Understanding and Enhancing Health-Related Social Needs (HRSN) Screening Among Community Oncology… (NCT06412029) | Clinical Trial Compass
By InvitationNot Applicable
Understanding and Enhancing Health-Related Social Needs (HRSN) Screening Among Community Oncology Practices
United States144 participantsStarted 2024-11-20
Plain-language summary
This study evaluates health related social needs screening processes in community oncology clinics.
Who can participate
Age range18 Years
SexALL
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Inclusion Criteria:
Part 1
NCORP PRACTICES:
* Must be an affiliate or sub-affiliate of an NCORP Community or Minority Underserved Community site
* Must provide outpatient oncology care
* Must be a NCORP practice (defined as one or more NCORP affiliates/sub-affiliates, that have a common administrative structure and share providers and/or patients)
* Must have identified two or more Practice Staff that are available and willing to participate on the Practice Interest Form
* Must have identified at least 1-3 outpatient oncology clinics willing to participate on the Practice Interest Form
CLINICS:
* 1-3 clinics within the practice should be selected
* Clinics may or may not be located in different physical locations
* The investigators will encourage NCORP practices to select clinics within a practice that differ in current or potential implementation of health related social needs (HRSN) screening (e.g., different clinic workflow or staff, different screening triggers, different tools), so that heterogeneity within NCORP practices can be captured
* Clinics must be willing to allow Practice Staff participants to observe the clinical operations in-person
PRACTICE STAFF:
* Must be willing and able to take time to observe in person and document 1-3 selected clinics within the practice (approximately 2-3 hours per clinic)
* Must be staff at the selected and enrolled practice. Suggestions of appropriate staff are cancer care delivery research (CCDR) Lead, research nurse, clini…
What they're measuring
1
HRSN screening reach (Part 1)
Timeframe: From study enrollment to approximately 4 and 16 weeks post initial study training
2
Barriers and facilitators influencing HRSN screening implementation
Timeframe: From study enrollment to time completion of key informant interviews, approximately within 6 months
3
Generation of a tailored implementation plan for each participating clinic
Timeframe: Between time of clinic selection and co-design workshop completion, to be no more than 6 months