Status:

NOT_YET_RECRUITING

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

Lead Sponsor:

M.D. Anderson Cancer Center

Conditions:

Family Centered

Black Ethnicity

Eligibility:

MALE

18+ years

Phase:

NA

Brief Summary

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,...

Detailed Description

Primary Objectives • Determine the extent to which MVPA and overall diet quality have improved in Black PCa survivors and their caregivers in the family-centered intervention group, compared to those...

Eligibility Criteria

Inclusion

  • 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.

Exclusion

    Key Trial Info

    Start Date :

    February 14 2026

    Trial Type :

    INTERVENTIONAL

    Allocation :

    ESTIMATED

    End Date :

    June 30 2033

    Estimated Enrollment :

    648 Patients enrolled

    Trial Details

    Trial ID

    NCT07164456

    Start Date

    February 14 2026

    End Date

    June 30 2033

    Last Update

    September 10 2025

    Active Locations (1)

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    Page 1 of 1 (1 locations)

    1

    MD Anderson Cancer Center

    Houston, Texas, United States, 77030