Self-Efficacy Levels of Nurses on Safe Blood and Blood Product Transfusion

NCT06542185 | Completed

• 1 other identifier: ABAHAR-003
• Study Type: interventional
• Target: 90
• Locations: 1 country
• Sites: 1

Brief Summary

A quasi-experimental study was conducted in a pre-test-post-test design to investigate the self-efficacy levels of nurses working in a cardiovascular surgery Intensive Care Unit regarding safe blood and blood product transfusion and the effects of online training.

Conditions

To Evaluate the Effect of Online Education on Nurses' Self-efficacy Regarding Blood Transfusion

Keywords

nurse; blood transfusion; To evaluate the effect of online education on nurses' self-efficacy regarding blood transfusion practices.

Outcome Measures

Primary Outcomes (1)

• Personal Information Form

  This form, prepared by researchers, includes a total of 13 questions that include nurses' personal and professional characteristics as well as their experiences with blood transfusion (age, gender, professional experience, education, having performed a transfusion, etc.).

  20 minutes

Secondary Outcomes (1)

• Blood Products Transfusion Self-Efficacy Scale (SBT-SES)

  50 minutes

Study Arms (2)

online education

EXPERIMENTAL

\- Nurses' self-efficacy levels regarding safe blood transfusion practices will be measured with the Safe Blood and Blood Products Transfusion Self-Efficacy Scale (SBT-SES). SBT-SES pre-tests will be applied to the control and intervention groups, and online training on safe blood transfusion prepared by the researcher will be provided to the intervention group. After the training given to the intervention group, SBT-SES post-tests will be applied to both the intervention and control groups.

Other: online education

control

NO INTERVENTION

No training will be given, only the Blood Products Transfusion Self-Efficacy Scale (SBT-SES) pre-test and post-test will be conducted.

Interventions

online education OTHER

online education

online education

Eligibility Criteria

• Age: 28 Years - 65 Years
• Sex: all
• Healthy Volunteers: Yes
• Age Groups: Adult (18-64), Older Adult (65+)

You may qualify if:

• volunteer nurses

You may not qualify if:

• Nurses who did not want to participate in the study

Sponsors & Collaborators

• Yuksek Ihtisas University: lead

Study Sites (1)

Yüksek Ihtisas University

Ankara, Çankaya, Turkey (Türkiye)

Location

Study Officials

• arzu bahar

  Yüksek Ihtisas University

  PRINCIPAL INVESTIGATOR

Study Design

• Study Type: interventional
• Phase: not applicable
• Allocation: RANDOMIZED
• Masking: SINGLE
• Who Masked: PARTICIPANT
• Purpose: OTHER
• Intervention Model: PARALLEL
• Sponsor Type: OTHER
• Responsible Party: PRINCIPAL INVESTIGATOR
• PI Title: Yüksek Ihtisas University

Model Details: Parallel Assignment a clinical trial with experimental and control groups

Study Record Dates

• First Submitted: August 2, 2024
• First Posted: August 7, 2024
• Study Start: May 20, 2024
• Primary Completion: July 20, 2024
• Study Completion: July 30, 2024
• Last Updated: August 7, 2024

Record last verified: 2024-08

Data Sharing

• IPD Sharing: Will not share

Locations

TU (1)