Needlestick InjuriesNCT06199765
Risk Perception of Needlestick Injury
A study testing Needlestick Injury Prevention in people with Needlestick Injuries, run by Hospital Universiti Sains Malaysia at 1 site in Malaysia.
Trial summary
The purpose of this study is to determine the effectiveness of needlestick injury prevention module Read more about this study
- Who is it for?
- Any ageHealthy volunteers can take part
- Conditions the study is for
- Needlestick Injuries
- What is being tested?
- Needlestick Injury Prevention
- Could I receive a placebo?
- Yes, some participants may receive a placebo
- How many people
- 90 participants
- Where
- 1 siteMalaysia
- Study dates
- 19 Nov 2023to 11 Jan 2024
- Phase
- Interventional
- Are there results?
- None posted in the registry
Key requirements
Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.
- Ages Any age
- All sexes
- Healthy volunteers accepted
- Child, Adult, Older adult
Who may be able to join
- 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
Who cannot join
- House officer who undergo attachment outside the training hospital
- House officer that are not available during the data collection period or on long leave
Trial locations and contacts
1 site in 1 country.
About this study
Official title: Predictors of Perception on Risk of Needlestick Injury and Effectiveness of The Needlestick Prevention Module Among House Officers in Kelantan
The purpose of this study is to determine the effectiveness of needlestick injury prevention module
Read the 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.
- Conditions
- Needlestick Injuries
- Being tested
- Needlestick Injury Prevention
- Medical subject headings
- Needlestick Injuries
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
Needlestick Injury PreventionOther
this intervention will be using needlestick injury prevention module which will involve lecture, demonstration, and role play
| Study group | Role | What they receive |
|---|---|---|
| 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. Receives: 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. Receives: Other: Needlestick Injury Prevention |
What is being measured
The primary outcome is the main question the study is designed to answer.
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.
Measured: right after intervention and 4 weeks after
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted10 Jan 2024
- Study start19 Nov 2023
- Primary completion26 Nov 2023
- Study completion11 Jan 2024 (estimated)
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Other trials for Needlestick InjuriesStudies of the same condition, open and under way.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
More details
For doctors and researchers: how the study is designed, who runs it, and its registry IDs.
Study design
- Study type
- Interventional
- Phase
- Phase N/A
- Primary purpose
- Prevention
- Allocation
- Non-randomised
- Intervention model
- Parallel groups
- Model description
- 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.
- Masking
- Single blind
- Who is masked
- Participant
- Enrolment
- 90 participants (estimated)
Sponsor and investigators
- Lead sponsor
- Hospital Universiti Sains Malaysia
- Sponsor type
- University, hospital or other
- Responsible party
- Principal investigator, Ahmed Farrasyah Bin Mohd Kutubudin, Hospital Universiti Sains Malaysia
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT06199765
- Sponsor's protocol ID
- NMRR ID-23-00281-VRX
- Status last verified
- Jan 2024
- First submitted
- 28 Dec 2023
- Last updated
- 17 Jan 2024
- Results posted
- No
- Data monitoring committee
- No
- FDA-regulated drug
- No
- FDA-regulated device
- No
- Individual data sharing
- No
Study at a glance
From the registry record, last updated by the sponsor on 17 Jan 2024. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- Predictors of Perception on Risk of Needlestick Injury and Effectiveness of The Needlestick Prevention Module Among House Officers in Kelantan
- ClinicalTrials.gov ID
- NCT06199765
- Acronym / sponsor ID
- NMRR ID-23-00281-VRX
- Conditions
- Needlestick Injuries
- Study type
- Interventional
- Recruitment status
- Unknown status
- Enrolment
- 90 participants (estimated)
- Lead sponsor
- Hospital Universiti Sains MalaysiaUniversity, hospital or other
- Study start
- 19 Nov 2023 (actual)
- Primary completion
- 26 Nov 2023 (actual)
- Study completion
- 11 Jan 2024 (estimated)
- First posted
- 10 Jan 2024 (actual)
- Results
- Not posted in the source record
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
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 design
- Primary purpose
- Prevention
- Allocation
- Non-randomised
- Intervention model
- Parallel groups
- Masking
- Single blind (participant)
- Number of arms
- 2
- Model description
- 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.
| Arm | Type | Receives |
|---|---|---|
| Lecture, demonstration, and role play on NSI | Experimental | Other: Needlestick Injury Preventionthis 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 | Other: Needlestick Injury PreventionThis 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. |
Who may qualify
- Sex
- All
- Healthy volunteers
- Accepted
- Age groups
- Child, Adult, Older adult
Key inclusion criteria (2 listed)
- 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
Key exclusion criteria (2 listed)
- House officer who undergo attachment outside the training hospital
- House officer that are not available during the data collection period or on long leave
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Interventions
| Intervention | Type | Arms |
|---|---|---|
| Needlestick Injury Preventionthis intervention will be using needlestick injury prevention module which will involve lecture, demonstration, and role play | Other | Lecture, demonstration, and role play on NSI, Patient Safety Materials |
Primary outcome
Needlestick injury Risk Perception Score
Time frame: 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.
Results and safety
Results are not available in the source record.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 17 Jan 2024.
- Individual participant dataSharing planned: No
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Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part. This study is not recruiting at the moment.
The record lists no contact. Use the official record to reach the sponsor.
1 site in 1 country: see every site and its status.
Questions about this trial
What is this clinical trial studying?
A study testing Needlestick Injury Prevention in people with Needlestick Injuries, run by Hospital Universiti Sains Malaysia at 1 site in Malaysia.
The full registered description is in the About this study section and the official record.
Who may be eligible to take part?
The sponsor lists 2 inclusion and 2 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.
Is this clinical trial currently recruiting?
The record says: status not confirmed, as of the sponsor's last update on 17 Jan 2024. Status can change between updates, so confirm with the study contact before making plans.
Where is the study taking place?
The record lists 1 site in Malaysia. Whether a site is taking part right now should be confirmed with that site. See every site.
What are the possible benefits and risks?
They depend on the study and the treatment, and no study can promise a benefit. Some participants in this study may receive a placebo. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.
Are results available for this study?
Results are not available in the source record.
How can a doctor refer a patient or contact the research team?
The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.
What does the primary outcome measure?
Needlestick injury Risk Perception Score (time frame: right after intervention and 4 weeks after). It is what the study was designed to measure, not a finding.
Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?
No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.
How often is this information updated?
AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 17 Jan 2024.