Metastatic Breast Cancer Clinical Trial
Official title:
Enhancing Therapy Adherence Among Metastatic Breast Cancer Patients: the Study Protocol
NCT number | NCT06161181 |
Other study ID # | IEO1907 |
Secondary ID | |
Status | Recruiting |
Phase | N/A |
First received | |
Last updated | |
Start date | May 3, 2023 |
Est. completion date | December 30, 2023 |
Background: Emerging evidence indicates that patients with advanced cancer, such as those with MBC, often exhibit significant levels of nonadherence to oral anticancer treatments. Leveraging of the machine learning models in clinical practice enables the provision of personalized predictions on medication adherence for individual patients, thereby supporting adherence and facilitating targeted interventions. Objective: The current protocol aims to assess the efficacy of the DSS, a web-based solution named TREAT (TREatment Adherence SupporT), and a machine learning web application in promoting adherence to oral anticancer treatments within a sample of MBC patients. Methods and Design: This protocol is part of a project titled "Enhancing Therapy Adherence Among Metastatic Breast Cancer Patients" (Tracking Number 65080791). A sample of 100 MBC patients is enrolled consecutively and admitted to the Division of Medical Senology of the European Institute of Oncology. 50 MBC patients receive the DSS for three months (experimental group), while 50 MBC patients not subjected to the intervention receive standard medical advice (control group). The protocol foresees three assessment time points: T1 (1-Month), T2 (2-Month), and T3 (3-Month). At each time point, participants fill out a set of self-reports evaluating adherence, clinical, psychological, and QoL variables. Conclusions: our results will inform about the effectiveness of the DSS and risk-predictive models in fostering adherence to oral anticancer treatments in MBC patients.
Status | Recruiting |
Enrollment | 100 |
Est. completion date | December 30, 2023 |
Est. primary completion date | December 30, 2023 |
Accepts healthy volunteers | No |
Gender | Female |
Age group | 18 Years and older |
Eligibility | Inclusion Criteria: - Patients > 18 years-old; - Having a metastatic breast cancer diagnosis; - Taking oral treatment intervention for metastatic breast cancer; - Patients with internet access and a personal smartphone or tablet; - Patients who have read and signed the informed consent. Exclusion Criteria: - Presence of primary psychiatric or neurological conditions; - Patients who refused to sign the informed consent. |
Country | Name | City | State |
---|---|---|---|
Italy | European Institute fo Oncology | Milan | MI |
Lead Sponsor | Collaborator |
---|---|
European Institute of Oncology | Pfizer |
Italy,
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* Note: There are 27 references in all — Click here to view all references
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Decision Support System Effectiveness | Evaluating the effectiveness of the DSS web-based solution and machine learning web application (TREAT - "TREatment Adherence SupporT") in fostering adherence to oral anticancer treatments | 3 Months | |
Secondary | Clinical, Psychological and Quality of Life Predictors of Adherence | Identify clinical factors (comorbidities, pain presence, tumor type, treatment type), psychological parameters (personality traits, anxiety, depression, self-efficacy for coping with cancer and sense of coherence), and QoL variables that serve as predictors for patients' adherence to OATs. | 3 Months | |
Secondary | Psychological Predictors of Adherence | Evaluate risk perception using visual analogue scale that serve as predictors for patients' adherence to OATs. | 3 Months |
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