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

NCT ID: NCT04554927

Last Updated: 2025-09-22

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

RECRUITING

Clinical Phase

NA

Total Enrollment

438 participants

Study Classification

INTERVENTIONAL

Study Start Date

2020-09-03

Study Completion Date

2025-12-31

Brief Summary

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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

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Conditions

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Web-application Breast Cancer Hormono Therapy

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Primary Study Purpose

OTHER

Blinding Strategy

NONE

Study Groups

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WEB-application

Group Type EXPERIMENTAL

WEB-Application

Intervention Type OTHER

The patients of the Web-application arm will be trained on the devices and the application will be installed either on their smartphone or on another support (computer, tablet).

Standard accompaniment

Group Type ACTIVE_COMPARATOR

Standard accompaniment

Intervention Type OTHER

Personalized schedule of medical follow-up given to the patient

Interventions

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WEB-Application

The patients of the Web-application arm will be trained on the devices and the application will be installed either on their smartphone or on another support (computer, tablet).

Intervention Type OTHER

Standard accompaniment

Personalized schedule of medical follow-up given to the patient

Intervention Type OTHER

Eligibility Criteria

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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
Minimum Eligible Age

18 Years

Eligible Sex

FEMALE

Accepts Healthy Volunteers

No

Sponsors

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Centre Francois Baclesse

OTHER

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Locations

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Centre François baclesse

Caen, , France

Site Status RECRUITING

Countries

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France

Facility Contacts

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François GERNIER, Study nurse

Role: primary

+ 33 2 31 45 50 50

Jean-Michel GRELLARD, project manager

Role: backup

+ 33 2 31 45 50 50

References

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Gernier F, Grellard JM, Dupont C, Castel H, Fernette M, Lahaye F, Charles RM, Leroux T, Ory C, Faveyrial A, Morel A, Emile G, Levy C, Segura C, Allouache D, Johnson A, Geffrelot J, Gunzer K, Lelaidier A, Girault G, Dubot-Poitelon C, San C, Lequesne J, Clarisse B. Impact of web application support versus standard management on adherence with adjuvant hormone therapy in patients treated for breast cancer: the WEBAPPAC study. BMC Cancer. 2023 Aug 9;23(1):736. doi: 10.1186/s12885-023-11242-1.

Reference Type DERIVED
PMID: 37559004 (View on PubMed)

Other Identifiers

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WEBAPPAC

Identifier Type: -

Identifier Source: org_study_id

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