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The Effect of Care Bundle in Heart Surgery

H

Harran University

Status

Completed

Conditions

Patient Care Bundles
Thoracic Surgery

Treatments

Procedure: Care Bundle Implementation

Study type

Interventional

Funder types

Other

Identifiers

NCT05667467
Harran University

Details and patient eligibility

About

This study is a quasi-experimental (non-randomized) design study with control and study group patients undergoing open heart surgery. The main purpose of the research to examine the effect of the care bundle application on the quality of recovery and respiratory patterns (respiratory rate, presence of dyspnea, oxygen saturation, etc.) in patients with open heart surgery. The other purpose is examine the compliance rates of nurses in the implementation of the cardiac surgery care bundle on patients. In the study, nurses working in the cardiovascular surgery clinic and surgical intensive care unit in a training and research hospital in southeast Turkey voluntarily applied the care bundle created by the researcher to the patients in the study group. When the data of the study were examined, it was seen that the respiratory patterns and recovery status of the patients who received the care bundle were better. However, it was determined that the compliance rate of the nurses to the care bundle was not at the desired level.

Full description

Introduction: There are several ways to transfer evidence-based practice to the clinic. One of them is "care bundle" implementation.

Purpose: To examine the effect of applying the "Cardiac Surgery Care Bundle" which consists of evidence-based applications, on patients with open heart surgery (AKC) on the quality of recovery and respiratory patterns (respiratory rate, presence of dyspnea, oxygen saturation, etc.). In the study, the compliance status of nurses in the implementation of the care bundle was also examined.

Method:This research is a quasi-experimental, non-randomized study with AKC applied control and study groups. In the study, volunteer nurses working in the surgical intensive care and cardiovascular surgery clinics applied the care bundle created by the researcher to the patients in the study group. care bundle; It includes "Informing the Patients and Their Relatives", "Respiratory Management" and "Early Mobilization" implementations. A total of 103 patients, 69 of whom were control and 34 were study, were included in the study. First, the data of the control group and then the study group were collected. Patients in the control group received standard care, while the study group received a care bundle in addition to the standard care. Data were obtained using the "Descriptive Characteristics Data Form", "Patient Outcomes for Complications Form" and the "Quality of Recovery-40-QoR-40".

Statistical analyses were performed using the IBM SPSS for Windows 22.0 software. The variables were analyzed for normality of distribution using skewness and kurtosis coefficients. Normally distributed variables were presented using mean ± standard deviation values and non-normally distributed variables were presented using median (minimum-maximum) values. Differences between two samples were analyzed using the "Independent Samples t test" when the assumption of normality was met, and using the "Mann-Whitney U" test when the assumption of normality was not met. Categorical variables were analyzed using Chi-square or Fisher's exact tests. Statistical significance was set at p < 0.05.

Enrollment

103 patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Inclusion Criteria for Patients

    • 18 years and older,
    • Elective AKC planned
    • Those who will undergo cardiac surgery for the first time
    • Extubated after cardiac surgery and not given sedating drugs
    • No communication barrier (including hearing and vision problems),
    • Does not have a musculoskeletal disease or neurological problem that will prevent walking after surgery,
    • Does not have any respiratory disease,
    • Psychiatric, not diagnosed with mental illness,
    • Those who volunteered to participate in the research
    • Patients who are 18 years of age or older who volunteer to participate in the research.
  • Inclusion Criteria for Nurses

    • Working as a nurse in cardiovascular surgery clinic or surgical intensive care clinic,
    • It is the nurses who volunteer to participate in the research.

Exclusion criteria

  • Exclusion Criteria for Patients

    • Patients with active bleeding after surgery
    • Developing neurological complications
    • Complications that prevent the patient from standing up after surgery
    • Those with respiratory problems that will delay weaning from the mechanical ventilator
    • Re-operated due to the development of any complication
    • Those who want to leave the research during the pre- or post-surgical research process
    • These are the patients who develop a situation where they cannot continue to accompany the patient while they are accompanying the patient, or who are the relatives of the patients who want to leave the research during the research process.
  • Exclusion Criteria for Nurses

    • Assigned to another clinic during the research process,
    • Resigned from his job during the research process,
    • Nurses who want to leave the study during any phase of the study.

Trial design

Primary purpose

Supportive Care

Allocation

Non-Randomized

Interventional model

Factorial Assignment

Masking

None (Open label)

103 participants in 3 patient groups

CONTROL GROUP
Experimental group
Treatment:
Procedure: Care Bundle Implementation
NURSE GROUP
Experimental group
Treatment:
Procedure: Care Bundle Implementation
STUDY GROUP
Experimental group
Treatment:
Procedure: Care Bundle Implementation

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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