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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: ClinicalTrials.gov
Last refreshed on: 19 February 2015
Main ID:  NCT02156284
Date of registration: 03/06/2014
Prospective Registration: No
Primary sponsor: Federal University of São Paulo
Public title: Nurse Empathic Behaviour to Reduce the Fear in Patients of Preoperative Cardiac Surgery
Scientific title: Nurse Empathic Behaviour to Reduce the Fear in Patients of Preoperative Cardiac Surgery
Date of first enrolment: May 2011
Target sample size: 44
Recruitment status: Completed
URL:  http://clinicaltrials.gov/show/NCT02156284
Study type:  Interventional
Study design:  Intervention Model: Single Group Assignment, Masking: Single Blind (Outcomes Assessor)  
Phase:  N/A
Countries of recruitment
Brazil
Contacts
Name:     Juliana S Jurko
Address: 
Telephone:
Email:
Affiliation:  Federal University of São Paulo
Name:     Juliana L Lopes, PhD
Address: 
Telephone:
Email:
Affiliation:  Federal University of São Paulo
Name:     Alba Lucia B L Barros, PhD
Address: 
Telephone:
Email:
Affiliation:  Federal University of São Paulo
Name:     Cinthia C Assis, PhD
Address: 
Telephone:
Email:
Affiliation:  Federal University of São Paulo
Key inclusion & exclusion criteria

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
Health Condition(s) or Problem(s) studied
Cardiovascular Disease
Intervention(s)
Behavioral: Empathic behaviour by nurses
Primary Outcome(s)
The primary outcome was Fear. [Time Frame: Participants were followed for the duration of preoperative period, an expected average of 4 days.]
Secondary Outcome(s)
Secondary ID(s)
U111111568736
Source(s) of Monetary Support
Please refer to primary and secondary sponsors
Secondary Sponsor(s)
Ethics review
Results
Results available:
Date Posted:
Date Completed:
URL:
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