Mattoon, ILNCT07278739Now EnrollingIRB Ready

Malignant Solid Neoplasm Clinical Trial in Mattoon, IL

Access cutting-edge malignant solid neoplasm treatment through this clinical trial at a research site in Mattoon. Study-provided care at no cost to qualified participants.

Sponsored by SWOG Cancer Research Network

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Expert Care in Mattoon

Access malignant solid neoplasm specialists at no cost

IRB Approved

This study follows strict safety protocols and ethical guidelines

No-Cost Care

All study-related malignant solid neoplasm treatment provided free

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Check if you qualify for this malignant solid neoplasm clinical trial in Mattoon, IL

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Your information is protected and will only be shared with the research team.

Why Participate?

  • No-Cost Study Care

  • Local to Mattoon

    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 Mattoon site if eligible
  4. 4Begin participation

About This Malignant Solid Neoplasm Study in Mattoon

This clinical trial evaluates an educational program called Algorithm-Enabled Patients Activated in Cancer Care Through Teams (A-PACT) for reducing unplanned hospital visits and improving goals of care conversations with providers among patients with solid cancers. A-PACT is an educational program where lay health workers (educators) help patients talk with their health care team about issues that matter most to them (goals of care). During A-PACT sessions, patients receive assistance in formulating health care and end of life care preferences, assistance in completing advance directives, guidance on how to engage in these conversations with family members, friends, and clinical teams, and encouragement to discuss these topics with their clinical team. A-PACT may reduce unplanned hospital visits and improve goals of care communication with providers among patients with solid cancers.

Sponsor: SWOG Cancer Research Network

Who Can Participate

Inclusion Criteria

Participants must have a diagnosis of a solid tumor malignancy of any stage
Participants must be identified as high risk, defined as having 6 month mortality estimate from machine learning (ML) algorithm \>= 20%
Participants must not be receiving or have pre-existing plans to enter hospice care at the time of study registration
Participant must be actively receiving or planning to receive systemic anti-cancer therapy (defined as any oral, injection, or intravenous therapy against cancer) within 3 months after registration
NOTE: This includes chemotherapy (conventional or cytotoxic chemotherapy), hormone therapy, targeted therapy, and immunotherapy
NOTE: Participants are allowed to be co-enrolled on other clinical trials including trials using investigational agents
Participants must be \>= 18 years of age at the time of study enrollment
Participants who can complete Patient Reported Outcome (PRO) questionnaires in English or Spanish must be willing to 1) complete PROs at all scheduled assessments; and 2) complete the pre-registration (baseline) PRO forms within 14 days prior to registration
Participants must be able to provide a valid telephone number for the purpose of being contacted by the lay health worker
NOTE: As a part of the Oncology Patient Enrollment Network (OPEN) registration process the treating institution's identity is provided in order to ensure that the current (within 365 days) date of institutional review board approval for this study has been entered in the system
Patient and clinician participants must be informed of the investigational nature of this study and must sign and give informed consent in accordance with institutional and federal guidelines. This protocol does not permit use of Legally Authorized Representative NOTE: For this study, in the OPEN registration, clinician participants will be listed as their own treating investigator. However, clinician participants must not consent themselves or sign their own eligibility criteria forms

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 Mattoon?

Yes, this clinical trial (NCT07278739) has an active research site in Mattoon, 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.

Malignant Solid Neoplasm Treatment Options in Mattoon, IL

If you're searching for malignant solid neoplasm treatment options in Mattoon, IL, this clinical trial (NCT07278739) 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 Mattoon research site is actively enrolling participants for this clinical trial. You'll receive care from experienced malignant solid neoplasm 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.

Looking for more options? Browse all malignant solid neoplasm clinical trials near you to find additional studies recruiting in your area.

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