Not provided
| ID | Type | Description | Link |
|---|---|---|---|
| NCI-2025-06570 | Other Identifier | NCI-CTRP Clinical Registry |
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
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.
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
Not provided
Not provided
Not provided
Not provided
Not provided
| Label | Type | Description | Intervention Names |
|---|---|---|---|
| Family-centered intervention | Experimental | Includes a nutrition education session, a PA education session, and 12 health-coaching calls, all conducted via Zoom or phone. |
|
| survivor-only intervention | Experimental | Includes a nutrition education session, a PA education session, and 12 health-coaching calls, all conducted via Zoom or phone. |
|
| Health education control | Experimental | Will focus on enhancing participants' intrinsic motivation and problem-solving skills related to improving diet quality and engaging in PA. A total of 12 sessions will be provided, with approximately 2 sessions per month |
|
| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| Education sessions | Other | Remote and In person sessions |
|
| Measure | Description | Time Frame |
|---|---|---|
| Physical Activity Readiness Questionnaire | Through study completion; an average of 1 year |
Not provided
Not provided
Eligibility Criteria
Survivors are eligible if they
Caregivers are eligible if they:
Exclusion Criteria
Survivors are excluded if they:
Caregivers are excluded if they:
males
Not provided
Not provided
Not provided
| Name | Role | Phone | Extension | |
|---|---|---|---|---|
| Dalnim Cho, MD | Contact | 713-745-8476 | dcho1@mdanderson.org |
| Name | Affiliation | Role |
|---|---|---|
| Dalnim Cho, MD | MD Andersson Cancer Center | Principal Investigator |
| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| MD Anderson Cancer Center | Recruiting | Houston | Texas | 77030 | United States |
Not provided
| Label | URL |
|---|---|
| MD Anderson Cancer Center | View source |
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
| Questionnaire | Other | Questionnaires given a 3,6,12 mouth follow ups |
|
| ID | Term |
|---|---|
| D011795 | Surveys and Questionnaires |
| ID | Term |
|---|---|
| D003625 | Data Collection |
| D004812 | Epidemiologic Methods |
| D008919 | Investigative Techniques |
| D017531 | Health Care Evaluation Mechanisms |
| D011787 | Quality of Health Care |
| D017530 | Health Care Quality, Access, and Evaluation |
| D011634 | Public Health |
| D004778 | Environment and Public Health |
Not provided
Not provided