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Effectiveness of Education Training Program in Preventing Needle Stick Injury among Healthcare Workers in Health Clinics in Kuala Lumpur.

Effectiveness of Education Training Program in Preventing Needle Stick Injury among Healthcare Workers in Health Clinics in Kuala Lumpur.

Status
Not yet recruiting
Phases
Unknown
Study type
Interventional
Source
ANZCTR
Registry ID
ACTRN12617001062314
Enrollment
1440
Registered
2017-07-20
Start date
2017-07-24
Completion date
Unknown
Last updated
2017-08-21

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

None listed

Brief summary

This educational training program is a cluster randomized control trial that aims to reduce the needle stick injury. The participants will be health care workers in the health clinics. Participants in this study are randomly allocated (by chance) to one of two groups. Participants in the intervention group will attend one day workshop which will include face to face lectures, group discussion and roleplays by trained peer health care workers from their clinics. The content of the training program will include knowledge on needle stick injury and its prevention strategies, blood borne diseases transmitted by needle stick injury. Participants in the control group will be on the waiting list still the study is completed and will be exposed to the usual care of training on needle stick injury conducted by the infectious control unit of their clinics. If the training workshop is effective, the control group will receive the training upon completion of the study. A self-administered questionnaire that will be validated and tested for reliability will be used to collect data from the participants. Participants from both groups will be asked to complete questionnaires before the training program begins (baseline), at 1 month, 3 month and again at 6 months, in order to determine the effect of the program on needle stick injury.

Interventions

The intervention is an educational training program that aims to reduce the needle stick injuries. The intervention will be based on the Information-Motivation-Behavioral Skills (IMB) Model. The training program will be a one day workshop that will include the face to face lectures, group discussion and role play. The work shop will be modeled based on the literature search such as the recommendation of WHO and CDC. A training of trainers will be done by the researcher who is a medical officer

The intervention is an educational training program that aims to reduce the needle stick injuries. The intervention will be based on the Information-Motivation-Behavioral Skills (IMB) Model. The training program will be a one day workshop that will include the face to face lectures, group discussion and role play. The work shop will be modeled based on the literature search such as the recommendation of WHO and CDC. A training of trainers will be done by the researcher who is a medical officer with Masters in Public Health to selected health care workers from the clinics. The selected health care workers to conduct the workshop at their clinics.The workshop will be conducted at the health clinics by healthcare workers who will be trained using a standardized training manual developed for this study. The workshop will begin with the ice breaking activity and introduction to the objectives of the workshop as well as ground rules for the participants. This will be followed by lectures to provide information on epidemiology of needle stick injury, blood borne disease and the prevention of needle stick injuries. For the motivation construct, group discussions from case scenarios. This case scenarios will be of previous true cases. Finally for the behavioral skill construct, problem solving activities based on daily practice encounters that increase needle stick injuries will be used. This will include both role plays and group discussion. The workshop will end with review of lessons learnt, take home messages and t evaluation of the workshop. Certificate of participation will be provides to the participants of the workshop.

Sponsors

Prem Kumar A Balakrishnan
Lead SponsorIndividual

Study design

Allocation
Randomised controlled trial
Intervention model
Parallel
Primary purpose
Educational / counselling / training
Masking
Blinded (masking used) (Investigator, Outcomes Assessor)

Eligibility

Sex/Gender
All
Age
21 Years to 65 Years
Healthy volunteers
Yes

Inclusion criteria

All health care workers 1.Medical officers 2.Dental officers 3.Pharmacist 4.Paramedics 5.Nurses 6.Laboratory technologist 7. Dental technicians 8. Dental nurses 9. Attendants

Exclusion criteria

Participants who are not available during the study period due to leave such as maternity and study leave.

Outcome results

None listed

Source: ANZCTR · Data processed: Feb 4, 2026