A program to improve cancer care for the community

Morehouse Total Cancer Care Protocol: A Lifetime Partnership With Patients Who Have or May be at Risk of Having Cancer

Observational Morehouse School of Medicine · NCT04804878

This study is trying to improve cancer care for African American patients by collecting health information and biological samples to help develop better treatments tailored to their needs.

Quick facts

Study typeObservational
Enrollment5000 (estimated)
Ages18 Years and up
SexAll
SponsorMorehouse School of Medicine Academic / other
Locations1 site (Atlanta, Georgia)
Trial IDNCT04804878 on ClinicalTrials.gov

What this trial studies

The Morehouse Total Cancer Care program aims to enhance cancer treatment standards by creating a centralized biorepository of biological samples and associated data from thousands of African American cancer patients and those at risk. This observational study will collect blood, tissue, and other biological samples, along with survey and medical records data, to facilitate biomarker discovery and personalized medicine approaches. Participants will provide informed consent to allow researchers to study their health information and biological materials over their lifetime. The initiative focuses on translating research findings into community oncology practices.

Who should consider this trial

Good fit: Ideal candidates include individuals aged 18 and older who have been diagnosed with cancer or are at risk of developing cancer.

Not a fit: Patients who are under 18 years old or do not have a cancer diagnosis or risk may not benefit from this program.

Why it matters

Potential benefit: If successful, this program could lead to improved cancer care and personalized treatment options for patients.

How similar studies have performed: Other studies have shown success in establishing biorepositories for cancer research, indicating that this approach is promising.

Eligibility criteria

Show full inclusion / exclusion criteria
Inclusion Criteria:

1. 18 years of age and older.
2. Diagnosed with cancer, or at risk for cancer. This includes anyone in the general population, but our primary focus will be on patients with a cancer diagnosis.
3. Able to understand and sign the TCCP Informed Consent and Research Authorization form directly or through an authorized representative. The Informed Consent and Research Authorization will be available in both English and Spanish languages

Exclusion Criteria:

None

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Where this trial is running

Atlanta, Georgia

Study contacts

How to participate

  1. Review the eligibility criteria above with your treating physician.
  2. Visit the official trial page on ClinicalTrials.gov for the most current contact information and recruitment status.
  3. Contact the listed study coordinator or principal investigator to request pre-screening. Pre-screening is free and never obligates you to enroll.
Conditions CancerCancer Risk
Last reviewed 2026-06-09 by the Find a Trial editorial team. Information on this page is for educational purposes and is not medical advice. Always consult qualified healthcare professionals about clinical trial participation.