Actively Recruiting

Phase Not Applicable
Age: 18Years +
All Genders
Healthy Volunteers
ID06415890

Effect of Using the 4-7-8 Breathing Technique on Postoperative Shoulder Pain and Respiratory Function After Laparoscopic Cholecystectomy

Led by Mustafa Kemal University · Updated on 2024-09-19

98

Participants Needed

1

Research Sites

13 weeks

Total Duration

On this page

Sponsors

M

Mustafa Kemal University

Lead Sponsor

M

Mersin University

Collaborating Sponsor

AI-Summary

What this Trial Is About

Researchers are evaluating the effect of the 4-7-8 breathing technique on shoulder pain and lung function after laparoscopic cholecystectomy, a common surgery for gallbladder removal. This technique is being studied because many patients experience shoulder pain and reduced lung function after surgery, which can affect breathing and recovery. The study will randomly assign 96 patients to either the breathing exercise group or a control group receiving routine care, to compare outcomes. The study group will learn the 4-7-8 breathing technique, which involves controlled breathing cycles, starting about four hours after surgery. They will practice one set of four breaths every two hours, with initial training lasting about 15 minutes. The control group will receive usual care without specific breathing exercise training, though use of a breathing aid is recommended but not monitored. Participants will be monitored for shoulder pain and lung function through tests conducted within the first 24 hours and again at discharge. The study will assess lung volumes and airflow measures to understand breathing recovery. Data will be analyzed statistically. The total duration of participation varies with hospital stay but includes monitoring through the early postoperative period for safety and effectiveness.

CONDITIONS

Brief Title

Effect of 4-7-8 Breathıng Technıque on Shoulder Paın and Respıratory Functıon Tests After Laparoscopıc Cholesectectomy

Who Can Participate

Age: 18Years +
All Genders
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • Undergoing elective laparoscopic cholecystectomy
  • Admitted to the clinic at least 2 hours before surgery
  • Able to communicate and cooperate
  • Provided written and verbal consent to participate
  • Conscious, oriented, and cooperative
  • No cognitive or mental problems
  • Speaks and understands Turkish
  • American Society of Anesthesiologists (ASA) score I or II
  • Hospitalized at least one night after surgery
  • Age 18 years or older
Not Eligible

You will not qualify if you...

  • Undergoing emergency laparoscopic cholecystectomy
  • Undergoing open cholecystectomy
  • Not admitted to the clinic at least 2 hours before surgery
  • Unable to communicate or cooperate
  • Did not provide written and verbal consent
  • Unconscious, disoriented, or uncooperative
  • Cognitive or mental impairment
  • Speaks Turkish but does not understand it
  • Discharged on the same day after surgery
  • ASA score III or higher
  • Age 18 years or younger

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

1 visit (in-person) before surgery

Surgery

Duration - Less than 24 hours

Participants undergo laparoscopic cholecystectomy as part of their routine clinical care.

Hospital stay of at least one night after surgery

Treatment

Duration - From 4 hours after surgery until discharge (typically within 24 hours post-surgery)

Participants in the breathing exercise group learn and perform the 4-7-8 breathing technique starting 4 hours after surgery, performing one set every two hours. Participants in the control group receive routine care without specific breathing exercise training.

Multiple visits for breathing exercise sessions every 2 hours starting 4 hours after surgery until discharge

Post-operative Follow-up

Duration - Up to 2 days post-surgery

Participants' shoulder pain and pulmonary function are monitored on the second postoperative day to assess recovery and effects of the intervention.

1 visit on the second postoperative day

Trial Site Locations

Total: 1 location

1

İskenderun Devlet Hastanesi

Hatay, Turkey (Türkiye), 31000

Actively Recruiting

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Research Team

A

Ayşe Nur SERBEST BAZ

G

Gülay ALTUN UĞRAŞ

How is the study designed?

Study Type

INTERVENTIONAL

Masking

DOUBLE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

SUPPORTIVE_CARE

Number of Arms

2

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Published Research Related To This Trial

Investigating the effects of drainage by hemovac drain on shoulder pain after female laparoscopic surgery and comparison with deep breathing technique: a randomized clinical trial study.

Fatemeh Hosseinzadeh, Ebrahim Nasiri, Tahereh Behroozi

https://pubmed.ncbi.nlm.nih.gov/31932939

The Effect of Deep Breathing Exercise and 4-7-8 Breathing Techniques Applied to Patients After Bariatric Surgery on Anxiety and Quality of Life.

Gülfidan Kurt Aktaş, Vesile Eskici İlgin

https://pubmed.ncbi.nlm.nih.gov/36480101

Effects of sleep deprivation and 4-7-8 breathing control on heart rate variability, blood pressure, blood glucose, and endothelial function in healthy young adults.

Jaruwan Vierra, Orachorn Boonla, Piyapong Prasertsri

https://pubmed.ncbi.nlm.nih.gov/35822447

The Effects of Aroma Essential Oil Inhalation on Stress, Pain, and Sleep Quality in Laparoscopic Cholecystectomy Patients: A Randomized Controlled Trial.

JiA Lee, Myung-Haeng Hur

https://pubmed.ncbi.nlm.nih.gov/34954406