Frequently asked questions top
What is the Spit for the Cure Breast Cancer Cohort? What is a Cohort?
Who can participate? Why can't men spit?
What do I do once I
enroll? How long does it take?
How do the questions you ask relate to
breast cancer? Will you know if I am at increased risk for breast cancer?
Why collect saliva? What is DNA?
How does my DNA help with breast
cancer research? What happens to my saliva/DNA?
Why spit instead of
swab? What type of recontact and how often?
Can I still participate if
I don't want to be followed? Can my family participate?
How is my
identity protected? Where can I participate?
Do you want to contact us?
What is the Spit for the
Cure Breast Cancer Cohort? Spit for the Cure is a breast cancer research
study currently led by Martha Phillips, Ph.D., and conducted at the Fay W.
Boozman College of Public Health and Winthrop P. Rockefeller Cancer
Institute at UAMS. Spit for the Cure began as an idea initiated by Susan
Kadlubar, Ph.D., and Suzanne Klimberg, M.D., from UAMS. While driving back
from a conference during the summer of 2007, these investigators began
brainstorming new ways to address breast cancer research in Arkansas. What
they came up with was a unique way to invite women of Arkansas to personally
contribute to the fight against breast cancer. In 2007, we teamed up
with our local Susan G. Komen Arkansas Affiliate to launch our recruiting
efforts with events associated with the Arkansas Susan G. Komen Race for the
Cure ® . Women from all over the state of Arkansas took this unique
opportunity to be involved and became pioneers in breast cancer research.
Today, Spit for the Cure includes over 10,000 women and represents every
county in Arkansas. Our recruiters have attended breast cancer awareness
events, community health fairs, and faith-based events throughout the state.
We work with the Winthrop P. Rockefeller Cancer Institute Arkansas Cancer
Control Network, our local Susan G. Komen for the Cure® Affiliates (Arkansas
and Ozark), the Arkansas State Health Department BreastCare program, and
many other cancer prevention and educational organizations in Arkansas. The
Spit for the Cure Breast Cancer Cohort is continuing to expand and develop
into a comprehensive representation of the women of Arkansas.
What is
a Cohort? Our study literature refers to the "Spit for the Cure Breast
Cancer Cohort". So what is a cohort? In public health studies, a cohort
refers to a group of participants who share a common trait or experience
(such as gender or age). Cohorts are usually followed by researchers for a period of time as part of the study. That is why it is
so important for us to receive regular updates from each participant.
Who can participate? Women between the ages of 18-100 are eligible to
enroll in Spit for the Cure.
Why can't men spit? Due to the low
occurrence of breast cancer in men, we are not recruiting male participants
at this time. What do I do once I enroll? At the time of
enrollment we ask women to sign a consent form, provide a saliva sample for DNA extraction and
answer a short questionnaire. Individuals willing to be recontacted will
receive follow-up materials from study staff asking questions concerning
their health over the next 30 years.
Participation is completely voluntary. You may withdraw from the study at any
time. If you decide not to participate in this study, it will not affect your
medical care now or in the future.
How long does it take? For
most women, it takes about 10-15 minutes to complete the process of
providing consent, providing a saliva sample and answering the questionnaire.
How do the
questions you ask relate to breast cancer? On the questionnaire we ask
questions relating to demographics, personal and/or family history of breast
cancer, and lifestyle choices. We then use a unique identifying barcode to
link this to the information gathered from your DNA. Knowing this
information can guide our research in the future. It also allows us to
development more in-depth follow up questionnaires.
Will you know if
I am at increased risk for breast cancer? As women, we are all at risk to
develop breast cancer, especially as we age. Through this research we hope
to identify factors that put women at increased risk for breast cancer. We
also hope to find out more about why some women respond to treatment and
others do not. We are not searching for the known "breast cancer
genes" (BRCA1/BRCA2) specifically. What we are trying to do is determine how
the traits you inherited from your mother and your father affect the way you
react to your environment. Our researchers are looking for new
gene-environment interactions. We look at differences and make
comparisons in DNA and questionnaire data from the cohort as a whole. That
means we analyze your information as part of a large group and do not look
at individual results. Therefore, we will not be identifying
individuals who are at an increased risk for breast cancer.
