Galesburg, ILNCT06904391Now EnrollingIRB Ready

Other Clinical Trial in Galesburg, IL

Access cutting-edge other treatment through this clinical trial at a research site in Galesburg. Study-provided care at no cost to qualified participants.

Sponsored by Wake Forest University Health Sciences

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Expert Care in Galesburg

Access other specialists at no cost

IRB Approved

This study follows strict safety protocols and ethical guidelines

No-Cost Care

All study-related other treatment provided free

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Check if you qualify for this other clinical trial in Galesburg, IL

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Why Participate?

  • No-Cost Study Care

  • Local to Galesburg

    Convenient for IL residents

  • Cutting-Edge Treatment

    Access to innovative therapies

  • Expert Medical Care

    Close monitoring by specialists

  • Possible Compensation*

    For time and travel

*Compensation varies by study. Confirm details with coordinator.

Simple Process

  1. 1Submit this form
  2. 2Phone screening
  3. 3Visit Galesburg site if eligible
  4. 4Begin participation

About This Other Study in Galesburg

This clinical trial evaluates whether a mentorship and education intervention called COACH-APP works to improve advanced practice providers' (APPs) confidence in their ability to participate in clinical research (research self-efficacy). APPs are skilled clinicians who are routinely part of cancer care teams, but who may not routinely be part of the research care team at community oncology sites. The COACH-APP program provides focused education and structured mentorship to assist in meaningful integration to the research care team, which may increase research self-efficacy among APPs and ultimately improve patient care and access to clinical trials.

Sponsor: Wake Forest University Health Sciences

Who Can Participate

Inclusion Criteria

APP PRACTICE: Must have one practicing APP who can dedicate approximately 2 hours/month to participate in the intervention and study activities over a 12-month period, supported by their direct supervisor via the APP Support Statement
APP PRACTICE: Must attest to research infrastructure that can support APP trial enrollment, as declared on the APP Practice Attestation
APP PRACTICE: Must have submitted the APP Practice Attestation within the Study Interest Survey
APP PRACTICE: Must have received the required APP practice ID for Oncology Patient Enrollment Network (OPEN) enrollment in the Study Selection Email prior to enrollment
APP PRACTICE: Must enroll eligible practice site(s) in OPEN within 14 days of receiving the Study Selection Email.
APP: Practicing nurse practitioner (NP) or physician assistant (PA) registered as an active non-physician investigators (NPIVR) within the National Cancer Institute (NCI) Registration and Credential Repository (RCR)
APP: Treats oncology patients at practice that is actively recruiting to NCORP and/or NCTN trials
APP: Not planning to leave their clinical position within the APP practice (defined as one or more NCORP affiliate or sub-affiliate site\[s\] where the APP participating in the study sees patients and clinical research activities occur) in the next 12 months at enrollment
APP: Willing to participate in a 30-minute recorded phone interview, if selected
APP: Completed and submitted the APP Attestation within the Study Interest Survey
APP: Completed and submitted an APP Support Statement from their direct supervisor approving participation in this study, within the Study Interest Survey
APP: Identify and obtain signed Research Care (RC) Team Acknowledgements from two members (defined below) of their research care team to assist them in this study. The RC team for this study will consist of an oncologist and clinical research professional (i.e., clinical research coordinator, clinical research associate clinical research nurse, etc.) that the APP collaborated with over the past 6 months or could collaborate with in the future to enroll patients on NCORP and/or NCTN trials
APP: Must have received the required APP practice ID for OPEN enrollment in the Study Selection Email
APP: Must enroll consented APPs in OPEN within 14 days of receiving the Study Selection Email
MENTOR: Must be a practicing APP chosen by the WF-2403 COACH-APP Study MPIs
MENTOR: Must have the following criteria:
Clinical practice experience in a practice that enrolls to NCORP and/or NCTN trials.
Participation in a leadership role within NCTN or NCORP (i.e., serving on a Research Base committee, working group, taskforce or as a site PI)
Willing to complete COACH-APP mentor training.
Willing to complete a 30-minute recorded phone interview about their experience with the COACH-APP intervention
RESEARCH CARE TEAM INTERVIEW: Must be an identified member of the Research Care Team for an APP assigned to the COACH-APP intervention arm. The Research Care Team will be reviewed by the APP in the 12 month survey for any changes
RESEARCH CARE TEAM INTERVIEW: Willing to participate in a recorded phone interview (approximately 30 minutes) to assess their perceptions of the COACH-APP intervention, including feasibility, acceptability, and impact

Exclusion Criteria

APP PRACTICE: APP practice has an APP serving as a COACH-APP intervention mentor
APP PRACTICE: Another APP at the same APP practice is already enrolled in this study (i.e., only 1 APP is allowed per APP practice)
APP PRACTICE: Affiliate/sub-affiliate site(s) within this APP practice are already enrolled or are intended to be enrolled in this study under another APP practice
APP: Has already completed the SWOG APP workshop
APP: Served as a site principal investigator (PI) for an NCORP or NCTN study at any time
APP: Participated as a presenter for the SWOG APP workshop
APP: Participated on the planning committee for The Advanced Practice Provider Clinical Trials Research Manual
APP: Participated on the planning committee for the SWOG APP workshop
APP: Past or current member of SWOG APP Task Force Committee
APP: Past or current member of Eastern Cooperative Oncology Group- American College of Radiology Imaging Network (ECOG-ACRIN) APP Committee
MENTOR: Must not work at NC002-Wake Forest University Health Sciences or its affiliate/subaffiliate sites

Not sure if you qualify? Submit your interest and a study coordinator will help determine your eligibility.

Frequently Asked Questions

Q:Is this study available in Galesburg?

Yes, this clinical trial (NCT06904391) has an active research site in Galesburg, IL that is currently enrolling participants.

Q:Is it safe to participate?

Clinical trials follow strict safety guidelines and ethical standards. This study has been reviewed and approved, and participants are closely monitored by medical professionals. You can withdraw at any time.

Q:Will I be compensated?

Many clinical trials offer compensation for your time and travel expenses. Specific compensation details will be discussed during the screening process. All study-related medical care is provided at no cost.

Q:Can I leave the trial if I change my mind?

Absolutely. Participation is completely voluntary. You have the right to withdraw from the study at any time, for any reason, without penalty.

Still have questions? Our study coordinators are here to help.

Other Treatment Options in Galesburg, IL

If you're searching for other treatment options in Galesburg, IL, this clinical trial (NCT06904391) may be an excellent opportunity. Clinical trials provide access to cutting-edge treatments that aren't yet available to the general public, often at no cost to participants.

Our Galesburg research site is actively enrolling participants for this clinical trial. You'll receive care from experienced other specialists who are at the forefront of medical research. All study-related care, including examinations, treatments, and monitoring, is provided at no cost to qualified participants.

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