NCT07164456Recruiting
Together Stronger: A Family-centered Lifestyle Intervention for Black Prostate Cancer Survivors and Their Caregivers
Source: ClinicalTrials.gov · Last updated 9 Mar 2026
Brief summary (registry, in English)
To establish the efficacy of the family-centered intervention in improving healthy lifestyle behaviors (MVPA and overall diet quality), as well as physical functioning, QoL, and family health climate, compared to survivor-only and control groups.
- Status (registry)
- Recruiting
- Study type
- Interventional
- Enrollment
- 648 (estimated)
- First submitted
- 4 Sept 2025
- Start date
- 13 Jan 2026
- Primary completion date
- 30 Jun 2031
- Lead sponsor
- M.D. Anderson Cancer Center
- Diseases
- Prostate cancer
- NCT number
- NCT07164456
What you commit to
- Study type: Interventional
- Planned participants: 648
- From 13 Jan 2026 to the primary completion date, 30 Jun 2031
- 1 site in 1 country
- Visits and tests: ask the trial team, the registry does not list them
Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.
Who cannot take part
Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.
Prior treatment
- Have planned concomitant immunotherapy, hormonal therapy, chemotherapy, or radiation therapy during the study period.
Other illness
- Have a prior history of other cancer or have metastatic cancer.
- Have serious medical conditions (e.g., cancer, congestive heart failure, stroke, and dementia)
Other
- Survivors are excluded if they:
- 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:
- Are currently participating in a lifestyle or weight management program.
Criteria the registry did not label
- 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
Age in the registry: 18 years to - · Sex: Male · Does not accept healthy volunteers
Sites (1)
Sites in registry order. Pick your city on the disease page to sort them by distance.
| Site | City | Country | Site status |
|---|---|---|---|
| MD Anderson Cancer Center Coordinator of this site? Confirm its status | Houston | United States | Recruiting |
This page is information, not medical advice. Discuss any trial with your doctor.