Multidisciplinary Care Pathway With Electronic Patient Reported Outcomes (ePRO) Post-operative Follow-up of Breast Cancer Surgery Complications to Optimize Patient Quality of Life

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Description

This project is a follow-on study of the BEAUTIFY-2 study (NCT04957186). The "BEAUTIFY" (BrEast cAncer qUaliTy of lIfe aFter surgerY) program was built by a committee of experts on the basis of reflections carried out within 2 focus groups. An application was developed to track patient reported outcome measures.

The study investigators now wish to evaluate the feasibility and impact on pain and quality of life of the "BEAUTIFY" care pathway on a larger cohort. The study hypothesis is that multidisciplinary care organization will improve the management and the quality of life post-breast cancer surgery.

Targeted Conditions

Study Overview

Start Date
July 25, 2022
Completion Date
July 1, 2024
Enrollment
50
Date Posted
July 8, 2022
Accepts Healthy Volunteers?
No
Gender
Female

Locations

Full Address
CHU de Nîmes
Nîmes, France

Eligibility

Minimum Age (years)
18
Eligibility Criteria
Inclusion Criteria:

Breast cancer patient scheduled for surgery
Patient able to use a connected electronic object and having a tablet or a smartphone with internet access at home.
The patient must have given their free and informed consent and signed the consent form
The patient must be a member or beneficiary of a health insurance plan

Exclusion Criteria:

The subject is participating in a category 1 interventional study, or is in a period of exclusion determined by a previous study
The subject unable to express consent
It is impossible to give the subject informed information
The patient is under safeguard of justice or state guardianship

Study Contact Info

Study Contact Name
Frédéric Fiteni
Study Contact Email
Study Contact Phone

Contact Listings Owner Form

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Other Details

FDA Regulated Drug?
No
FDA Regulated Device?
No
NCTid (if applicable)
NCT05449340