Incentive Spirometry Versus Inspiratory Muscle Training After Coronary Artery Bypass Grafting

Trial statusNot yet recruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexMale
Age50-60
SponsorCairo University

About this trial

This study will be conducted to compare between incentive spirometry verses inspiratory muscle training preoperatively on (ABG) after coronary artery bypass graft surgery.

Is there any significant difference of preoperative incentive spirometry verses inspiratory muscle training on Arterial blood gases (ABG) after coronary artery bypass graft surgery?

Participants will:

Group A (incentive spirometry group ) Group B (Inspiratory muscle trainer group ) for 5 days before operative Group C (control group) and group a , b will have routinely postoperative

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

45 male patients will be included in this study.

Patients with age from 50 to 60 years old (undergoing coronary artery bypass graft surgery) through median sternotomy.

Their body mass index from 25 to 29.9 kg/m2

Patients will be alert and able to follow instruction.

Disqualifiers

Who are expected not to be able to conduct or comply with IS and IMT.

Patients with cognitive or neurological deficits.

Patients with coexisting acute or chronic respiratory disorders.

Patients unable to understand or show the proper use of the incentive spirometer and Inspiratory muscle training .

Trial design

Design model

Parallel

Treatments tested in this trial

  • Incentive spirometry

    Device

    This group will include 15 patients, Incentive spirometry was utilized by the patient with ten breaths, six sets per day for a period of 10 min within patient tolerance in every session for five days with routinely physical therapy program (education and explanation) preoperatively, And postoperatively treatment (breathing treatment, deep-breathing applications, guided coughing, early mobilization).

  • Inspiratory muscle trainer

    Device

    This group will include 15 patients, each session consisted of 30 minutes of inspiratory muscle training. The patients were trained to use an inspiratory threshold-loading device (Threshold Inspiratory Muscle Training) for five days with routinely physical therapy program (education and explanation) preoperatively, And postoperatively treatment (breathing treatment, deep-breathing applications, guided coughing, early mobilization).

  • Routine physical therapy

    Other intervention

    15 patients will receive for 5 days routinely physical therapy program (education and explanation) preoperatively, And postoperatively treatment (breathing treatment, deep-breathing applications, guided coughing, early mobilization).

Treatment groups

45 Participants
are divided into 3 treatment groups
Group A: ISExperimental treatment 1 intervention
Group B: IMTExperimental treatment 1 intervention
Group C: Control groupActive comparator 1 intervention

Trial outcomes

Primary outcomes

1

Arterial Blood gas Parameters (PaO2 and SaO2)

Assessment of arterial oxygenation changes by measuring PaO2 and SaO2 . data will be collected at Baseline pre-surgery (5 days ) , Immediately after the surgery (within 48 hours) , and through study completion an average of 8 days.to evaluate the recovery trend and the effectiveness of respiratory interventions.

Time frame
Baseline 5 days pre-surgery , Immediately after the surgery within 48 hours , and through study completion an average of 8 days.

Secondary outcomes

1

Atelactasis

Assessment of lung collapse using chest X-ray and CT or clinical findings.

Time frame
Baseline 5 days pre-surgery, Immediately after the surgery within 48 hours, and through study completion an average of 8 days.
2

Functional capacity (2- minute walk test)

measuring the maximum distance a patient can walk on a flat surface in 2-minutes to evaluate functional exercise capacity.

Time frame
Baseline 5 days pre-surgery, and through study completion an average of 8 days.
3

Physical function ICU test - scored (PFIT-s)

Assessment of physical function in the ICU through four components ( sit -to- stand, marching, shoulder flexion, and knee extension ) Scored (0 - 10).

Time frame
Immediately after the surgery within 48 hours.
4

Mechanical Ventilation duration

the total number of hours the patient required mechanical ventilation support after CABG surgery

Time frame
from the end of surgery until successful extubation .

Other outcomes

Sponsors and contacts

Click on the lead sponsor to view all of their trials.

This trial is not recruiting at the moment. You can still explore other options: