Risk Perception of Needlestick Injury

N/AUnknownNCT06199765

Hospital Universiti Sains Malaysia90 enrolled

Overview

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

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

Allocation

NON_RANDOMIZED

Purpose

PREVENTION

Masking

SINGLE

Enrollment

Conditions

Needlestick Injuries

Interventions

Needlestick Injury PreventionOTHER

this intervention will be using needlestick injury prevention module which will involve lecture, demonstration, and role play

Eligibility

Sex: ALLHealthy volunteers:

Medical Language ↔ Plain English

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

Locations (1)

Hospital Raja Perempuan Zainab II

Kota Bharu, Kelantan, Malaysia

Outcomes

Primary Outcomes

Needlestick injury Risk Perception Score

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.

Time frame: right after intervention and 4 weeks after

Data from ClinicalTrials.gov

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