Why collect saliva? Most researchers still
use white blood cells from blood to collect DNA. While this has been an
accepted method for several decades, advances in technology have given us
the ability to collect and remove DNA from the white blood cells in saliva.
Not only is the collection of saliva a simple, pain-free process, but it
also aids in our ability to reach individuals in their own communities and
during large events like the Susan G. Komen Race for the Cure®.
What
is DNA? DNA contains all the genetic information that defines who
we are as individuals and it is nature's mechanism for
controlling how all living things function. There has been an
increasing focus over the past decade or so to understand better how DNA
controls the human body. The most significant research initiative in this
regard was The Human Genome Project. This study resulted in a mapping of the
human DNA (which contains 3 billion bits of information in every cell). This
mapping has accelerated interest into further research on how DNA impacts
individual health conditions across almost every type of disease.
How does my DNA help with breast cancer research? In order to
answer questions that relate inherited traits to environmental triggers,
researchers need samples from thousands of women. The more DNA samples we
are able to quickly attain, the faster we will be able to advance our
scientific findings. We hope the information we find in DNA linked to
answers from the questionnaire will give us more insight into what affects
breast cancer risk or treatment options for women in the South.
What
happens to my saliva/DNA? After you provide your saliva sample,
recruiters take the sample back to UAMS where it is stored until enough
samples are collected for processing. Then we extract or remove DNA from the
white blood cells found within the saliva. Finally, the DNA is tested to
determine which genes or parts of genes are present. Researchers can then
link the questionnaires and genetic data to begin addressing
gene-environment interactions.
If you decide to withdraw from the study, your information, including the
information from your saliva sample, will be pulled out of the research data and
will not be used at all. Withdrawing from the study will not affect your medical
care now or in the future.
Why spit instead of a swab? You
may have seen TV shows like CSI where investigators use a swab to collect a
DNA sample from inside the cheek. Or perhaps you have been to a doctor's
office where they use a swab for the collection of DNA. This method is
useful; however, it may lead to contamination by bacteria in your mouth.
Saliva actually has fewer bacterial contaminants than the lining of your
cheek. Collecting saliva allows us to preserve and store samples until we
assemble enough samples for processing.
What type of recontact and
how often? Researchers developing Spit for the Cure are comparing your
genetic make-up, or traits you inherited from your parents, and the way
those traits interact with your environment. Participants in the study will
be followed by investigators for a period of time to address these questions
properly. That is why it is so important for us to send out and receive
regular updates from each participant. These updates should occur
every six to twelve months. The questions are likely to relate to your
current contact information, your health, and more detailed questions
concerning specific risk factors or treatment options for survivors.
There will be multiple ways for you to respond to these requests for
updated information: through the mail, by phone, during repeat recruiting
events, as well as through our website.
Providing your updated information, just like your enrollment in the study
itself, is completely voluntary and will not affect your medical care now or in
the future.
Can I still participate if I
don't want to be followed? At this time we are allowing women between the
ages of 18-100 to participate, regardless of whether or not they are
interested in future follow-up.
Can my family
participate? Yes! We encourage blood relatives to participate. When
family members enroll it allows researchers to look at unique questions
relating to similar genes and environmental exposures.
How is my
identity protected? DNA samples and answers from the questionnaire will
be used to create a "bank" of information for future studies. After
enrollment, we label all of your materials with an ID number connected to a
barcode. This allows us to link your information from the questionnaire and
DNA without using your name or contact information. All of your contact
information is kept in a separate, password protected, secure database. We
do not give out your personal contact information. Researchers will need to
access the samples and data to address specific questions related to the
factors affecting breast cancer risk and treatment. They will do this
through use of the unique ID numbers associated with the samples and data.
This prevents access to any information that could identify you as a person.
Where can I participate?
Spit for the Cure recruiters will be
available throughout Arkansas at the following events:
Click here to visit our
Calendar Page
Individuals may contact us directly:
Back to top
UAMS
Department of
Epidemiology
4301 W. Markham, Slot 820-3, Little Rock, AR 72205 5 01-526-7585
All contents © 2000 -
UAMS Online Copyright Statement Privacy Statement