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Socioeconomic Status Related
Cancer Disparities Program (SESRCD)

About SESRCD
What roles do psychologists and other behavioral and social scientists play in
cancer prevention and control in underserved communities? A familiar answer is: they provide
theoretical, research, and evaluation data needed to develop evidence-based interventions. A less
common response is that psychologists and other behavioral and social scientists including
anthropologists, public health experts, social workers, and sociologists are effective resources
and community collaborators in cancer control and prevention efforts. The American Psychological
Association (APA) places value not only on creating and communicating scientific knowledge, but
also on translating and applying that knowledge within local contexts to promote health,
education, and human welfare in traditionally underserved populations and communities.
In 2008, APA entered into a five year, $1.75 million cooperative agreement with
the Centers of Disease Control and Prevention, Division of Cancer Prevention and Control
(CDC-DCPC) to implement the Socioeconomic Status Related Cancer Disparities Program (SESRCD).
Administered through APA’s Office on Socioeconomic Status (OSES), SESRCD is a
broad national strategy to mobilize psychologists and other behavioral and social scientists to
provide community cancer serving organizations and stakeholders with individualized capacity
building assistance (CBA) to access, adopt, adapt, and utilize evidence-/practice-based strategies
that address SES related cancer disparities. SESRCD maintains that irrespective of race,
ethnicity, gender, age, disability, or sexual orientation, socioeconomically disadvantaged
communities are disproportionately affected by cancer and have lower survival rates than their
more socioeconomically affluent counterparts. In order to meet the U.S. Department of Health and
Human Services Healthy People 2010 goal of eliminating cancer health disparities, it is important
to focus on underserved populations that suffer a heavier burden of cancer.
Mission:
To strengthen the capacity of local community cancer serving organizations and
stakeholders to access, adopt, and utilize evidence-/practice-based strategies in order to improve
or initiate cancer prevention, early-detection, and survivorship in socioeconomically
disadvantaged populations.
Goals:
The primary goals of the SESRCD Program are to:
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Establish and maintain the infrastructure and strategic
guidance necessary to support the systematic development and effective implementation of SESRCD
activities.
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Develop and sustain a network of psychologists,
anthropologists, sociologists, public health experts, and other behavioral health scientists
(BSSVs) to provide community cancer serving organizations and stakeholders with individualized
capacity building assistance to access, adopt, adapt, and utilize evidence-/practice-based
strategies in addressing SES related cancer disparities.
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Develop, publish, and disseminate nationwide a professional
development training resource designed to:
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increase participants’ intentions to act on
and/or advocate for systemic organizational climate change that facilitates the initiation or
improvement of professional services to address SES related cancer disparities; and
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provide participants with a process for
carrying out their increased intentions to improve cancer prevention and control among
socioeconomically disadvantaged populations.
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Develop and maintain a web based network of community cancer
serving organizations, stakeholders, and BSSVs to disseminate and translate professional
development training activities into practice.
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History
In 1971, the United States Congress passed the National Cancer Act to advance
the national effort against cancer. Despite advances in the implementation of cancer prevention,
early detection, and treatment strategies, cancer remains the second leading cause of death in the
U.S. today. Furthermore, disparities in cancer incidence and mortality remain. Disparities in
cancer are caused by the complex interplay of social position, economic status, culture, and
environment (NCI, 2002). Socioeconomically disadvantaged individuals disproportionately share the
burden of cancer. Socioeconomic indicators such as income, education, and health insurance
coverage influence cancer risk factors including tobacco use, poor nutrition, physical inactivity,
and obesity (Institute of Medicine, 2003). For all cancers combined, residents of counties in the
U.S. with a greater than 20% poverty rate have a 13% higher death rate in men and 3% higher death
rate in women (Ward et al., 2004).
In response to growing public awareness about health disparities across the
entire health spectrum, the US Department of Health and Human Services made it a goal of Healthy
People 2010 “to eliminate health disparities among segments of the population, including
differences that occur by gender, race or ethnicity, education or income, disability, geographic
location, or sexual orientation.” The Centers of Disease Control and Prevention (CDC) is a leader
in nationwide efforts to fulfill this goal of Healthy People 2010 as it relates specifically to
the burden of cancer. Through the Division of Cancer Prevention and Control (DCPC), CDC works with
national cancer organizations, state health agencies, and other key groups to develop, implement,
and promote effective strategies for preventing and controlling cancer.
