chemotherapy

  4. Physiological Parameter Follow-up Form (blood pressure- mmHg)

    The measurement was made immediately after the first hour was full.

    Time frame: Second measurement: 1. hour after starting chemotherapy

  5. Nausea Follow-up Form

    The measurement was made immediately after the first hour was full.

    Time frame: Second measurement: 1. hour after starting chemotherapy

  6. Vomiting Follow-up Form

    The measurement was made immediately after the first hour was full.

    Time frame: Second measurement: 1. hour after starting chemotherapy

  7. Physiological Parameter Follow-up Form (Heart rate-min)

    The measurement was made immediately after the second hour was full.

    Time frame: Third measurement: 2. hour after starting chemotherapy

  8. Physiological Parameter Follow-up Form (Respiration rate- min)

    The measurement was made immediately after the second hour was full.

    Time frame: Third measurement: 2. hour after starting chemotherapy

  9. Physiological Parameter Follow-up Form (oxygen saturation -SpO2%)

    The measurement was made immediately after the second hour was full.

    Time frame: Third measurement: 2. hour after starting chemotherapy

  10. Physiological Parameter Follow-up Form (blood pressure- mmHg)

    The measurement was made immediately after the second hour was full.

    Time frame: Third measurement: 2. hour after starting chemotherapy

  11. Nausea Follow-up Form

    The measurement was made immediately after the second hour was full.

    Time frame: Third measurement: 2. hour after starting chemotherapy

  12. Vomiting Follow-up Form

    The measurement was made immediately after the second hour was full.

    Time frame: Third measurement: 2. hour after starting chemotherapy

  13. Physiological Parameter Follow-up Form (Heart rate-min)

    The measurement was made immediately after the third hour was full.

    Time frame: Fourth measurement: 3. hour after starting chemotherapy

  14. Physiological Parameter Follow-up Form (Respiration rate- min)

    The measurement was made immediately after the third hour was full.

    Time frame: Fourth measurement: 3. hour after starting chemotherapy

  15. Physiological Parameter Follow-up Form (oxygen saturation -SpO2%)

    The measurement was made immediately after the third hour was full.

    Time frame: Fourth measurement: 3. hour after starting chemotherapy

  16. Physiological Parameter Follow-up Form (blood pressure- mmHg)

    The measurement was made immediately after the third hour was full.

    Time frame: Fourth measurement: 3. hour after starting chemotherapy

  17. Nausea Follow-up Form

    The measurement was made immediately after the third hour was full.

    Time frame: Fourth measurement: 3. hour after starting chemotherapy

  18. Vomiting Follow-up Form

    The measurement was made immediately after the third hour was full.

    Time frame: Fourth measurement: 3. hour after starting chemotherapy

  19. Physiological Parameter Follow-up Form (Heart rate-min)

    The measurement was made immediately after the fourth hour was full.

    Time frame: Fifth measurement: 4. hour after starting chemotherapy

  20. Physiological Parameter Follow-up Form (Respiration rate- min)

    The measurement was made immediately after the fourth hour was full.

    Time frame: Fifth measurement: 4. hour after starting chemotherapy

  21. Physiological Parameter Follow-up Form (oxygen saturation -SpO2%)

    The measurement was made immediately after the fourth hour was full.

    Time frame: Fifth measurement: 4. hour after starting chemotherapy

  22. Physiological Parameter Follow-up Form (blood pressure- mmHg)

    The measurement was made immediately after the fourth hour was full.

    Time frame: Fifth measurement: 4. hour after starting chemotherapy

  23. Nausea Follow-up Form

    The measurement was made immediately after the fourth hour was full.

    Time frame: Fifth measurement: 4. hour after starting chemotherapy

  24. Vomiting Follow-up Form

    The measurement was made immediately after the fourth hour was full.

    Time frame: Fifth measurement: 4. hour after starting chemotherapy

07

Study locations

1 site
  • Sibel Küçükoğlu
    Selçuklu, Akademi Mahallesi, Turkey (Türkiye)
08

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Jul 4, 2025, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
09

Registry details

Key details

Study ID
NCT07051616
Lead sponsor
Selcuk University
Responsible party
Sibel Küçükoğlu (Prof, Selcuk University) — Principal investigator
First posted
Jul 4, 2025
Start date
Sep 15, 2023
Primary completion
May 30, 2025
Completion
May 30, 2025
Last update
Jul 4, 2025

Study contacts

Sibel Kucukoglu, Prof
principal investigator · Selcuk University

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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