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Recruiting NCT06726889

Increasing Oral Medication Adherence for Metastatic Breast Cancer Patients

Trial Parameters

Condition Breast Cancer
Sponsor European Institute of Oncology
Study Type OBSERVATIONAL
Phase N/A
Enrollment 104
Sex ALL
Min Age 18 Years
Max Age N/A
Start Date 2024-01-25
Completion 2025-04
Interventions
Standard careDecision Support System (DSS)Reminders

Brief Summary

Aim of this study is to optimize an adherence increasing intervention designed for metastatic Breast Cancer (BC) patients by applying a full factorial design in order to evaluate the optimal combination of three different intervention components.

Eligibility Criteria

Inclusion Criteria: * Patients with a diagnosis of metastatic BC * Patients with a prescription for any OAA (i.e. oral chemotherapy, endocrine therapy, and Cyclin-Dependent Kinase 4/6 Inhibitors) * Age \>18 years old * Patients with a personal smart phone with internet access * Willingness and ability to comply with scheduled visits and other trial procedures * Understanding and speaking Italian language * Written informed consent Exclusion Criteria: * Psychiatric disorders or conditions that might impair the ability to give informed consent * Comorbidity that may impact on compliance to study procedures

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