Skip to content

Effect of Laughter Therapy on Surgical Stress, Oxygen Saturation, Pain and Comfort Level

Effect of Laughter Therapy Based on Kolcaba Comfort Theory on Surgical Stress, Oxygen Saturation, Pain and Comfort Level in Bariatric Surgery Patients

Status
Completed
Phases
Phase 4
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05927402
Enrollment
66
Registered
2023-07-03
Start date
2022-07-03
Completion date
2023-12-01
Last updated
2024-01-11

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

Conditions

Bariatric Surgery Pateints, Laughter Yoga, Lauhgter Therapy

Keywords

bariatric surgery patients, laughter therapy, laughter yoga

Brief summary

The aim of this study is to examine the effect of laughter therapy based on Kolcaba comfort theory, on surgical stress, oxygen saturation, pain and comfort level in bariatric surgery patients. The main questions it aims to answer are: 1. Is there a significant difference between salivary cortisol levels of patients with and without laughter yoga before surgical intervention? 2. Is there a significant difference between the blood glucose levels of patients who were and were not treated with laughter yoga before surgical intervention? 3. Is there a significant difference between the mean scores on the perceived stress scale of patients who were and were not treated with laughter yoga before surgical intervention? 4. Is there a significant difference between the oxygen saturation levels of patients with and without laughter yoga before surgical intervention? 5. Is there a significant difference between the mean scores on the comfort level scale of patients who were and were not treated with laughter yoga before surgical intervention? 6. Is there a significant difference between the mean scores on the pain scale of patients who were and were not treated with laughter yoga before surgical intervention? The study population will consist of patients who will apply to the general surgery clinic of Düzce University Research and Application Center between June 2023 and April 2024, who will undergo bariatric surgery and agree to participate in the study. The data collected from these patients will be analyzed. From the patients who meet the inclusion criteria and agree to participate in the study; experimental and control groups will be determined by simple randomization. They will be informed about the research (a 15-minute presentation prepared by the researcher explaining what laughter therapy is) and their verbal and written permission will be obtained. The laughter yoga will be applied to experimanetal group. Every laughter yoga practice is 45 minutes long and is planned 3 times a week for a total of 6 sessions. Control group patients will take only routine nursing care.

Interventions

OTHERLaughter Therapy Based on Kolcaba Comfort Theory

The laughter yoga will be applied to experimanetal group. Every laughter yoga practice is 45 minutes long and is planned 3 times a week for a total of 6 sessions. Control group patients will take only routine nursing care.

Sponsors

Ankara Yildirim Beyazıt University
Lead SponsorOTHER

Study design

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

Eligibility

Sex/Gender
ALL
Age
18 Years to 60 Years
Healthy volunteers
No

Inclusion criteria

* Those who can speak and understand Turkish, * Those who agreed to participate in the study, * Adult age group between 18 and 60 years old, * Those with pain intensity \<2 according to the Visual Comparison Scale, * Those with time and place orientation, * Those without vision and hearing problems, * Those who are literate or have literate relatives, * Those without history of psychiatric illness, * Those without any history of psychotropic drug use and history, * Those without previous laughter yoga practice, * Those with a smartphone/computer/tablet, * Those who undergone laparoscopic sleeve gastrectomy surgery, * Those who can attend the trainings at the specified times so that cortisol is not affected by circadian rhythm, * Those who are able to comply with the collection of saliva samples, * American Society of Anesthesiologist (ASA) score I, II or III as assessed by physicians

Exclusion criteria

* Those who speak Turkish but cannot understand, * Those who are under 18 and over 60 years of age, * Those who are not willing to participate in the study, * Those diagnosed with psychiatric illness, * Those with previous laughter yoga practice, * Those with physical limitations/respiratory problems who cannot perform yoga movements, * Those who have difficulty in doing breathing exercises due to deviated septum etc, * Those who have undergone abdominal surgery in the last six months * Hypothyroidism, hyperaldosteronism, pregnancy, malignancy, congestive heart failure, psychotic disorder, chronic liver failure, uncontrolled hypertension, glaucoma, herniation, nephrotic syndrome, type 2 diabetes mellitus, Patients with a diagnosis of chronic renal failure and continuous use of medication were excluded as salivary cortisol levels may be affected, * Those with an ASA score of 4, * Those who don't undergone laparoscopic sleeve gastrectomy surgery,

Design outcomes

Primary

MeasureTime frameDescription
Stress levelbefore first laughter therapy applicationwith Perceived Stress Scale-14, 0-56 (min-max), higher scores mean worse outcome
Pain levelbefore first laughter therapy applicationwith Visual Analog Scale, 0-10 (min-max), higher scores mean worse outcome
Comfort levelbefore first laughter therapy applicationwith General Comfort Questionaire, 48-192 (min-max), higher scores mean worse outcome
Blood glucose levelbefore first laughter therapy applicationwith blood glucose meter
Oxygen Saturation Levelbefore first laughter therapy applicationwith pulse oximetry
oxygen saturation levelafter sixth laughter therapy application (preop first day)with pulse oximetry
salivary cortisol samplebefore first laughter therapy applicationsalivette cortisol

Countries

Turkey (Türkiye)

Outcome results

None listed

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