Adherence and Understanding of a Therapeutic Education Program for Patients With Central Venous Access (EDUVVC)

NCT06478849 | Completed

• 1 other identifier: APHP231313
• Study Type: observational
• Target: 105
• Locations: 1 country
• Sites: 1

Brief Summary

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

Therapeutic Education Program; Prevention

Keywords

central venous line

Outcome Measures

Primary Outcomes (1)

• Assess patients' level of understanding of communication tools.

  The level of comprehension will be assessed on the acquisition of the main messages and will be expressed as a percentage of correct answers.

  WEEK 6 POST INCLUSION

Secondary Outcomes (2)

• Estimating patient adherence to communication tools

  WEEK 6 POST INCLUSION

• Identify individual factors : a- Demographic b- Related to underlying pathology c- Management-related

  week 6 post inclusion

Interventions

QUESTIONNAIRES OTHER

QUESTINNAIRES / WEBINARS

Also known as: WEBINARS

Eligibility Criteria

• Age: 18 Years+
• Sex: all
• Healthy Volunteers: No
• Age Groups: Adult (18-64), Older Adult (65+)
• Sampling Method: Probability Sample

Study Population

Adult patients with recent PICC line insertion, followed at AVICENNE hospital.

You may qualify if:

• 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 may not qualify if:

• 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

Sponsors & Collaborators

• Assistance Publique - Hôpitaux de Paris: lead

Study Sites (1)

Hopital Avicenne

Bobigny, 93000, France

Location

MeSH Terms

Interventions

Surveys and Questionnaires

Intervention Hierarchy (Ancestors)

Data Collection; Epidemiologic Methods; Investigative Techniques; Health Care Evaluation Mechanisms; Quality of Health Care; Health Care Quality, Access, and Evaluation; Public Health; Environment and Public Health

Study Officials

• CAMILLE REINPRECHT

  Hopital AVICENNE

  PRINCIPAL INVESTIGATOR

Study Design

• Study Type: observational
• Observational Model: COHORT
• Time Perspective: PROSPECTIVE
• Sponsor Type: OTHER
• Responsible Party: SPONSOR

Study Record Dates

• First Submitted: June 3, 2024
• First Posted: June 27, 2024
• Study Start: September 6, 2024
• Primary Completion: November 10, 2025
• Study Completion: November 10, 2025
• Last Updated: June 11, 2026

Record last verified: 2025-10

Data Sharing

• IPD Sharing: Will not share

Locations

FR (1)