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NCT07412002 · Children's Oncology Group

Quality of End-of-Life Care for Children With Cancer

What this study is about

This study examines the role of access to care, patient/family interactions with the healthcare system, and stress in explaining variations in quality of end of life care. The data collected from this study may help researchers develop a model for identifying patients at risk of low quality end of life care as well as recommendations for potential future interventions.

View original scientific description

This study examines the role of access to care, patient/family interactions with the healthcare system, and stress in explaining variations in quality of end of life care. The data collected from this study may help researchers develop a model for identifying patients at risk of low quality end of life care as well as recommendations for potential future interventions.

Who can participate

This study lists these criteria on ClinicalTrials.gov. A study coordinator reviews eligibility during screening — this page does not determine whether you qualify.

Inclusion criteria

  • Index Child (COG Registered Patient):
  • Must be deceased
  • \< 18 years old at time of death
  • Diagnosed with any oncologic condition
  • History of enrollment on Stratum 1 of APEC14B1, Project:EveryChild
  • Note: history of treatment on a COG therapeutic trial is not required
  • Resided in the United States, including Puerto Rico, as evidenced by most recent address, at the time of death Bereaved Parent(s):
  • Must be a parent, legal guardian, or caregiver (biological or non-biological) of an eligible Index Child enrolled on APEC14B1 with current Consent to Future Contact (e.g., from the APEC14B1 Part B Consent)
  • Self-reported confirmation of familiarity with the care received by the Index Child in the last month of their life
  • Bereaved parent must understand English or Spanish (written and/or spoken)
  • Must be a parent/guardian/key contact from the Index Child's APEC14B1 Future Contact study record or must be referred by one of the APEC14B1 contacts
  • Bereaved parent must be \>= 18 years old at the time of ALTE24C1 study enrollment Regulatory Requirements:
  • Bereaved parent must provide verbal or implied informed consent
  • For all participants, all institutional, FDA, and NCI requirements for human studies must be met

Where

  • Wilmington, Delaware
  • Hollywood, Florida
  • Jacksonville, Florida
  • Orlando, Florida
  • Pensacola, Florida
  • Grand Rapids, Michigan
  • Kalamazoo, Michigan
  • Pittsburgh, Pennsylvania
  • Providence, Rhode Island
  • Dallas, Texas

Frequently asked questions

What is a clinical trial?

A clinical trial is a research study that tests new medical treatments, drugs, devices, or procedures to determine their safety and effectiveness. Trials are carefully designed and monitored to protect participants while advancing medical knowledge.

Is it safe to participate?

Clinical trials follow strict safety guidelines and ethical standards. Trials must be reviewed and approved, and participants are closely monitored by medical professionals throughout the study. You can withdraw at any time if you choose.

Will I be compensated?

Many clinical trials offer compensation for your time, travel expenses, and inconvenience. The specific compensation varies by study and will be discussed during the screening process. All study-related medical care is typically provided at no cost to participants.

Will I receive a placebo instead of treatment?

When effective treatment exists, participants typically receive either the standard treatment plus the study intervention, or the standard treatment plus placebo. You would not be denied effective care. Placebos are primarily used when no proven treatment is available, or in addition to standard care. Your trial consent form will clearly explain what treatments you may receive.

Can I leave a trial if I change my mind?

Absolutely. Participation in clinical trials is completely voluntary. You have the right to withdraw from the study at any time, for any reason, without penalty or loss of benefits to which you are otherwise entitled.

How long does a clinical trial last?

Trial duration varies widely depending on the study design and purpose. Some trials last just a few weeks, while others may continue for months or years. The study coordinator will provide specific timeline information during your screening call.

Data: ClinicalTrials.gov · synced Jul 6, 2026 · Source of record for eligibility and locations

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1 of 2425 participants interested
0% interest

See if this study fits

A short prescreen based on this study's listed criteria. A coordinator confirms eligibility — this is not a medical assessment.

Preparing your pre-screening questions…

Study locations

Choose your preferred location, or select flexible during enrollment.

RECRUITING

Wilmington

Delaware

Location available
RECRUITING

Hollywood

Florida

Location available
RECRUITING

Jacksonville

Florida

Location available
RECRUITING

Orlando

Florida

Location available
RECRUITING

Pensacola

Florida

Location available
RECRUITING

Grand Rapids

Michigan

Location available
RECRUITING

Kalamazoo

Michigan

Location available
RECRUITING

Pittsburgh

Pennsylvania

Location available
RECRUITING

Providence

Rhode Island

Location available

And 1 more location available.

Express your interest

Share your contact details and a study coordinator can follow up about screening.

Secure & Confidential

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

What participation can include

  • Study-related care provided by the research team
  • Close monitoring by medical professionals
  • Possible compensation for time and travel*
  • The option to withdraw at any time
  • Contributing to medical research that may help future patients

*Compensation varies by study. Confirm details with coordinator.

Typical next steps

  1. 1.Submit this form
  2. 2.Phone screening
  3. 3.In-person assessment if eligible
  4. 4.Begin participation

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Looking for Childhood Hematopoietic and Lymphatic System Neoplasm Treatment in Wilmington?

Join others in Delaware exploring innovative treatment options through clinical research

Childhood Hematopoietic and Lymphatic System Neoplasm Treatment Options in Wilmington, Delaware

If you're searching for Childhood Hematopoietic and Lymphatic System Neoplasm treatment in Wilmington, participating in a clinical research study may provide access to innovative approaches under expert medical supervision. This study is actively recruiting participants in Wilmington, Hollywood, Jacksonville and surrounding areas.

Clinical trials offer participants the opportunity to receive cutting-edge treatments while contributing to medical research that may help future patients with Childhood Hematopoietic and Lymphatic System Neoplasm. All study-related care is provided at no cost to participants.

Local Sites
3 locations in Delaware
Now Enrolling
Up to 2425 participants
Quick Start
Screening available now

Why Consider a Clinical Trial for Childhood Hematopoietic and Lymphatic System Neoplasm?

Potential Benefits

  • Access to new treatment approaches before public availability
  • Close monitoring by experienced medical professionals
  • Study-related care provided at no cost
  • Contribute to medical research for Childhood Hematopoietic and Lymphatic System Neoplasm

What to Expect

  • Initial screening to determine eligibility
  • Regular check-ups and monitoring visits
  • Possible compensation for time and travel
  • You can withdraw at any time

Frequently Asked Questions About This Childhood Hematopoietic and Lymphatic System Neoplasm Study

Important Clinical Trial Information

This information is provided for educational purposes and does not constitute medical advice. Clinical trial participation involves potential risks and benefits. Eligibility requirements apply and will be assessed during the screening process.

Study identifier: NCT07412002. For complete study details, visit ClinicalTrials.gov. Always consult with your healthcare provider before making decisions about your medical care or participating in clinical research.