RecruitingPhase 3NCT06781996

A Study to Determine the Efficacy of a Digital Self-management Support Tool to Improve the Quality of Life During Adjuvant HOrmonal Therapy for Patients With Early Breast Cancer

Phase III Randomized Controlled Open Label Clinical Trial to Determine the Efficacy of a Digital Self-management Support Tool to Improve the Quality of Life During Adjuvant HOrmonal Therapy for Patients With Early Breast Cancer


Sponsor

Gustave Roussy, Cancer Campus, Grand Paris

Enrollment

180 participants

Start Date

Sep 9, 2025

Study Type

INTERVENTIONAL

Conditions

Summary

Randomized trial that compares a personalized digitally-enabled pathway delivered by a mobile application in addition to standard of care vs. standard of care alone in patients with HR+ early breast cancer reporting endocrine therapy related adverse events. The HOPE study is a national, prospective, randomized, open-label trial conducted in France. 180 patients will be randomly assigned 1:1 to receive either 12 weeks of multimodal Resilience© digital companion including education and self-care modules in addition to the standard of care provided by their treating oncologists and supportive care team at their care centers or 12 weeks of standard of care provided by their treating oncologists and supportive care team at their care centers. Data from the literature in oncology trials with Patient-Reported Outcomes suggests that in the absence of double-blind concealment, clinically important differences could still be detected.


Eligibility

Min Age: 18 Years

Plain Language Summary

Simplified for easier understanding

This study is testing whether a digital smartphone app can help women with hormone receptor-positive breast cancer better manage the side effects of hormone therapy (such as hot flashes, joint pain, and fatigue), which are a major reason women stop taking these important medications. **You may be eligible if...** - You are 18 or older - You have stage I–III hormone receptor-positive breast cancer - You are currently taking hormone therapy (tamoxifen or an aromatase inhibitor) - You own a smartphone - You are experiencing side effects from your hormone therapy **You may NOT be eligible if...** - Your breast cancer has spread to other parts of the body - You are not currently on hormone therapy Talk to your doctor to see if this trial is right for you.

This summary was AI-generated to explain the trial in plain language. It is not medical advice. Always discuss eligibility with your doctor before enrolling in a clinical trial.

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Interventions

OTHERmultimodal Resilience© digital companion

Resilience© is a multi-component, multi-level interventional mobile application that will offer: (a) supportive educational care information (b) self-symptom management resources with availability of a remote health-care provider evaluation that addresses patient-specific needs in survivorship care and recommends personalized digital self-management resources at onboarding and if needed in case of low engagement in the mobile app. Intervention duration : 3 weeks

OTHERStandard supportive care

standard of care provided by the oncologist and supportive care team at the patient local cancer center including referrals for local supportive care programs. Local supportive care programs may also include the use of already deployed remote patient monitoring and solutions, digital and in person education.


Locations(1)

Gustave Roussy

Villejuif, France

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NCT06781996


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