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Clinical Trial Details — Status: Active, not recruiting

Administrative data

NCT number NCT06199765
Other study ID # NMRR ID-23-00281-VRX
Secondary ID
Status Active, not recruiting
Phase N/A
First received
Last updated
Start date November 19, 2023
Est. completion date January 11, 2024

Study information

Verified date January 2024
Source Hospital Universiti Sains Malaysia
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

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


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.


Recruitment information / eligibility

Status Active, not recruiting
Enrollment 90
Est. completion date January 11, 2024
Est. primary completion date November 26, 2023
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group N/A and older
Eligibility 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


Related Conditions & MeSH terms


Intervention

Other:
Needlestick Injury Prevention
this intervention will be using needlestick injury prevention module which will involve lecture, demonstration, and role play

Locations

Country Name City State
Malaysia Hospital Raja Perempuan Zainab II Kota Bharu Kelantan

Sponsors (1)

Lead Sponsor Collaborator
Hospital Universiti Sains Malaysia

Country where clinical trial is conducted

Malaysia, 

Outcome

Type Measure Description Time frame Safety issue
Primary 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
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