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NCT06674863Recruiting

Addressing Health Literacy With a Tailored Survivorship Care Plan

Addressing Health Literacy With a Tailored Survivorship Care Plan to Improve Access in Underserved African American Prostate Cancer Patients

Source: ClinicalTrials.gov · Last updated 30 Sept 2026

Brief summary (registry, in English)

This clinical trial compares the impact of a tailored survivorship care plan (SCP) to a standard SCP on the understanding of and access to survivorship care in black or African American patients with prostate cancer that has not spread to other parts of the body (localized) or that has spread from where it first started (primary site) to a limited number of places in the body (oligometastatic). SCPs summarize treatment history and recommendations for monitoring and maintaining health, and may also include potential long term effects of treatments received. The intention of a SCP is to help patients participate in their own health care. However, many patients have below basic levels of health literacy, meaning, they have a lower ability to obtain, communicate, process and understand basic health information and services to make health decisions. In fact, poor health literacy has been linked with worse quality of life in prostate cancer survivors. A tailored SCP includes the addition of an educational supplement based on lower reading and writing skills (low literacy) and may address health literacy barriers to understanding of treatment options and side effects. A standard SCP uses a template based on the American Society of Clinical Oncology (ASCO) guidelines for prostate cancer. A tailored SCP with low literacy educational supplements may be more effective compared to a standard SCP in improving understanding and access to survivorship care in black or African American patients with localized or oligometastatic prostate cancer.

Status (registry)
Recruiting
Study type
Interventional
Enrollment
150 (estimated)
First submitted
4 Nov 2024
Start date
7 Nov 2025
Primary completion date
31 Dec 2029
Lead sponsor
Emory University
NCT number
NCT06674863

What you commit to

  • Study type: Interventional
  • Planned participants: 150
  • From 7 Nov 2025 to the primary completion date, 31 Dec 2029
  • 3 sites in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Other illness

  • Dementia or cognitive impairment per provider clinical assessment
  • Recurrent prostate cancer after primary treatment
  • Diagnosis of active second malignancy requiring treatment

Age

  • Less than 18 years of age at the time of informed consent

Other

  • Unable to give informed consent in the judgement of the patient's oncology provider
  • Individuals who are not able to clearly understand English since the outcome measures require understanding of English

Who the study is looking for

  • Black and African American men who are disease-free after completing primary surgery and/or radiation treatment for localized or oligometastatic prostate cancer between 1 to 4 years prior to enrollment. (Race/ethnicity per medical records and self report)
  • Patients who are still receiving adjuvant androgen deprivation therapy following primary radiation with non-palliative intent may be included

Age in the registry: 18 years to - · Sex: Male · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (3)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Emory University Hospital/Winship Cancer Institute
Coordinator of this site? Confirm its status
AtlantaUnited StatesRecruiting
Atlanta VA Medical Center
Coordinator of this site? Confirm its status
AtlantaUnited StatesRecruiting
Grady Memorial Hospital
Coordinator of this site? Confirm its status
AtlantaUnited StatesRecruiting

This page is information, not medical advice. Discuss any trial with your doctor.