Addressing Disparities in Cancer Care for Latino Medicare Beneficiaries

Not Applicable

Completed

• Conditions: Cancer
• Interventions: Behavioral: cancer screening and health education; Behavioral: facilitation of Services to improve cancer screening

• Registration Number: NCT00385866
• Lead Sponsor: University of Medicine and Dentistry of New Jersey

Brief Summary

To reduce Cancer health care disparities that exists among minority Medicare beneficiaries and to demonstrate cost effectiveness of patient navigation in reducing the burden of cancer.

Detailed Description

The Latino population is the fastest growing minority population in the United States . Cancer ranks as the second leading cause of death among Latinos in the United States (24%), second only to heart disease . This project will evaluate whether an innovative facilitation program (targeting cancers of the prostate, colon/rectum, breast, and cervix) will improve cancer outcomes among Latino Medicare beneficiaries in the city of Newark, New Jersey.

The overall aim of this project is to institute an innovative cancer care facilitation program for elderly Latinos in the city of Newark, NJ. The goal is to reduce the disparities observed in screening, time to diagnosis and treatment services, by utilizing a multidisciplinary team approach to health care, incorporating systems thinking methodology. Using the Multilevel Approach to Community Health (MATCH) planning model , the program will incorporate community outreach, education, and access to screening, and patient assistance in all aspects of the health care continuum. It will also include cultural and linguistic competency training for all those involved in the facilitation process. To accomplish this goal, we propose four objectives:

1. To establish a multidisciplinary team that will utilize a systems thinking approach to design and structure the delivery of cancer screening, diagnosis and treatment facilitation services.

2. To build a collaborative consortium between program partners to improve screening outcomes, that will encourage the utilization of services in the community.

3. To improve the delivery of cancer prevention and treatment facilitation by providing cultural and linguistic competency training to the multidisciplinary team, providers, and the community.

4. To demonstrate the effectiveness of the intervention in reducing the burden of cancer, by increasing screening rates, improving time to diagnosis and delivery of treatment services, patient satisfaction, and appropriate use of Medicare services.

Study Timeline

• Study Start: 2006-10
• Study First Submitted: 2006-10-10
• Study First Submitted QC: 2006-10-10
• Study First Posted: 2006-10-11
• Primary Completion: 2010-09
• Study Completion: 2010-12
• Status Verified: 2016-04
• Last Update Submitted: 2016-04-19
• Last Update Posted: 2016-04-20

Recruitment & Eligibility

• Status: COMPLETED
• Sex: All
• Target Recruitment: 1272

Inclusion Criteria

Cancer-Negative Group

1. Be of Hispanic/Latino Origin
2. Fluent in English and/or Spanish
3. Recipient of, Medicare Part A & B, or combined Medicare/Medicaid
4. Not having a previous diagnosis of cancer
5. Be capable of giving written informed consent prior to any study related procedures.
6. Be available and willing to complete all study assessments as specified.

Cancer-Positive Group

1. Be of Hispanic/Latino Origin
2. Fluent in English and/or Spanish
3. Recipient of, Medicare Part A & B, or combined Medicare/Medicaid
4. Having a previous diagnosis of cancer of the breast, cervix, colon and/or rectum, prostate, or lung.
5. Be capable of giving written informed consent prior to any study related procedures.
6. Be available and willing to complete all study assessments as specified.

Exclusion Criteria

1. Member of the Medicare Advantage Plan, any Medicare managed care plan (Those who join the Medicare Advantage plan or a managed care plan during the course of the study will become ineligible to continue.)
2. Medicaid only beneficiaries
3. Institutionalized
4. Unable to provide written informed consent

Study & Design

• Study Type: INTERVENTIONAL
• Study Design: PARALLEL

Arm && Interventions

Group	Intervention	Description
Intervention group	facilitation of Services to improve cancer screening	The intervention group are those participants who were randomly assigned to receive facilitation of services in the form of patient navigation for the duration of the study.
Comparison Group	cancer screening and health education	The control or lesser intervention group, will receive cancer screening information on a quarterly basis, with no facilitation of services.
Intervention group	cancer screening and health education	The intervention group are those participants who were randomly assigned to receive facilitation of services in the form of patient navigation for the duration of the study.

Primary Outcome Measures

Name	Time	Method
Reduce the disparities observed in utilization of cancer screening services	2-4 years

Secondary Outcome Measures

Name	Time	Method
Improve patient satisfaction and informed decision making.	4 years
Improve the time to diagnosis and treatment services (resulting in reduced cost of cancer care	4 years

Trial Locations

Locations (1)

UMDNJ; 🇺🇸 Newark, New Jersey, United States