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Clinical Trials/NCT06521346
NCT06521346
Completed
Not Applicable

The Effect of Active Cycle Breathing Technique on Respiratory Parameters, Dyspnea Related Kinesiophobia and Pain in Early Post Cardiac Surgery Patients

Damanhour University1 site in 1 country120 target enrollmentDecember 1, 2024

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Respiratory Complication
Sponsor
Damanhour University
Enrollment
120
Locations
1
Primary Endpoint
Respiratory parameters
Status
Completed
Last Updated
4 months ago

Overview

Brief Summary

This study aims to improve pulmonary function impairment is associated with a reduction in chest expansion, lung volume, pain perception and an impairment of the Post cardiac surgery patient's ability to cough effectively. The technique of active cycle breathing consisted of three parts to the ACBT, which are:

  • breathing control
  • deep breaths
  • huff or cough

Detailed Description

This study aims to explore the effect of Active Cycle Breathing Technique on Respiratory Parameters and Pain in Early Post Cardiac Surgery Patients Research hypothesis: -Post cardiac surgery patients who practice active breathing techniques exhibit an improvement in clinical outcomes compared to those who do not practice. Research design: A randomized control trial research design will be utilized to conduct this study. Study Setting: This study was carried out at the cardiac ICUs. A sample of 120 cardiac patients will be assigned in the current study from the previously mentioned settings. The patients will be allocated into two equal groups, each with 60 patients. The control group will be composed of 60 patients who were managed by routine cardiac care The study group will consist of 60 patients who were exposed to an active cycle of breathing techniques Inclusion criteria: * Adult patients of both genders. * After extubating for at least 6 hours * Hemodynamic stable patients * Able to communicate. Exclusion criteria: Patient with complication postoperative surgery Patient's demographic characteristics as patient's code, age, gender, marital status, education, and occupation. Study group: managed by the use of active cycle breathing techniques combined with routine physiotherapy. * Each session of the active cycle breathing technique lasted for 10 to 20 minutes. * The active cycle breathing technique was carried out for three days post extubating four sessions done daily. Implementation of active cycle breathing technique * Explain the steps of ACBT to the patient. * The patient was placed in a semi-sitting position with her or his back straight, and instructions were given to the patient to do the following steps: 1 . Breathing control phase * Hold the spirometer straight. * Exhale, then seal your lips around the mouthpiece and inhale slowly and deeply into your mouth. * The piston in the incentive spirometer's transparent chamber will rise when you inhale deeply. * Hold your breath for 3 to 5 seconds after taking a deep breath. * Remove the mouthpiece and slowly exhale. For a few seconds, until the piston descends to the bottom of the chamber, relax and breathe normally. * To regain control of their breathing, the patient was told to do lengthy, slow expirations between 5 and 7 times. 2 . Thoracic expansion exercises The patient was instructed to relax your upper chest. * The patient was instructed to breathe slowly and deeply through the nose without using the accessory muscle. * The patient was instructed to hold their breath initially for 3 to 4 seconds and gradually increase it to the maximum time. Don't force the breath out; instead, softly exhale through pursed lips until your lungs are empty. * Repeat the previous steps from 3to4 times. 3- Forced expiration technique (huffing) * Patient was instructed to support the incision site by using a chest binder or keeping your hands over your incision. * Cough twice as many times as they huffed two to three times. * This step was repeated a minimum of two times and a maximum of three times in one session.

Registry
clinicaltrials.gov
Start Date
December 1, 2024
End Date
October 31, 2025
Last Updated
4 months ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • Adult patients of both genders.
  • After extubating for at least 6 hours post operation.
  • Hemodynamic stable patients
  • Able to communicate.

Exclusion Criteria

  • Instability of patient's medical condition or hemodynamic instability

Outcomes

Primary Outcomes

Respiratory parameters

Time Frame: Three observation days

change in respiratory rate

Pain perception

Time Frame: Three observation days

Using visual analogue scale score 0 mean no pain while score 10 means sever pain

Dyspnea-related kinesiophobia

Time Frame: preoperative, three observation days, and day of discharge

comprises 11 items include five items dyspnea and six items for fear of activity dimension and each item is rated from "strongly disagree" (score = 1) to "strongly agree" (score = 5) for a total score between 11 and 55.

Secondary Outcomes

  • Deterioration in clinical parameters such as vital signs(Three observation days)
  • ICU and hospital stay(three observation days)

Study Sites (1)

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