To evaluate the current medical practice and its influence on health-related quality of life, in patients who are treated with injectable bone antiresorptive drugs (biphosphonates or denosumab) for at least one year.
This protocol will evaluate the pursuit of injectable bone antiresorptive treatments or their switch to oral biphosphonates, or treatment stop, in the contexte of medical practice. The primary end-point is the health-related quality of life (QoL). Secondary endpoints are safety, overall survial, the impact of toxicities of the treatment on QoL, and the description of supportive care.
Study Type
INTERVENTIONAL
Allocation
NA
Purpose
OTHER
Masking
NONE
Enrollment
148
Centre Hospitalier Régional Universitaire de Besançon
Besançon, France
Hôpital Nord Franche-Comté
Montbéliard, France
evaluation of 4 targeted dimensions of the EORTC-QLQ-BM22 quality of life questionarie
evaluation of 4 parameters: painful sites characteristics of pain, functional impairment, psychosocial aspect
Time frame: to 6 months
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