Summarizing ExperieNces with Site Enrollment in NCORP Cancer Care Delivery Research Studies
NCORP SENSE Project
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NCORP SENSE Project - Rationale
•Robust cancer care delivery research (CCDR) portfolio
•19 CCDR studies approved
•~2/3 assessing clinician and/or organizational characteristics
•10 cluster RCTs
•Challenges
•Delays in activating studies
•Compliance with protocol efficiency guidelines
•Site representativeness of participating sites
•The Need
•Understand effective strategies used by NCORP Research Bases to increase site enrollment on CCDR studies
Qualitative Assessment with NCORP Research Base Staff
Purpose:
Obtain feedback on effective strategies used by NCORP RBs regarding RB site enrollment experiences to cancer care delivery research (CCDR) studies
Identify best practices/lessons learned to expedite time to study activation and enhance site representativeness
Method:
Select one CCDR protocol for each Research Base (see Table 1)
For each protocol, conduct interviews (30-45 min) with key staff involved in study development, implementation, and coordination/ operations (n=28-35)
Key staff are CCDR Subcommittee Chairs/Co-Chairs, Study Chairs/Investigators, Study Coordinators, Operations Leads, and others as appropriate
Table 1. | |
Research Base | CCDR Protocol |
Alliance | A231601CD: Improving Surgical Care and Outcomes in Older Cancer Patients Through Implementation of an Efficient Pre-Surgical Toolkit (OPTI-Surg) |
NRG | NRG-CC007CD: Optimizing Survivorship Care Plans for Prostate Cancer Survivors who Receive Androgen Deprivation Therapy |
ECOG-ACRIN | EAQ171CD Smokefree – Implementing Virtual Tobacco Treatment in Community Oncology Practices (Smoke Free 2.0) |
COG | ACCL16N1CD: Documentation and Delivery of Guideline-Consistent Treatment in AYA Acute Lymphoblastic Leukemia |
SWOG | A Pragmatic Trial to Evaluate a Guideline Based Colony Stimulating Factor Standing Order Intervention and to Determine the Effectiveness of Colony Stimulating Factor Use as Prophylaxis for Patients Receiving Chemotherapy with Intermediate Risk for Febrile Neutropenia Trial Assessing CSF Prescribing Effectiveness and Risk (TrACER) |
URCC | URCC-18004CD: Understanding the Impact of Drug Shortages on Oncology Care Delivery |
Wake Forest | WF20817CD: Implementation of Smoking Cessation Services within NCORP Community Sites with Organized Lung Cancer Screening Programs (OaSiS) |
Delete red, none for SWOG
TRACER as pilot
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Next Steps
Email from Westat, Inc to schedule interviews
Directly to Research Base PIs and Study Co-Chairs
From: Melanie Chansky or Sophia Tsakraklides
NCI Lead
Brenda Adjei ([email protected]) with any questions or concerns
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