Risk Perception of Needlestick Injury

Not Applicable

Active, not recruiting

• Conditions: Needlestick Injuries
• Interventions: Other: Needlestick Injury Prevention

• Registration Number: NCT06199765
• Lead Sponsor: Hospital Universiti Sains Malaysia

Brief Summary

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

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 Timeline

• Study Start: 2023-11-19
• Primary Completion: 2023-11-26
• Study First Submitted: 2023-12-28
• Study First Submitted QC: 2023-12-28
• Status Verified: 2024-01
• Study First Posted: 2024-01-10
• Study Completion: 2024-01-11
• Last Update Submitted: 2024-01-13
• Last Update Posted: 2024-01-17

Recruitment & Eligibility

• Status: ACTIVE_NOT_RECRUITING
• Sex: All
• Target Recruitment: 90

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 & Design

• Study Type: INTERVENTIONAL
• Study Design: PARALLEL

Arm && Interventions

Group	Intervention	Description
Patient Safety Materials	Needlestick Injury Prevention	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.
Lecture, demonstration, and role play on NSI	Needlestick Injury Prevention	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.

Primary Outcome Measures

Name	Time	Method
Needlestick injury Risk Perception Score	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.

Trial Locations

Locations (1)

Hospital Raja Perempuan Zainab II; 🇲🇾 Kota Bharu, Kelantan, Malaysia