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Impact of Web Application Support Versus Standard Management on Compliance With Adjuvant Hormone Therapy at 18 Months in Patients Treated for Breast Cancer

Not Applicable
Recruiting
Conditions
Hormono Therapy
Web-application
Breast Cancer
Registration Number
NCT04554927
Lead Sponsor
Centre Francois Baclesse
Brief Summary

The investigators hypothesize that the implementation of a Web-application in patients initiating adjuvant hormone therapy for breast cancer brings a benefit on treatment adherence and quality of life.

Detailed Description

Not available

Recruitment & Eligibility

Status
RECRUITING
Sex
Female
Target Recruitment
438
Inclusion Criteria
  • Patient > 18 years old
  • Breast cancer patient candidate for adjuvant hormone therapy
  • Mastery of the French language
  • Patient with a cell phone and an Internet connection
  • Patient able to use a computer, smartphone, or tablet.
  • Patient affiliated to a social security system
  • Signing of informed consent prior to any specific study-related procedure
Exclusion Criteria
  • Patient who has previously received hormone therapy for cancer.
  • Patient not trained in the use of the application
  • Any associated medical or psychiatric condition that might compromise the patient's ability to participate in the study
  • Patients with locoregional or metastatic recurrence
  • Other history of cancer.
  • Patient deprived of liberty, under guardianship or curatorship
  • Simultaneous participation in a therapeutic clinical trial or other clinical study involving a connected tool
  • Patient unable to undergo trial follow-up for geographical, social or psychopathological reasons

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Primary Outcome Measures
NameTimeMethod
Observance of hormontherapy18 months

Evaluate the benefit of a web-based application on hormone therapy compliance (Morisky questionnary; answer Yes or No; 8 questions)

Secondary Outcome Measures
NameTimeMethod
Quality of life with self questionnaires18 months

uality of life scores according (EORTC QLQ-BR23 self-questionnaires ; minimum not at all to maximum Lot; 23 questions)

Trial Locations

Locations (1)

Centre François baclesse

🇫🇷

Caen, France

Centre François baclesse
🇫🇷Caen, France
François GERNIER, Study nurse
Principal Investigator
Jean-Michel GRELLARD, project manager
Contact
+ 33 2 31 45 50 50
jm.grellard@baclesse.unicancer.fr
Gaelle ANNE, Study nurse
Sub Investigator
Charlotte CEINTRE, Study nurse
Sub Investigator
Rose-Marie CHARLES, Study nurse
Sub Investigator
Audrey FAVEYRIAL, MD
Sub Investigator
Christelle LEVY, MD
Sub Investigator
Emile GEORGE, MD
Sub Investigator
Djelila ALLOUACHE, MD
Sub Investigator
Julien GEFFRELOT, MD
Sub Investigator
Carine SEGURA, MD
Sub Investigator
Katharina GUNZER, MD
Sub Investigator
Ioana HRAB, MD
Sub Investigator
Alison JOHNSON, MD
Sub Investigator
Adeline MOREL, MD
Sub Investigator

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