Evaluation of Improvements in Patient-reported Quality of Life
Recruiting
N/A
Interventional Study
Breast Cancer
Quality of Life
Physical Activity
Sleep Quality
Stress
Pain
No Placebo Group
Every participant receives an active treatment — no one gets a placebo.
At a Glance
- Age
- 18 – 75
- Sex
- Female
- Study type
- Interventional
- Purpose
- Supportive Care
- Participants needed
- 110 (estimated)
- Sponsor
- Fundación para la Investigación del Hospital Clínico de Valencia · Other
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About This Trial
Local intervention trial for the evaluation of improvements in patient-reported Quality of Life and treatment satisfaction, in breast cancer patients (BCP), as a result of flexible treatment planning supported by REBECCA-collected real-world data, in comparison with standard care
Trial Locations
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Eligibility Criteria
Inclusion Criteria:
* Before patient registration, written informed consent must be given according to national and local regulations.
* Participants have had histologically proven stage I-III breast cancer undergoing endocrine treatment (with or without prior chemotherapy) no more than 12 months p…
Contacts
No contact information available.