About this trial
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.
Eligibility criteria
This trial does not accept healthy volunteersQualifiers
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.
Disqualifiers
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.
Have serious medical conditions (e.g., cancer, congestive heart failure, stroke, and dementia)
Trial design
Single group
Treatments tested in this trial
Education sessions
Other interventionRemote and In person sessions
Questionnaire
Other interventionQuestionnaires given a 3,6,12 mouth follow ups
Treatment groups
Trial outcomes
Primary outcomes
Physical Activity Readiness Questionnaire
Sponsors and contacts
Click on the lead sponsor to view all of their trials.