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NCT Number: NCT07164456

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

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.

Recruiting

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Key information

Age range

18 year and older

Sex eligibility

Male

Study type

Interventional

Phase

Not applicable

Primary location

MD Anderson Cancer Center

Houston, Texas, 77030, United States

Location status: Recruiting

Location contact

Dalnim Cho, MD

CONTACT

[email protected]

713-745-8476

Dalnim Cho, MD

PRINCIPAL_INVESTIGATOR

About this study

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 in the survivor-only and control groups at post-intervention.

Secondary Objectives

  • Determine the extent to which, compared to those in the survivor-only and control groups, both survivors and caregivers in the family-centered group maintain the MVPA and high diet quality at the 6-month follow-up, and experience improved 6MWT, QoL, and family health climate at both post-intervention and 6-month follow-up.
  • Identify mediators and moderators of the family-centered intervention.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

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.

Treatment and study plan

Education sessions

Other

Remote and In person sessions

Questionnaire

Other

Questionnaires given a 3,6,12 mouth follow ups

Primary outcomes

  1. Physical Activity Readiness Questionnaire

    Time frame: Through study completion; an average of 1 year

Study contacts

Contact information is provided by the study sponsor or research team.

Dalnim Cho, MD

CONTACT

[email protected]

713-745-8476

Sponsors and collaborators

Lead sponsor

M.D. Anderson Cancer Center

Other

Registry information

Important dates

Study start
2026
Primary completion
2031
Study completion
2033
First posted
Sep 10, 2025
Registry last updated
Mar 9, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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