Main
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Note: This record shows only 22 elements of the WHO Trial Registration Data Set. To view changes that have been made to the source record, or for additional information about this trial, click on the URL below to go to the source record in the primary register. |
Register:
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ClinicalTrials.gov |
Last refreshed on:
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19 February 2015 |
Main ID: |
NCT02156284 |
Date of registration:
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03/06/2014 |
Prospective Registration:
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No |
Primary sponsor: |
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Public title:
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Nurse Empathic Behaviour to Reduce the Fear in Patients of Preoperative Cardiac Surgery
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Scientific title:
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Nurse Empathic Behaviour to Reduce the Fear in Patients of Preoperative Cardiac Surgery |
Date of first enrolment:
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May 2011 |
Target sample size:
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44 |
Recruitment status: |
Completed |
URL:
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http://clinicaltrials.gov/show/NCT02156284 |
Study type:
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Interventional |
Study design:
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Intervention Model: Single Group Assignment, Masking: Single Blind (Outcomes Assessor)
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Phase:
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N/A
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Countries of recruitment
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Brazil
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Contacts
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Name:
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Juliana S Jurko |
Address:
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Telephone:
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Email:
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Affiliation:
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Federal University of São Paulo |
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Name:
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Juliana L Lopes, PhD |
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Email:
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Affiliation:
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Federal University of São Paulo |
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Name:
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Alba Lucia B L Barros, PhD |
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Email:
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Affiliation:
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Federal University of São Paulo |
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Name:
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Cinthia C Assis, PhD |
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Telephone:
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Email:
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Affiliation:
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Federal University of São Paulo |
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Key inclusion & exclusion criteria
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Inclusion Criteria:
- Patients older than 18 years
- Patient who agreed to participate in the study by signing the consent form at least
24 hours prior to surgery
Exclusion Criteria:
- Patients in preoperative cardiac transplantation
- Patients who did not have at least two defining characteristics of the nursing
diagnosis fear
- Patients using anxiolytics
- Smokers and / or patients who drank any amount of alcohol daily
Age minimum:
18 Years
Age maximum:
N/A
Gender:
Both
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Health Condition(s) or Problem(s) studied
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Cardiovascular Disease
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Intervention(s)
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Behavioral: Empathic behaviour by nurses
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Primary Outcome(s)
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The primary outcome was Fear.
[Time Frame: Participants were followed for the duration of preoperative period, an expected average of 4 days.]
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Secondary ID(s)
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U111111568736
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Source(s) of Monetary Support
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Please refer to primary and secondary sponsors
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Results
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Results available:
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Date Posted:
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Date Completed:
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URL:
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