Breast Cancer Clinical Trial
Official title:
The Involvement of Breast Cancer Patients During Oncological Consultations. A Multi-centre Randomized Controlled Trial. The Study Protocol
The main aim of the study is to assess if a pre consultation intervention facilitates
greater participation of patients (and accompanying key persons when present) in the
consultation process by determining an increase in questioning and/or in the number of
different illness related issues (e.g. diagnosis, treatment, prognosis) being discussed with
the oncologist.
Other aims are to assess the effect of the intervention on the oncologist's level of patient
involvement, on patient satisfaction and coping and to explore the role of key persons
accompanying the patient.
The investigators expect that patients who have the opportunity to rehearse their
informative needs before the consultation will ask a greater number of questions which in
turn will determine their greater involvement by the physician and a greater number of
satisfied needs. The investigators expect also that the straightforward use of a list of
printed questions of potential relevance for cancer patients and their companions at an
early stage of illness, by modifying the process of information exchange, increases their
participation and satisfaction with the consultation, with potential benefits for treatment
adherence and consequently treatment efficacy.
n/a
Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Double Blind (Subject, Caregiver, Investigator, Outcomes Assessor), Primary Purpose: Supportive Care
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