Finding studies
Finding studies
Take this into the appointment.
Saves the questions and what to expect into your notes, next to the visit they belong to.
Karen Craver
CONTACT
Lead
Wake Forest University Health Sciences
With
PRIMARY OBJECTIVE: I. To compare change in research self-efficacy (RSE) scores from baseline to end of study (12 months post-randomization) between APPs in the COACH-APP intervention compared to the education control. SECONDARY OBJECTIVES: I. To compare National Cancer Institute (NCI) Community Oncology Research Program (NCORP) engagement post-study (12-months) for APPs in the COACH-APP intervention compared to the education control. II. To compare changes from baseline to post-study in APP ratings of research care team integration (Assessment for Collaborative Environments \[ACE\]-15) between the COACH-APP intervention and education control. III. To compare practice-level NCORP and National Clinical Trial Network (NCTN) study activity as measured by total number of accruals (patient, non-patient, and organizational) and number of actively recruiting NCORP and NCTN studies over 24 months between practices with APPs receiving the COACH-APP intervention versus those in education control. IV. Within the COACH-APP intervention group, to measure acceptability, feasibility, and appropriateness of the COACH-APP intervention for APPs and COACH-APP mentors to guide future implementation. V. Within the COACH-APP intervention group, conduct semi-structured interviews with a sub-set of mentors, APPs, and other key research team members (collaborating oncologists and clinical research professionals) to assess: * Va. Perceptions of feasibility, acceptability, and appropriateness of the COACH-APP intervention; * Vb. Potential effects of the COACH-APP intervention on the research care team functioning and environment; * Vc. Potential effects of the COACH-APP intervention on patient care quality and access to clinical trials; * Vd. Practice-level barriers and facilitators of APP engagement in research activities.
Age
18–any
Sex
ALL
Healthy volunteers
Accepted
