Safer Use of Medication in Pediatric Patients at Home

NCT04598139 | Unknown

• 1 other identifier: PI18/00739
• Study Type: observational
• Target: 62
• Locations: 1 country
• Sites: 1

Brief Summary

This study aims:

• to develop a web-based notification system for caregivers of pediatric patients that allows to report medication errors and, based on this notification, and to share experiences and alerts about common errors of patients.
• to assess de user satisfaction and perceived usefulness of the system. Participants: Parents with children who have required drug treatment in the last two months, who have an Internet connection and who agree to participate in the study. Sample size: 62 participants Main outcome variable: overall satisfaction

Conditions

Medication Errors and Other Product Use Errors and Issues

Outcome Measures

Primary Outcomes (1)

• Satisfaction with the web-based medication error notification system

  Overall satisfaction with the web-based medication error notification system by an ad hoc questionnaire

  At one month after use of the website

Study Arms (1)

Study group

Other: Study group

Interventions

Study group OTHER

The study group uses a web-based medication error notification system

Study group

Eligibility Criteria

• Age: 18 Years - 80 Years
• Sex: all
• Healthy Volunteers: Yes
• Age Groups: Adult (18-64), Older Adult (65+)
• Sampling Method: Non-Probability Sample

Study Population

Parents or caregivers of children aged from 0 to 14 years.

You may qualify if:

• To care children aged under 14 years who have required drug treatment in the last two months
• To have an Internet connection
• To agree to participate in the study.
• To be registered in the study web-based notification system
• Age \> 17 years

You may not qualify if:

• To be health provider
• To care children in residence for minors.
• To care children with a life expectancy of less than 2 years.

Sponsors & Collaborators

• Universidad Miguel Hernandez de Elche: lead

Study Sites (1)

Mercedes Gilabert

Elche, Alicante, 03202, Spain

Location

Study Design

• Study Type: observational
• Observational Model: OTHER
• Time Perspective: CROSS SECTIONAL
• Sponsor Type: OTHER
• Responsible Party: PRINCIPAL INVESTIGATOR
• PI Title: Principal investigator

Study Record Dates

• First Submitted: October 8, 2020
• First Posted: October 22, 2020
• Study Start: May 5, 2021
• Primary Completion: December 31, 2022
• Study Completion: December 31, 2022
• Last Updated: May 18, 2022

Record last verified: 2022-05

Locations

ES (1)