A Qualitative Study on Treatment Adherence in Patients With Metastatic Breast Cancer
1 other identifier
observational
20
1 country
1
Brief Summary
Qualitative observational study with the aim to explore medication adherence in a sample of patients with metastatic breast cancer. Patients with metastatic breast cancer receiving or having received oral oncologic therapy, and attending the Division of Medical Senology at the European Institute of Oncology, will be included and enrolled in this research project."
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at below P25 for all trials
Started Oct 2022
Typical duration for all trials
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
Study Start
First participant enrolled
October 3, 2022
CompletedFirst Submitted
Initial submission to the registry
March 26, 2024
CompletedFirst Posted
Study publicly available on registry
April 2, 2024
CompletedPrimary Completion
Last participant's last visit for primary outcome
December 31, 2024
CompletedStudy Completion
Last participant's last visit for all outcomes
December 31, 2024
CompletedApril 2, 2024
March 1, 2024
2.2 years
March 26, 2024
March 26, 2024
Conditions
Outcome Measures
Primary Outcomes (1)
Evaluation of factors influencing patients' adherence to medical therapy
Collection of data in order to evaluation of factors influencing patient's adherence to medical treatment
1 month
Study Arms (1)
Metastatic breast cancer (BC)
Patients with diagnosis of BC
Eligibility Criteria
Patients with diagnosis of metastatic breast cancer treated at European Institute of Oncology
You may qualify if:
- Age over 18 years old;
- Diagnosis of metastatic breast cancer;
- Availability of an internet connection and a PC or Tablet (for remote focus groups);
- Signing of the informed consent.
You may not qualify if:
- Presence of psychiatric or neurological conditions impairing the ability to comprehend the questions in Focus Groups or to express free consent to participate in the study;
- Presence of medical or oncological conditions other than metastatic breast cancer;
- Refusal to sign the informed consent.
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
European Institute of Oncology
Milan, Italy
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Officials
- PRINCIPAL INVESTIGATOR
Gabriella Pravettoni
European Institute of Oncology
Central Study Contacts
Study Design
- Study Type
- observational
- Observational Model
- CASE ONLY
- Time Perspective
- PROSPECTIVE
- Sponsor Type
- OTHER
- Responsible Party
- SPONSOR
Study Record Dates
First Submitted
March 26, 2024
First Posted
April 2, 2024
Study Start
October 3, 2022
Primary Completion
December 31, 2024
Study Completion
December 31, 2024
Last Updated
April 2, 2024
Record last verified: 2024-03