Structured Training on Oncology Nurses' Performance Related Port A Cath Device

November 11, 2023 updated by: Heba Abubakr Mohamed Salama, Mansoura University

Effect of a Structured Simulation-based Training on Oncology Nurses' Performance Regarding Port A Cath Device.

evaluate the effect of structured simulation-based training on oncology nurses' performance regarding port A cath device.

Study Overview

Status

Completed

Conditions

Intervention / Treatment

Detailed Description

All oncology nurses who are expected to deal with port a-cath device will be recruited in the study pre test will introduced first, then simulated based training will be placed related to port a-cath device care after that , post test will be done immediately and 3 months later to measure nurses knowledge and practice level

Study Type

Interventional

Enrollment (Actual)

50

Phase

  • Not Applicable

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

  • Egypt
      • Mansoura, Egypt
        • Heba Abubakr Salama

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

  • Child
  • Adult
  • Older Adult

Accepts Healthy Volunteers

Yes

Description

Inclusion Criteria:

  • Oncology nurses who are providing direct care for patients with port a-cath device

Exclusion Criteria:

  • Participants who will not be able to complete the questionnaire

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Primary Purpose: Supportive Care
  • Allocation: N/A
  • Interventional Model: Single Group Assignment
  • Masking: None (Open Label)

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Experimental: Nurses
A simulation-based training will be done for all nurses
Behavioral: simulation-based training
the training will include a theoretical & practical parts

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
change in oncology nurses' knowledge and practice regarding port a-cath device care
Time Frame: 3 months

The researchers will provide a structured questionnaire based on reviewing related literatures called "Port a-Cath Nurses Knowledge questionnaire", it will consist of closed-ended questions to assess Nurses Knowledge And they will assess Nurses Practice level by using the preprepared Port a-Cath Nurses observational checklist.

They will be used three times: before, immediately after training and 3 months post training
3 months

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Sponsor

Mansoura University

Investigators

  • Study Chair: faculty of Nursing, Mansoura University

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

March 15, 2023

Primary Completion (Actual)

June 1, 2023

Study Completion (Actual)

June 30, 2023

Study Registration Dates

First Submitted

March 2, 2023

First Submitted That Met QC Criteria

March 15, 2023

First Posted (Actual)

March 17, 2023

Study Record Updates

Last Update Posted (Actual)

November 15, 2023

Last Update Submitted That Met QC Criteria

November 11, 2023

Last Verified

November 1, 2023

More Information

Terms related to this study

Keywords

Additional Relevant MeSH Terms

Other Study ID Numbers

  • training on port A cath device

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

NO

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

Clinical Trials on Port a Cath

Clinical Trials on simulation-based training

Search Similar Trials

Sponsors and Collaborators

Medical Conditions

Drug Interventions

CROs by country

CROs in Cote d'Ivoire

Conditions

Rare Diseases

Drug Interventions

Dietary Supplements

Sponsor/Collaborators

Locations

Subscribe