Ignite Creation Date:
2024-05-06 @ 8:25 PM
Last Modification Date:
2024-10-26 @ 3:27 PM
Study NCT ID:
NCT06371690
Status:
COMPLETED
Last Update Posted:
2024-04-17
First Post:
2023-12-30
Brief Title:
The Effects of Using the Web-Based Double Eye Control Program on Medication Error
Sponsor:
Izmir Katip Celebi University
Organization:
Izmir Katip Celebi University
Study Overview
Official Title:
The Effects of Using the Web-Based Double Eye Control Program on Medication of High Risk Drugs in Pediatric Patients The Effect of Web-Based Double Eye Control Program
Status:
COMPLETED
Status Verified Date:
2024-04
Last Known Status:
None
Delayed Posting:
No
If Stopped, Why?:
Not Stopped
Has Expanded Access:
False
If Expanded Access, NCT#:
N/A
Has Expanded Access, NCT# Status:
N/A
Acronym:
None
Brief Summary:
Methods The study was carried out as a quasi-experimental study in the Pediatric Surgery Clinics of a university hospital using the Pre-Test-Post-Test Model in a Single Group The sample of the study consisted of all high-risk drugs administered by 24 nurses working in these clinics taking part in medication and agreeing to take part in the study Data were collected by the researcher using the Medication Observation Form The Form was created based on the literature and by making use of the 10 Correct Rules in Medication and the Medication Skills Steps in the Double Eye Control Program In the first step medication error rates were determined through observation method In the second step the Web-Based Double-Eye Control Program which is a standard drug dose calculation and medication program created by the researchers was started to be implemented Medication error rates were determined again through post-intervention observation method Informed voluntary consent ethics committee and hospital permissions were obtained for the implementation of the study
Detailed Description:
Background In this study it was aimed to examine the effect of using Web Based Double-Eye Control Program as a new decision support system in preventing errors and standardization in high-risk medications of pediatric nurses
Methods The study was carried out as a quasi-experimental study in the Pediatric Surgery Clinics of a university hospital using the Pre-Test-Post-Test Model in a Single Group The sample of the study consisted of all high-risk drugs 532 before the intervention 538 after the intervention a total of 1070 drug doses administered by 24 nurses working in these clinics taking part in medication and agreeing to take part in the study Data were collected by the researcher using the Medication Observation Form The Form was created based on the literature and by making use of the 10 Correct Rules in Medication and the Medication Skills Steps in the Double Eye Control Program In the first step medication error rates were determined through observation method In the second step the Web-Based Double-Eye Control Program which is a standard drug dose calculation and medication program created by the researchers was started to be implemented Medication error rates were determined again through post-intervention observation method Informed voluntary consent ethics committee and hospital permissions were obtained for the implementation of the study
Methods The study was carried out as a quasi-experimental study in the Pediatric Surgery Clinics of a university hospital using the Pre-Test-Post-Test Model in a Single Group The sample of the study consisted of all high-risk drugs 532 before the intervention 538 after the intervention a total of 1070 drug doses administered by 24 nurses working in these clinics taking part in medication and agreeing to take part in the study Data were collected by the researcher using the Medication Observation Form The Form was created based on the literature and by making use of the 10 Correct Rules in Medication and the Medication Skills Steps in the Double Eye Control Program In the first step medication error rates were determined through observation method In the second step the Web-Based Double-Eye Control Program which is a standard drug dose calculation and medication program created by the researchers was started to be implemented Medication error rates were determined again through post-intervention observation method Informed voluntary consent ethics committee and hospital permissions were obtained for the implementation of the study
Study Oversight
Has Oversight DMC:
None
Is a FDA Regulated Drug?:
False
Is a FDA Regulated Device?:
False
Is an Unapproved Device?:
None
Is a PPSD?:
None
Is a US Export?:
None
Is an FDA AA801 Violation?:
None