Geriatric Assessment and Technology Evaluation in Prostate Cancer, ProsGATE Trial

Inclusion Criteria

• * Patients must have histologically or cytologically confirmed adenocarcinoma of prostatic origin without neuroendocrine differentiation or signet ring or small-cell histologic features * Patients must be metastatic by having at least one metastatic lesion seen at the time of diagnosis or upon initiation of treatment on bone scan or computed tomography (CT) or magnetic resonance imaging (MRI), or by next-generation molecular imaging (FDG, F-18 NaF, C-11 choline, F-18 fluciclovine, Ga-68 PSMA-11 PET/CT or MRI) * Age ≥ 65 years. Given the aforementioned GA tools are only validated in those aged 65 and older * Planned initiation of intensified hormone deprivation (ADT and ARSI) * Ability to understand and the willingness to sign a written informed consent document

Exclusion Criteria

• * Participants with previous exposure to ADT/ARSI within 12 months of diagnosis, except those who initiated ADT/ARSI within 12 weeks of enrollment * Participants who had surgical orchiectomy outside of 12 weeks before their metastatic diagnosis * Participants who have had previous chemotherapy for metastatic prostate cancer * Uncontrolled intercurrent illness * Participants with small-cell carcinoma of the prostate or brain metastasis * Participants who are not fluent in reading/writing English or Spanish * Biologic and Pregnant women are excluded from this study because prostate cancer is a disease of biological males * Participants with implantable cardiac devices * Participants with limb defects precluding smart-watch wear