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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT05462665
Other study ID # tPA Treatment
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date May 1, 2020
Est. completion date March 1, 2022

Study information

Verified date December 2021
Source Dokuz Eylul University
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Intravenous (IV) tissue plasminogen activator (tPA) is one of the key elements of acute ischemic stroke. In this study, acute stroke patients maximum benefit from the treatment, intravenous tissue plasminogen activator (IV tPA) minimizing the errors related to the treatment of acute ischemic stroke patients of nursing students from clinical practice guides published on the treatment of It is aimed to be informed and to standardize nursing interventions.


Description:

Time management in acute stroke patients is possible with a multidisciplinary approach and team members who have received specific training for acute stroke patients. Studies have shown that the maximum result of treatment for acute stroke patients depends on nurses' ability to identify disease symptoms, plan and apply symptom-specific nursing care. There is evidence that the multidisciplinary presence of stroke teams in stroke units and the delivery of coordinated care during the acute phase improve patient outcomes . Coordinated care by the stroke team improves patient outcomes, reduces hospital costs, reduces patient readmission, and improves patient care quality.


Recruitment information / eligibility

Status Completed
Enrollment 75
Est. completion date March 1, 2022
Est. primary completion date March 1, 2022
Accepts healthy volunteers No
Gender All
Age group 18 Years to 30 Years
Eligibility Inclusion Criteria: Intern nursing student at Dokuz Eylül University Exclusion Criteria: Those who did not agree to participate in the study Those who were not be intern

Study Design


Related Conditions & MeSH terms


Intervention

Behavioral:
theory training
theory training
theory and simulation training
theory and simulation training

Locations

Country Name City State
Turkey Ozge Soydaner Izmir

Sponsors (1)

Lead Sponsor Collaborator
Dokuz Eylul University

Country where clinical trial is conducted

Turkey, 

Outcome

Type Measure Description Time frame Safety issue
Primary self-efficacy scale Effectiveness change of Intravenous tissue plasminogen activator treatment knowledge after theoric teaching Change from baseline in Intravenous Tissue Plasminogen Activator Treatment knowledge and 2 weeks after intervention
Primary simulation scale evaluation the simulation design 2 weeks after simulation training
Primary tPA treatment information form Effectiveness change of Intravenous tissue plasminogen activator treatment knowledge after simulation and theoric teaching Change from baseline in Intravenous Tissue Plasminogen Activator Treatment knowledge and 2 weeks after intervention
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