Stronger together: family lifestyle program aims to boost health in black prostate cancer survivors
NCT ID NCT07164456
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This study tests whether a family-centered program can help Black prostate cancer survivors and their caregivers eat better, be more active, and feel better overall. About 648 survivor-caregiver pairs will join, with some receiving the family program, some the survivor-only program, and some standard advice. The goal is to see if involving the whole family leads to healthier habits and improved quality of life.
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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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About 648 people
The number the study aims to enrol. It can still change while the study runs.
- Started
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Jan 2026
- Expected to finish
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Jun 2033
An estimate. End dates often move.
- 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.
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Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Eligibility Criteria Survivors are eligible if they * Are adults (≥18 years old) * Self-identify as Black or African American; * Were diagnosed with stage 0-III PCa; completed PCa treatment; (5) are able to be physically active, as determined by responses to the Physical Activity Readiness Questionnaire (PAR-Q); and * Have a family caregiver willing to participate together. Individuals under active surveillance for PCa will be included. Caregivers are eligible if they: * Are adults (≥18 years old) * Are able to be physically active, as determined by responses to the Exclusion Criteria Survivors are excluded if they: * Have a prior history of other cancer or have metastatic cancer. * Have planned concomitant immunotherapy, hormonal therapy, chemotherapy, or radiation therapy during the study period. * Meet physical activity recommendations (i.e., 150 min of moderate intensity physical activity per week); and (4) are currently participating in a lifestyle or weight management program. Caregivers are excluded if they: * Have serious medical conditions (e.g., cancer, congestive heart failure, stroke, and dementia) * Are currently participating in a lifestyle or weight management program.
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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.
How to take part
Only the study team decides who joins. These are the ways to reach them.
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The places running it
1 site. The list below names each one and where it is.
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The official record
ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.
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A doctor treating you
A doctor who knows your case can contact a study site on your behalf, and can tell you whether this study is worth pursuing at all.
Contacts and locations
Locations
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MD Anderson Cancer Center
RECRUITINGHouston, Texas, 77030, United States
More trials for these conditions
Other studies related to the condition(s) this trial covers.
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- New PET tracer targets ACP3 to spot prostate cancer
- Can a One-Week radiation course match four weeks for prostate cancer?
- Can a new PET tracer spot hidden prostate cancer spread?
- Can a gel cushion shield the rectum during prostate radiation?
- A scanner in the operating room could show surgeons exactly where prostate cancer remains