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Preoperatively Orientation in Cardiac Surgery: Nurses Intervention on Patients Recovery

Primary Purpose

Coronary Artery Bypass Graft Triple Vessel, Heart Valve Diseases

Status
Completed
Phase
Not Applicable
Locations
Brazil
Study Type
Interventional
Intervention
Intervention Group
Sponsored by
Instituto de Cardiologia do Rio Grande do Sul
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional supportive care trial for Coronary Artery Bypass Graft Triple Vessel focused on measuring cardiac surgery, orientation, nursing

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Primary Elective Cardiac Surgical Procedures
  • Age above 18 years old
  • At least 24 hours of hospitalization before the procedure

Exclusion Criteria:

  • Patients who do not accept and do not signed a consenting term

Sites / Locations

  • Institute of Cardiology

Arms of the Study

Arm 1

Arm 2

Arm Type

No Intervention

Other

Arm Label

Control Group

Group intervention

Arm Description

Received preoperative guidance by a member of healthcare team with the aid of checklist

preoperative guideline by a nurse

Outcomes

Primary Outcome Measures

knowledge
three questions applied on the second day of recovery at the nursery room, after the intensive care unit discharge,about type of anesthesia,endotracheal tube function and time of healing of the sternum bone.The questions had only one correct alternative.Since the randomization until the questionnaire,the study follow up took seven days.For the analysis,answers of the questionnaire were separated and the number of answers for each,and divided into the two groups.The results were presented in graphic and tables.

Secondary Outcome Measures

satisfaction
five questions applied on the second day of recovery at the nursery room.The patients had to graduate their level of satisfaction from unsatisfied to very satisfied according to orientation received about the prior,intraoperative and recovering period of surgery as well as the nursery and medical orientation provided.Since the randomization until the questionnaire,the study follow up took seven days.For the analysis answers of the questionnaire were separated and the number of answers for each,and divided into the two groups.The results were presented in graphic and tables.

Full Information

First Posted
February 23, 2012
Last Updated
March 19, 2012
Sponsor
Instituto de Cardiologia do Rio Grande do Sul
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1. Study Identification

Unique Protocol Identification Number
NCT01559610
Brief Title
Preoperatively Orientation in Cardiac Surgery: Nurses Intervention on Patients Recovery
Official Title
Preoperatively Orientation in Cardiac Surgery: Nurses Intervention on Patients Recovery
Study Type
Interventional

2. Study Status

Record Verification Date
March 2012
Overall Recruitment Status
Completed
Study Start Date
August 2008 (undefined)
Primary Completion Date
March 2009 (Actual)
Study Completion Date
March 2009 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Instituto de Cardiologia do Rio Grande do Sul

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
The purpose of this study is to determine whether the guidelines preoperative performed by a nurse contribute to the recovery of the patient submitted to cardiac surgery compared with the guidelines for routine.
Detailed Description
This is a randomized clinical trial, which included patients submitted to cardiac surgery on both sexes. They are divided in two groups: control group and intervention group.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Coronary Artery Bypass Graft Triple Vessel, Heart Valve Diseases
Keywords
cardiac surgery, orientation, nursing

7. Study Design

Primary Purpose
Supportive Care
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
Participant
Allocation
Randomized
Enrollment
180 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Control Group
Arm Type
No Intervention
Arm Description
Received preoperative guidance by a member of healthcare team with the aid of checklist
Arm Title
Group intervention
Arm Type
Other
Arm Description
preoperative guideline by a nurse
Intervention Type
Other
Intervention Name(s)
Intervention Group
Other Intervention Name(s)
No applicable
Intervention Description
The patients were instructed by a nurse
Primary Outcome Measure Information:
Title
knowledge
Description
three questions applied on the second day of recovery at the nursery room, after the intensive care unit discharge,about type of anesthesia,endotracheal tube function and time of healing of the sternum bone.The questions had only one correct alternative.Since the randomization until the questionnaire,the study follow up took seven days.For the analysis,answers of the questionnaire were separated and the number of answers for each,and divided into the two groups.The results were presented in graphic and tables.
Time Frame
seven days
Secondary Outcome Measure Information:
Title
satisfaction
Description
five questions applied on the second day of recovery at the nursery room.The patients had to graduate their level of satisfaction from unsatisfied to very satisfied according to orientation received about the prior,intraoperative and recovering period of surgery as well as the nursery and medical orientation provided.Since the randomization until the questionnaire,the study follow up took seven days.For the analysis answers of the questionnaire were separated and the number of answers for each,and divided into the two groups.The results were presented in graphic and tables.
Time Frame
seven days

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Primary Elective Cardiac Surgical Procedures Age above 18 years old At least 24 hours of hospitalization before the procedure Exclusion Criteria: Patients who do not accept and do not signed a consenting term
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Juliane A Rodrigues, nursing
Organizational Affiliation
Brasil:Instituto de Cardiologia do Rio Grande do Sul/Fundacao Universitaria de Cardiologia
Official's Role
Principal Investigator
Facility Information:
Facility Name
Institute of Cardiology
City
Porto Alegre
State/Province
Rio Grande do Sul
ZIP/Postal Code
90620001
Country
Brazil

12. IPD Sharing Statement

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Preoperatively Orientation in Cardiac Surgery: Nurses Intervention on Patients Recovery

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