CompletedNot applicableNCT00453661
Official study title

Cancer Prevention and Treatment Demonstration for Ethnic and Racial Minorities

Study summary

The goal of this behavioral research study is to improve the use of cancer prevention services, increase early detection, and treatment of cancer. A secondary outcome of this demonstration project proposes that a structured patient navigator (PN) will reduce the cost of Medicare services.

Ask AI to explain this study
Start here

Key things to know

Main goalNot specified

This describes the study’s primary purpose.

What is being studiedQuestionnaire and Patient Navigator (PN)

The study team can explain what participation involves.

Who it may be forBreast Cancer · Cervical Cancer

These are broad labels—not an eligibility decision.

Checked against the public recordLast updated Oct 29, 2020 · Source: ClinicalTrials.gov

Is enrollment open?Completed

Ask the study team to confirm whether enrollment is open.

What kind of study?Not applicable

Observational

Where is it offered?1 U.S. location

Locations may change over time.

Who runs it?M.D. Anderson Cancer Center

Study sponsor

01
Study overview

What this study is about

Purpose
Not specified
Study type
Observational
Phase
Not applicable
Sponsor
M.D. Anderson Cancer Center
Interventions being studied
Behavioral: Questionnaire; Behavioral: Patient Navigator (PN)
02
Explore related studies

How this study is categorized

These labels come from structured fields and exact terms in the public record.

03
Public criteria

Who may be able to participate

The sponsor separates these requirements into two groups. You do not need to interpret them alone—use them to guide a conversation with the study team.

Requirements people may need to meetInclusion criteria

1. All participants must have Medicare Part A and Part B 2. All participants must be Latino / Hispanic American 3. All participants must be at least 40 years of age 4. All Cancer Screening Group participants must be a Medicare-eligible beneficiary from Region 6 (Central Gulf Coast) as defined by Texas Department of State Health Services. 5. All Cancer Treatment Group participants must have been diagnosed with breast, cervix, prostate, colorectal, and/or lung cancer within the past 5 years. 6. All Cancer Treatment Group participants must be a Medicare-eligible beneficiary from Texas.

Reasons someone may not be able to joinExclusion criteria

1. All participants must not be enrolled in a managed care plan (also called an HMO, Medicare + Choice, or Medicare Advantage) 2. All participants must not be enrolled in hospice 3. All Cancer Screening Group participants must not have been diagnosed with cancer within the last 5 years. 4. All Cancer Treatment Group participants must not be a Medicare-eligible beneficiary outside of Region 6 (Central Gulf Coast) unless treated at MD Anderson.

Important: This is the sponsor’s public criteria, not a determination of eligibility. The study team must review your individual situation.

04
Study sites

U.S. locations

  • University of Texas MD Anderson Cancer CenterHouston, Texas

Source and freshness
Processed from ClinicalTrials.gov. Last public update: Oct 29, 2020. Always confirm current availability with the study team.

View original record ↗