Risk Perception of Needlestick Injury

January 13, 2024 updated by: Ahmed Farrasyah Bin Mohd Kutubudin, Hospital Universiti Sains Malaysia

Predictors of Perception on Risk of Needlestick Injury and Effectiveness of The Needlestick Prevention Module Among House Officers in Kelantan

The purpose of this study is to determine the effectiveness of needlestick injury prevention module

Study Overview

Status

Active, not recruiting

Conditions

Intervention / Treatment

Detailed Description

After being informed about the study and the potential risk, participants were given written informed consent to be filled out and signed. Agreed participants will receive a 1-week duration of educational intervention. The intervention only involved education and was less likely to cause injury or damage to the body.

Study Type

Interventional

Enrollment (Estimated)

90

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

  • Malaysia
    • Kelantan
      • Kota Bharu, Kelantan, Malaysia, 16150
        • Hospital Raja Perempuan Zainab II

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:

  1. All house officer in government hospitals with house officer training programme
  2. House officers must be among those who join housemanship program for minimum of 1 month duration

Exclusion Criteria:

  1. House officer who undergo attachment outside the training hospital
  2. House officer that are not available during the data collection period or on long leave

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: Prevention
  • Allocation: Non-Randomized
  • Interventional Model: Parallel Assignment
  • Masking: Single

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Experimental: Lecture, demonstration, and role play on NSI
this arm will receive intervention regarding needlestick prevention using needlestick prevention educational module. this intervention only involve educational intervention which consist of lecture, demonstration, and role play. This intervention will be done for 1 week duration.
Other: Needlestick Injury Prevention
this intervention will be using needlestick injury prevention module which will involve lecture, demonstration, and role play
Sham Comparator: Patient Safety Materials
This arm will receive material regarding patient safety. this material will have some element of needlestick and injury prevention. this intervention will done for 1 week.
Other: Needlestick Injury Prevention
this intervention will be using needlestick injury prevention module which will involve lecture, demonstration, and role play

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Needlestick injury Risk Perception Score
Time Frame: right after intervention and 4 weeks after
determine the risk perception score improvement using likert scale. 1 is the lowest and 5 is the highest mark. the higher the mark the better.
right after intervention and 4 weeks after

Collaborators and Investigators

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

Sponsor

Hospital Universiti Sains Malaysia

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)

November 19, 2023

Primary Completion (Actual)

November 26, 2023

Study Completion (Estimated)

January 11, 2024

Study Registration Dates

First Submitted

December 28, 2023

First Submitted That Met QC Criteria

December 28, 2023

First Posted (Actual)

January 10, 2024

Study Record Updates

Last Update Posted (Actual)

January 17, 2024

Last Update Submitted That Met QC Criteria

January 13, 2024

Last Verified

January 1, 2024

More Information

Terms related to this study

Additional Relevant MeSH Terms

Other Study ID Numbers

  • NMRR ID-23-00281-VRX

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.

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