跳至主要内容
临床试验/NCT05927402
NCT05927402已完成4 期

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

Ankara Yildirim Beyazıt University2 个研究点 分布在 2 个国家目标入组 66 人开始时间: 2022年7月3日最近更新:
适应症

试验速览

阶段
4 期
状态
已完成
发起方
入组人数
66
试验地点
2
主要终点
Comfort level

研究概览

简要总结

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.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Supportive Care
盲法
Single (Participant)

入排标准

年龄范围
18 Years 至 60 Years(Adult)
性别
All
接受健康志愿者

入选标准

  • 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

排除标准

  • 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,

结局指标

主要结局

Comfort level

时间窗: postop first day

with General Comfort Questionaire, 48-192 (min-max), higher scores mean worse outcome

Stress level

时间窗: postop first day

with Perceived Stress Scale-14, 0-56 (min-max), higher scores mean worse outcome

Oxygen Saturation Level

时间窗: postop first day

with pulse oximetry

oxygen saturation level

时间窗: after sixth laughter therapy application (preop first day)

with pulse oximetry

salivary cortisol sample

时间窗: postop first day

salivette cortisol

Pain level

时间窗: postop first day

with Visual Analog Scale, 0-10 (min-max), higher scores mean worse outcome

Blood glucose level

时间窗: postop first day

with blood glucose meter

次要结局

未报告次要终点

研究者

发起方
Ankara Yildirim Beyazıt University
申办方类型
Other
责任方
Principal Investigator
主要研究者

Gülşah Kayserilioğlu

Lecturer

Ankara Yildirim Beyazıt University

研究点 (2)

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