Actively Recruiting
Adherence and Understanding of a Therapeutic Education Program for Patients With Central Venous Access (EDUVVC)
Led by Assistance Publique - Hôpitaux de Paris · Updated on 2024-10-18
100
Participants Needed
1
Research Sites
58 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
The aim of this project is to evaluate, in a prospective cohort of PICC line patients, adherence to the project and understanding of the messages. The transmission of knowledge and the acquisition of skills by patients with this type of invasive device will enable them to play an active role in their own care, and could help to reduce the frequency of risks. This project is part of a collaborative approach that includes the creation of a mobile application for therapeutic education and monitoring (application under development). The evaluation of the device will be the subject of a national PHRC with national structures (SPIADI and PRIMO). The aim is to create a city-hospital collaboration to improve risk management.
CONDITIONS
Official Title
Adherence and Understanding of a Therapeutic Education Program for Patients With Central Venous Access (EDUVVC)
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Adult patients over 18 years of age
- Patients requiring a PICC line
- Patients with a means of communication with an Internet connection (computer or cell phone) or an alternative solution (landline telephone)
- Patients with a predicted life expectancy of more than 6 weeks
You will not qualify if you...
- Patient opposed to participating in the study
- Patient does not understand French
- Patient not affiliated to a French social security scheme
- Patient under guardianship or curatorship
- Patient under court protection
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 1 location
1
Hopital Avicenne
Bobigny, France, 93000
Actively Recruiting
Research Team
C
Camille REINPRECHT
CONTACT
Z
Zahar Jean Ralph, PUPH
CONTACT
How is the study designed?
Study Type
OBSERVATIONAL
Masking
N/A
Allocation
N/A
Model
N/A
Primary Purpose
N/A
Number of Arms
0
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