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The Effect of Breathing Exercise Applied With Incentive Spirometer

T

TC Erciyes University

Status

Completed

Conditions

Incentive Spirometry
Cardiac Surgery
Breathing Exercises

Treatments

Other: The post-surgical breathing exercise group
Other: The pre- and post- surgical breathing exercise group

Study type

Interventional

Funder types

Other

Identifiers

Details and patient eligibility

About

It was conducted as a single-center, prospective, randomized controlled experimental study. Data were collected with the Introductory Information Form, Numerical Rating Scale, Physiological Parameters Follow-up Form and General Comfort Scale.

Full description

It was conducted as a single-center, prospective, randomized controlled experimental study. Data were collected with the Introductory Information Form, Numerical Rating Scale, Physiological Parameters Follow-up Form and General Comfort Scale.The study was conducted in three groups. Individuals in the intervention-1 group were asked to perform breathing exercises with IS in addition to the routine practices of the clinic for 5 days in the postoperative period. Individuals in the intervention-1 group were asked to perform breathing exercises with IS in addition to the routine practices of the clinic for a total of 10 days, 5 days in the preoperative period and 5 days in the postoperative period. Individuals in the control group were given only the routine practice of the clinic.

Enrollment

75 patients

Sex

All

Ages

18 to 75 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Able to communicate in Turkish,
  • undergoing cardiac surgery,
  • no pain in the preoperative period (0 pain according to VA),
  • have no problems with vision, hearing or speech,
  • individuals who agreed to participate in the study were included.

Exclusion criteria

  • Using psychiatric medication,
  • Using immunosuppressive medication until 30 days before surgery,
  • with neuromuscular disorders,
  • having rheumatic disease,
  • have had pulmonary surgery before,
  • with cerebrovascular injury,
  • diagnosed with cardiovascular instability or aneurysm,
  • Diagnosed with COPD,
  • individuals who do not volunteer to participate in the study

Trial design

Primary purpose

Supportive Care

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

75 participants in 3 patient groups

The post-surgical breathing exercise group
Experimental group
Description:
Individuals in this group were asked to perform 10 breathing exercises with IS every waking hour in addition to the routine practices of the clinic for 5 days in the postoperative period.
Treatment:
Other: The post-surgical breathing exercise group
The pre- and post- surgical breathing exercise group
Experimental group
Description:
Individuals in this group were asked to perform 10 breathing exercises with IS every waking hour in addition to the routine practices of the clinic for a total of 10 days, 5 days in the preoperative period and 5 days in the postoperative period.
Treatment:
Other: The pre- and post- surgical breathing exercise group
Control group
No Intervention group
Description:
Routine practice group

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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