Actively Recruiting

Phase Not Applicable
Age: 18Years +
MALE
NCT07164456

Together Stronger: A Family-centered Lifestyle Intervention for Black Prostate Cancer Survivors and Their Caregivers

Led by M.D. Anderson Cancer Center · Updated on 2026-03-09

648

Participants Needed

1

Research Sites

389 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

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.

CONDITIONS

Official Title

Together Stronger: A Family-centered Lifestyle Intervention for Black Prostate Cancer Survivors and Their Caregivers

Who Can Participate

Age: 18Years +
MALE

Eligibility Criteria

Eligible

You may qualify if you...

  • Adults 18 years or older
  • Self-identify as Black or African American
  • Diagnosed with stage 0-III prostate cancer and completed prostate cancer treatment
  • Able to be physically active as determined by the Physical Activity Readiness Questionnaire
  • Have a family caregiver willing to participate together
  • Individuals under active surveillance for prostate cancer are included
Not Eligible

You will not qualify if you...

  • History of other cancers or metastatic cancer
  • Planned immunotherapy, hormonal therapy, chemotherapy, or radiation therapy during the study
  • Meet physical activity recommendations of 150 minutes per week of moderate intensity
  • Currently participating in a lifestyle or weight management program
  • Caregivers with serious medical conditions such as cancer, congestive heart failure, stroke, or dementia
  • Caregivers currently participating in a lifestyle or weight management program

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

MD Anderson Cancer Center

Houston, Texas, United States, 77030

Actively Recruiting

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Research Team

D

Dalnim Cho, MD

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

RANDOMIZED

Model

SINGLE_GROUP

Primary Purpose

SUPPORTIVE_CARE

Number of Arms

3

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