FitBit and coaching aim to boost exercise in prostate cancer patients
NCT ID NCT05755490
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This pilot study tested a behavioral program called PROWESS for Black and Hispanic men with prostate cancer who are on hormone therapy (ADT). The program included video or in-person sessions with a psychologist or social worker and a FitBit to track activity. The goal was to see if the program could help men exercise more, reduce side effects, and improve quality of life. Only 14 people took part, so results are very preliminary.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- behavioral change intervention (PROWESS) with FitBit
- What this could lead to
- If successful, this could point toward a practical way to help prostate cancer patients on hormone therapy stay active and feel better.
- What could go wrong
- This is a very small pilot study with only 14 participants, so results may not apply to everyone. The program may not lead to lasting changes in exercise or quality of life.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Phase
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Not a phased trial
Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.
- Participants
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14 people
The number who actually took part.
- Started
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Aug 2023
- Finished
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Sep 2025
- Lead sponsor
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Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
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18 years and older
- Sex
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Male participants only
- Healthy volunteers
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Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: * Diagnosed with prostate cancer. * Planning to be on androgen deprivation therapy (ADT) for at least three months * Black Race AND/OR Hispanic/Latino Ethnicity (confirmed by patient self-report) * Verbal fluency in English or Spanish. * Receiving ongoing oncology care at MGH Cancer Center. * Age ≥ 18 years. * Self-Report less than or equal to 150 minutes of moderate or vigorous structured exercise per week, as assessed by the Exercise is Medicine Physical Activity Vital Sign Assessment * Completion of baseline assessment Exclusion Criteria: * Unwilling or unable to participate in the study. * Significant psychiatric, cognitive or other comorbid disease which the treating clinician believes prohibits informed consent or participation in the study. * Currently receiving chemotherapy. * Prognosis less than 6 months, per the judgment of the primary oncologist. * Medical contraindication to physical activity, as assessed by outpatient oncologist.
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
Contacts and locations
Locations
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Massachusetts General Hospital Cancer Center
Boston, Massachusetts, 02215, United States
More trials for these conditions
Other studies related to the condition(s) this trial covers.
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