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Completed

NCT Number: NCT05625672

EFFICIENCY OF HEMOVIGILANCE MODULE TRAININGS GIVEN TO NURSES

The aim of the present study is to determine the effectiveness of hemovigilance module training given to nurses.

Completed

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Key information

Age range

18 year–64 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Ankara Yıldırım Beyazıt University

Ankara, Turkey (Türkiye)

About this study

125 nurses from the clinic and intensive care units, who received the most intensive blood transfusion from two different hospitals, were included in the study as the intervention and control groups. The control group was not trained. Only the pretest was administered one week after the posttest. After the pre-test was applied to the nurses in the intervention group, five modules of training, which lasted four hours, were given using interactive methods. Five modules of training were prepared by the researcher. These five modules are the 1st module of training; definition of hemovigilance, its aims, the development of hemovigilance in the world and in Turkey, and legal legislation, Module 2; Donor selection, Blood donation Process, Phlebotomy and Donor reactions, Module 3; blood, blood transfusion, its purpose, properties of blood and blood components, Blood transfusion process, Module 4; acute and delayed transfusion reactions and management, Module 5; It consists of the national hemovigilance system, the organization of the hemovigilance system at the hospital level, Traceability, Trace-back from the Patient to the Donor, and Look-back from the Donor to the Patient. the training was over, the final test was administered. One month later, this test was repeated.

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

She/He voluntarily agrees to participate in the research, Working as a nurse in the clinic and intensive care unit where blood transfusions are the most, Working for at least 6 months,

Exclusion criteria

Nurses working in the emergency and operating rooms, in clinics where blood transfusion is not performed the most, Being a new nurse, On maternity leave and maternity leave, Having an external assignment, Nurses working in the polyclinic,

Treatment and study plan

Training

Other

Hemovigilance module training

Primary outcomes

  1. Hemovigilance Information Form

    Time frame: 5 hours or 1 month

    It consists of fifteen questions about hemovigilance and hemovigilance system and definitions.

  2. Information Form on Blood Transfusion Complications

    Time frame: 5 hours or 1 month

    This section consists of nine questions including transfusion complications.

  3. Information Form on Blood Transfusion Applications

    Time frame: 5 hours or 1 month

    This section consists of sixteen questions including donor selection, questions about blood components, blood group and safe blood transfusion.

Sponsors and collaborators

Lead sponsor

Ankara Yildirim Beyazıt University

Other

Registry information

Official study title

EVALUATION OF THE EFFICIENCY OF HEMOVIGILANCE MODULE TRAININGS

Important dates

Study start
2022
Primary completion
2022
Study completion
2022
First posted
Nov 23, 2022
Registry last updated
Nov 23, 2022

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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