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 TherapyWeb-applicationBreast 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
Name Time Method Observance of hormontherapy 18 months Evaluate the benefit of a web-based application on hormone therapy compliance (Morisky questionnary; answer Yes or No; 8 questions)
- Secondary Outcome Measures
Name Time Method Quality of life with self questionnaires 18 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, FranceFrançois GERNIER, Study nursePrincipal InvestigatorJean-Michel GRELLARD, project managerContact+ 33 2 31 45 50 50jm.grellard@baclesse.unicancer.frGaelle ANNE, Study nurseSub InvestigatorCharlotte CEINTRE, Study nurseSub InvestigatorRose-Marie CHARLES, Study nurseSub InvestigatorAudrey FAVEYRIAL, MDSub InvestigatorChristelle LEVY, MDSub InvestigatorEmile GEORGE, MDSub InvestigatorDjelila ALLOUACHE, MDSub InvestigatorJulien GEFFRELOT, MDSub InvestigatorCarine SEGURA, MDSub InvestigatorKatharina GUNZER, MDSub InvestigatorIoana HRAB, MDSub InvestigatorAlison JOHNSON, MDSub InvestigatorAdeline MOREL, MDSub Investigator