In an effort to assist national organizations in developing, enhancing, and
coordinating cancer prevention and control activities specifically for underserved populations,
CDC-DCPC issued program announcement DP08-815: National Organization Activities for Cancer Control
in Underserved Populations in 2008. The American Psychological Association’s Office on
Socioeconomic Status responded to the announcement and was subsequently awarded a cooperative
agreement to implement the Socioeconomic Status Related Cancer Disparities Program (SESRCD).
Modeled after long established APA-CDC collaborations such as the Behavioral and Social Science Volunteer (BSSV)
Program (funded by CDC’s Division on HIV and AIDS Prevention) and the Healthy Lesbian, Gay, Bisexual Students Project
(funded by CDC’s Division on Adolescent School Health), SESRCD is a broad national strategy to
strengthen the capacity of community cancer serving organizations and stakeholders to access,
adopt, adapt, and utilize evidence-/practice-based strategies that address SES-related cancer
disparities in socioeconomically disadvantaged populations.
In line with Healthy People 2010, SESRCD focuses its efforts on
socioeconomically disadvantaged communities that are disproportionately affected by cancer and
have lower survival rates than their more socioeconomically affluent counterparts. Although
national in scope, SESRCD aims to be local in impact. By drawing on the expertise of a diverse
network of behavioral and social scientists, SESRCD will integrate theoretical research knowledge
with real world applications and community action to forge strategic partnerships, mobilize
existing community assets, and use evidence-/practice-based strategies to impact systems that
improve health outcomes and reduce cancer disparities in socioeconomically disadvantaged
communities.
References:
CDC. (2008/2009). Division of Cancer Prevention and Control Facts. Available
online at http://www.cdc.gov/cancer/00_pdf/0809_dcp
c_fs.pdf
National Cancer Institute. (2002). Reducing cancer-related health disparities.
Available online at http://plan2002.cancer.gov/infreduce.htm
Institute of Medicine. (2003). Unequal treatment: confronting racial and ethnic
disparities in healthcare. Washington, DC: National Academy Press.
Singh G.K., B.A. Miller, B.F. Hankey, E.J. Feuer, L.W. Pickle (2002). Changing
area Socioeconomic patterns in U.S. cancer mortality, 1950-1998: Part I – All cancers among men.
Journal of the National Cancer Institute 94(12), 904 – 915.
Ward, E., Jemal, A., Cokkinides, V., Singh, G. K., Cardinez, C., Ghafoor, A.,
and Thun, M. (2004). Cancer disparities by race/ethnicity and socioeconomic status. CA: A
Cancer Journal for Clinicians, 54(2), 78-93.
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Cancer Stats
FACT: “Every year, at least 7 million people die from cancer
[worldwide], more than HIV/AIDS, malaria and tuberculosis combined. And almost half of these
deaths are avoidable.” (WHO, 2007).
FACT: In the United States, 1 in 2 individuals will be
diagnosed with cancer during their lifetime and in 2008 alone 565,650 people were estimated to
have died from cancer. (Ries et al. 2005).
FACT: Socioeconomically disadvantage individuals are
disproportionately affected by cancer in the United States:
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For all cancers combined, residents of counties in the
U.S. with a greater than 20% poverty rate have a 13% higher death rate in men and 3% higher
death rate in women (Ward et al., 2004).
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Among people who develop cancer, the five-year survival
rate is more than 10 percentage points higher for persons who live in affluent census tracts
than for persons who live in poorer census tracts (Singh et al., 2003).
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Regardless of race/ethnicity, men and women whose income
is less than twice the poverty level are much more likely to be current smokers than those
with higher incomes. These disparities result in part from targeted promotion and
advertising by cigarette companies (Singh et al., 2003).
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It has been estimated that between 2.4% and 4.8% of all US
cancer deaths are occupationally related. Most of these deaths are due to lung cancer,
bladder cancer, and mesothelioma. Exposure to many known occupational carcinogens, such as
asbestos, is concentrated among manual and industrial workers, which may contribute to
differences in cancer incidence by socioeconomic status (Singh et al., 2003).
