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Clinical Trial Summary

The goal of this research study is to conduct an open pilot of a behavioral change intervention called PROstate Cancer Wearables, Exercise, and Structured Supports (PROWESS) for integrating health behavior change tools and to increase exercise, reduce side effects of androgen deprivation therapy (ADT), and improve quality of life in Black and Hispanic/Latino men with prostate cancer. The name of the intervention used in this research study is: PROWESS (behavioral change intervention)


Clinical Trial Description

This research study is to test a behavioral change intervention called PROstate Cancer Wearables, Exercise, and Structured Supports (PROWESS) for integrating health behavior change tools with wearable technology, to increase exercise, reduce side effects of androgen deprivation therapy (ADT), and improve quality of life in Black and Hispanic/Latino men with prostate cancer on androgen deprivation therapy (ADT). Study procedures include screening for eligibility, intervention sessions, questionnaires and surveys, and an exit interview with study staff. Participation in this research study is expected to last for up to four months. The goal and primary outcome of this open pilot study is refinement of the intervention and study procedures to allow for us to conduct a larger feasibility study in the future. It is expected that about 10 people will take part in this research study. This research study is being supported by the MGH Cancer Center ;


Study Design


Related Conditions & MeSH terms


NCT number NCT05755490
Study type Interventional
Source Massachusetts General Hospital
Contact Daniel Lage, MD
Phone 617-726-5130
Email dlage@partners.org
Status Not yet recruiting
Phase N/A
Start date March 2023
Completion date December 31, 2023

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