Ignite Creation Date:
2024-10-26 @ 3:43 PM
Last Modification Date:
2024-10-26 @ 3:43 PM
Study NCT ID:
NCT06648278
Status:
RECRUITING
Last Update Posted:
None
First Post:
2024-10-16
Brief Title:
Patient Care Outreach Navigation Technology and Support 20
Sponsor:
None
Organization:
None
Study Overview
Official Title:
The Patient Care Outreach Navigation Technology and Support 20 Study
Status:
RECRUITING
Status Verified Date:
2024-10
Last Known Status:
None
Delayed Posting:
No
If Stopped, Why?:
Not Stopped
Has Expanded Access:
No
If Expanded Access, NCT#:
N/A
Has Expanded Access, NCT# Status:
N/A
Acronym:
COUNTS2
Brief Summary:
This is a feasibility study employing virtual patient navigation for underserved individuals who speak English Chinese or Spanish and were diagnosed with breast cancer to determine the extent of usability for a virtual patient navigation portal serving people in underserved communities While not able to entirely replace in-person interactions virtual patient navigation may be used to expand reach and availability of navigation services to a much greater segment of the population
Detailed Description:
Patient COUNTS 20 aims to improve and scale up the current Patient COUNTS program
PRIMARY OBJECTIVES
I Identify underserved individuals who speak English Chinese or Spanish and were diagnosed with breast cancer through collaboration with Zuckerberg San Francisco General Hospital ZSFG University of California San Francisco clinics Athena University of California San Francisco registries via medical chart review and community organization collaborators
II Conduct outreach to potential participants to let them know about the availability of virtual patient navigation via the Patient Care Outreach Navigation Technology and Support COUNTS web portal and the Patient COUNTS patient navigation program NCT03867916
III Provide patient navigation virtually
OUTLINE
The patient COUNTS portal will be available in English and expanded to include content in Chinese and Spanish An initial cohort of focus group of 20 participants 15 breast cancer patients 5 navigators social workers caregivers or other person involved in breast cancer care will help develop the culturally and language specific components of the COUNTS program Following implementation 100 breast cancer patients will participate in an online patient navigation program and 40 family members of breast cancer patients will be enrolled Participants will use the online COUNTS portal to access navigation program and may choose to have onlinevirtual navigation support or in-person navigation support Participants also complete data collection and surveys over 15 minutes via web portal at baseline and 6 months and user experience survey at end of program participation
PRIMARY OBJECTIVES
I Identify underserved individuals who speak English Chinese or Spanish and were diagnosed with breast cancer through collaboration with Zuckerberg San Francisco General Hospital ZSFG University of California San Francisco clinics Athena University of California San Francisco registries via medical chart review and community organization collaborators
II Conduct outreach to potential participants to let them know about the availability of virtual patient navigation via the Patient Care Outreach Navigation Technology and Support COUNTS web portal and the Patient COUNTS patient navigation program NCT03867916
III Provide patient navigation virtually
OUTLINE
The patient COUNTS portal will be available in English and expanded to include content in Chinese and Spanish An initial cohort of focus group of 20 participants 15 breast cancer patients 5 navigators social workers caregivers or other person involved in breast cancer care will help develop the culturally and language specific components of the COUNTS program Following implementation 100 breast cancer patients will participate in an online patient navigation program and 40 family members of breast cancer patients will be enrolled Participants will use the online COUNTS portal to access navigation program and may choose to have onlinevirtual navigation support or in-person navigation support Participants also complete data collection and surveys over 15 minutes via web portal at baseline and 6 months and user experience survey at end of program participation
Study Oversight
Has Oversight DMC:
None
Is a FDA Regulated Drug?:
None
Is a FDA Regulated Device?:
None
Is an Unapproved Device?:
None
Is a PPSD?:
None
Is a US Export?:
None
Is an FDA AA801 Violation?:
None