Risk Perception of Needlestick Injury

NCT06199765 | Unknown

• 1 other identifier: NMRR ID-23-00281-VRX
• Study Type: interventional
• Target: 90
• Locations: 1 country
• Sites: 1

Brief Summary

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

Conditions

Needlestick Injuries

Outcome Measures

Primary Outcomes (1)

• 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.

  right after intervention and 4 weeks after

Study Arms (2)

Lecture, demonstration, and role play on NSI

EXPERIMENTAL

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

Patient Safety Materials

SHAM COMPARATOR

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

Interventions

Needlestick Injury Prevention OTHER

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

Lecture, demonstration, and role play on NSI; Patient Safety Materials

Eligibility Criteria

• Sex: all
• Healthy Volunteers: Yes
• Age Groups: Child (0-17), Adult (18-64), Older Adult (65+)

You may qualify if:

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

You may not qualify if:

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

Sponsors & Collaborators

• Hospital Universiti Sains Malaysia: lead

Study Sites (1)

Hospital Raja Perempuan Zainab II

Kota Bharu, Kelantan, 16150, Malaysia

Location

MeSH Terms

Conditions

Needlestick Injuries

Condition Hierarchy (Ancestors)

Wounds, Stab; Wounds, Penetrating; Wounds and Injuries

Study Design

• Study Type: interventional
• Phase: not applicable
• Allocation: NON RANDOMIZED
• Masking: SINGLE
• Who Masked: PARTICIPANT
• Masking Details: Control group will be given materials regarding patient safety as masking. Patient safety will have some element on needlestick and injury prevention.
• Purpose: PREVENTION
• Intervention Model: PARALLEL
• Sponsor Type: OTHER
• Responsible Party: PRINCIPAL INVESTIGATOR
• PI Title: Doctor

Model Details: All house officers who were eligible and consented, who participated in cross sectional study were included into intervention group until the required sample size was achieved. The same numbers of officers, eligible and consented were included into control group. For intervention, only educational intervention will be given which consist of lecture, demonstration, and role play. After that, data collection will be given right after the intervention completion and 4 weeks after that using self administered questionnaire. The same will be applied to the control group which data collection will be done right masking and 4 weeks later.

Study Record Dates

• First Submitted: December 28, 2023
• First Posted: January 10, 2024
• Study Start: November 19, 2023
• Primary Completion: November 26, 2023
• Study Completion: January 11, 2024
• Last Updated: January 17, 2024

Record last verified: 2024-01

Data Sharing

• IPD Sharing: Will not share

Locations

MY (1)