About this trial
The purpose of this research is to determine whether a 16-week culturally tailored, technology-based, aerobic and resistance exercise intervention improves cardiovascular risk factors in Black men diagnosed with prostate cancer and are undergoing androgen deprivation therapy (ADT), and whether it will also improve physical fitness and function, body composition, and outcomes such as quality of life, cancer symptoms, and self-esteem.
Participants in this study will be randomly assigned to one of two groups: 1) Aerobic and resistance exercise, or 2) Usual care.
Eligibility criteria
Qualifiers
Patients must meet all criteria to be eligible, including travel to Dana-Farber Cancer Institute (DFCI) to collect research data to address the study question.
Over 18 years old; children under the age of 18 will be excluded due to the rarity of the disease
Histologically diagnosed of localized or metastatic prostate cancer
Have been receiving androgen deprivation therapy (ADT) (i.e., luteinizing hormone-releasing hormone [LHRH] agonist/antagonist and/or androgen receptor [AR] agonist/antagonist) for at least one month with a plan to continue ADT for at least 4 months at the time of recruitment
Disqualifiers
Are not receiving ADT (i.e., LHRH agonist/antagonist and/or AR agonist/antagonist)
Pre-existing medical conditions such as uncontrolled cardiopulmonary disease, or metabolic diseases that could exacerbate with exercise
Are not English or Spanish speaking
Patients with secondary diagnosis (with the exception of basal cell carcinoma)
Trial design
Treatments tested in this trial
- Aerobic and resistance exercise
- Usual Care