Pulmonary Rehabilitation and Quality of Life

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Clinical Phase

NA

Total Enrollment

50 participants

Study Classification

INTERVENTIONAL

Study Start Date

2016-08-01

Study Completion Date

2017-12-29

Brief Summary

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In this study, the effect of a pulmonary rehabilitation (PR) program on the respiratory function and quality of life of patients undergoing CABG surgery with an open-heart technique is examined. A randomized controlled experimental design was used. The study was conducted with two groups: the intervention group (n=25) and control group (n=25). The control group received standard care after CABG. In contrast, the experimental group, in addition to standard care, participated in a PR program created by the researchers. After CABG, the respiratory functions of both groups (clinical care day 4) and quality of life (6th week) evaluated

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Detailed Description

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Conditions

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Coronary Artery Bypass Graft

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Primary Study Purpose

SUPPORTIVE_CARE

Blinding Strategy

DOUBLE

Participants Investigators

Study Groups

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intervention group

standard care and participated in a pulmonary rehabilitation program

Group Type EXPERIMENTAL

pulmonary rehabilitation

Intervention Type OTHER

Simple breathing techniques, secretion-removal techniques, airway-cleaning techniques, mobilization techniques and use of an incentive spirometer

control group

received standard care after coronary artery bypass graft

Group Type NO_INTERVENTION

No interventions assigned to this group

Interventions

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pulmonary rehabilitation

Simple breathing techniques, secretion-removal techniques, airway-cleaning techniques, mobilization techniques and use of an incentive spirometer

Intervention Type OTHER

Eligibility Criteria

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Inclusion Criteria

* Patients who were extubated in twenty-four hours,
* aged 18 or above,
* had undergone CABG surgery using the open-heart method and using a saphenous vein graft for CABG,
* who were conscious,
* without visual and hearing problems,
* who spoke Turkish,
* had not orthopedic, psychiatric and neurological problems,
* no co-morbid lung disease,
* who had not been re-operated on,
* had not postoperative cardiac dysfunction,
* had not developed postoperative atrial fibrillation,
* who were willing to participate in the study.

Exclusion Criteria

* Patients who were not extubated in twenty-four hours,
* who were under 18 years of age,
* had not undergone CABG surgery using the open-heart method and using a saphenous vein graft for CABG,
* who were not conscious,
* were visual and hearing problems,
* who don't spoke Turkish,
* had orthopedic, psychiatric and neurological problems,
* co-morbid lung disease,
* who had been re-operated on,
* had postoperative cardiac dysfunction,
* had developed postoperative atrial fibrillation,
* who were not willing to participate in the study.

Minimum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

Yes