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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.
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| 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. |
|
| 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. |
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| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| Needlestick Injury Prevention | Other | this intervention will be using needlestick injury prevention module which will involve lecture, demonstration, and role play |
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| Measure | Description | Time Frame |
|---|---|---|
| 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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Inclusion Criteria:
Exclusion Criteria:
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| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| Hospital Raja Perempuan Zainab II | Kota Bharu | Kelantan | 16150 | Malaysia |
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| ID | Term |
|---|---|
| D016602 | Needlestick Injuries |
| ID | Term |
|---|---|
| D014951 | Wounds, Stab |
| D014950 | Wounds, Penetrating |
| D014947 | Wounds and Injuries |
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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.
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Control group will be given materials regarding patient safety as masking. Patient safety will have some element on needlestick and injury prevention.