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For the four cancer sites for which screening is widely
recommended or practiced (colorectal, female breast, cervix, and prostate), the proportion of
cases diagnosed at localized stage is lower and the proportion diagnosed at distant stage is
higher in high-poverty compared with low-poverty census tracts (Singh et al., 2003).
FACT: The United States Health and Human Services has made
eliminating all health disparities including cancer disparities a major goal of Healthy People
2010.
References:
Ries, L.A.G, Melbert, D., Krapcho, M., Stinchcomb, D.G., Howlader, N.,
Horner, M.J., Mariotto, A., Miller, B.A., Feuer, E.J., Altekruse, S.F., Lewis, D.R., Clegg, L.,
Eisner, M.P., Reichman, M., Edwards, B.K. (eds). (2008). SEER Cancer Statistics Review,
1975-2005, Bethesda, MD: National Cancer Institute. Available online at http://seer.cancer.gov/csr/1975_2005/index.
html
Singh G.K., Miller B.A., Hankey B.F., Edwards B.K. (2003). Area socioeconomic
variations in U.S. cancer incidence, mortality, stage, treatment, and survival, 1975–1999. NCI
Cancer Surveillance Monograph Series, Number 4. Bethesda, MD: National Cancer
Institute. NIH Publication No. 03-0000. Available online at
http://seer.cancer.gov/publicatio
ns/ses/ses_monograph.pdf
Singh, G.K., Miller, B.A., Hankey, B.F., Feuer, E.J., Pickle, L.W. (2002).
Changing area socioeconomic patterns in U.S. cancer mortality, 1950-1998: Part I – All cancers
among men. Journal of the National Cancer Institute 94(12), 904 – 915.
U.S. Department of Health and Human Services (2000). Healthy people 2010:
Understanding and improving health. 2nd ed. Washington, DC: U.S. Government Printing Office.
Available online at http://www.healthypeople.
gov/Document/tableofcontents.htm#volume1
WHO (2007). The World Health’s Organization’s fight against cancer: Strategies
that prevent, cure, and care. Geneva: WHO Press. Available online at http://www.who.int/ca
ncer/publicat/WHOCancerBrochure2007.FINALweb.pdf
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Cancer and
Health Disparities Resources
CDC:
CDC Department of
Cancer Prevention and Control
CDC National
Comprehensive Cancer Control Program
CDC Health Disparities in Cancer
CDC Office of
Minority Health & Health Disparities (OMHD)
National
Program of Cancer Registries (NPCR)
NCI:
National Cancer
Institute
National Cancer
Institute’s Center to Reduce Cancer Health Disparities
National Cancer Institute Cancer Health Disparities
National Cancer Institute’s Train the Trainer Program
Other Resources:
Cancer Control P.L.A.N.E.T. (Plan, Link, Act, Network with Evidence-based
Tools) links to comprehensive cancer control resources for public health professionals
US Department of Health
& Human Services: The Office of Minority Health
American Cancer Society Statistics
Intercultural Cancer
Council
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News & Events
Professional
Development Training Resource (PDTR) Pilot Workshop: Reducing Cancer Disparities
and Promoting Health Equity Among Socioeconomically Disadvantaged Populations
Starting in August, SESRCD is piloting its Professional Development Training
Resource (PDTR) workshop in Washington, DC, New York, NY, Berlin, MD,
Philadelphia, PA, and Tucson, AZ. The PDTR workshop is a 6-7 hour workshop
for community based organization, comprehensive cancer control coalition,
and health department professionals who want to initiate or improve cancer
prevention or control services for socioeconomically disadvantaged populations.
Learn more about
the workshop, including how to register for an upcoming workshop.
SESRCD Trains Psychologists
and other Behavioral and Social Science Volunteers (BSSVs) in the Fight
Against Cancer Related Health Disparities
SESRCD in Monitor
on Psychology February 2009.
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Publications
SESRCD Brochure
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Contact Us
SESRCD Staff
Rebecca Johnson
Administrative Coordinator
Helena Dagadu, MPH
Program Manager
Keyona King-Tsikata, MPH
Program Director
Office on Socioeconomic Status
American Psychological Association
750 First Street, NE
Washington, DC 20002-4242
Phone: (202) 218-3589
Fax: (202) 336-6198
Email
For more information or questions about the program
contact:
The Socioeconomic Status Related Cancer Disparities Program by email.
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