ClinicalTrials.Veeva

Menu

Dietary Factors and Racial Disparities in Prostate Cancer Aggressiveness (PCaP)

University of South Carolina logo

University of South Carolina

Status

Completed

Conditions

Prostatic Neoplasm

Study type

Observational

Funder types

Other
Other U.S. Federal agency

Identifiers

NCT03289130
DAMD-11-1-0568

Details and patient eligibility

About

The North Carolina-Louisiana Prostate Cancer Project is a population-based case-only study of over 2,000 men newly diagnosed with prostate cancer designed to address racial differences in prostate cancer aggressiveness and survival through a comprehensive evaluation of social, individual, and tumor level influences on prostate cancer aggressiveness. Project 3 specifically aims to examine nutritional modulation of prostate cancer aggressiveness using dietary assessment and biomarker-based data on dietary factors.

Full description

A total of 2,258 (1,130 African Americans and 1128 European Americans) men newly diagnosed with prostate cancer in North Carolina and Louisiana were enrolled into the study between 2004 and 2009. Participants signed informed consent and were interviewed by a trained nurse who collected information on demographics, occupation, family history, health status, health care, prostate cancer diagnosis and screening history, medication use, anthropometrics, lifestyle factors (e.g., physical activity, smoking), and diet and supplement use. Research subjects were asked to recall their diet in the year prior to prostate cancer diagnosis via a modified version of the National Cancer Institute Diet History Questionnaire. Vitamin and supplement use in the year prior to prostate cancer diagnosis was assessed via a validated questionnaire, and current use was assessed by bottle label inventory. Blood, urine, and adipose tissue samples were collected.

Enrollment

2,258 patients

Sex

Male

Ages

40 to 79 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • first diagnosis of histologically confirmed adenocarcinoma of the prostate
  • 40-79 years old at diagnosis,
  • can complete the study interview in English,
  • do not live in an institution (nursing home),
  • are not cognitively impaired or in a severely debilitated physical state,
  • are not under the influence of alcohol, severely medicated, or apparently psychotic at the time of the interview.
  • must self-identify as at least part African American/Black or Caucasian American/White/European American.

Exclusion criteria

Trial contacts and locations

0

Loading...

Data sourced from clinicaltrials.gov

Clinical trials

Find clinical trialsTrials by location
© Copyright 2026 Veeva Systems