9 Attachment 18-5 and 18-6 BEEA IA/NC Informed Consent Air

FOR IRB USE ONLY
$STAMP_IRB
$STAMP_IRB_ID
$STAMP_APPRV_DT
$STAMP_EXP_DT

Attachment 18.5: BEEA IA Consent Form for Recent Exposed Group–Air Monitoring Home Visit
INFORMED CONSENT DOCUMENT
Project Title:

Biomarkers of Exposures and Effects in Agriculture (BEEA) Study (AMG Home)

Principal Investigator:

Charles Lynch, MD, PhD, The University of Iowa

Research Team Contact:

Deb Lande, Study Coordinator, The University of Iowa

Lead Investigator:

Jonathan Hofmann, PhD, MPH, National Institutes of Health

This consent form describes the research study to help you decide if you want to participate. This form
provides important information about what you will be asked to do during the study, about the risks and
benefits of the study, and about your rights as a research subject.
• If you have any questions about or do not understand something in this form, you should ask the
research team for more information.
• You should discuss your participation with anyone you choose such as family or friends.
• Do not agree to participate in this study unless the research team has answered your questions
and you decide that you want to be part of this study.
WHAT IS THE PURPOSE OF THIS STUDY?
This is a research study. We are inviting you to participate in this research study because you are a
participant in the Agricultural Health Study.
The purpose of this research study is to investigate the changes that may occur in the blood, saliva, and
urine, as well as dust samples from a subset of households when people are exposed to occupational and
environmental chemicals and substances. We are also interested in differences in other body processes
that are affected by lifestyle and the environment. The material in the blood, saliva, and urine samples
will allow us to study these differences in relation to cancer risk, and help understand the causes of
cancer and other chronic diseases.
HOW MANY PEOPLE WILL PARTICIPATE?
Approximately 2200 people in Iowa and North Carolina will take part since this Agricultural Health
Study includes participants from these two states. Of this group approximately 50 people will take part
by completing up to two home visits.
OMB #: 0925-0406
Expiration date: 09/30/2016
Public reporting for this collection of information is estimated to average 5 minutes per response, including the time for reviewing
instructions, searching existing data sources, gathering and maintaining the data needed, and completing and reviewing the collection of
information. An agency may not conduct or sponsor, and a person is not required to respond to, a collection of information unless it
displays a currently valid OMB control number. Send comments regarding this burden estimate or any other aspect of this collection of
information, including suggestions for reducing this burden, to: NIH, Project Clearance Branch, 6705 Rockledge Drive, MSC 7974, Bethesda,
MD 20892-7974, ATTN: PRA (0925-0406). Do not return the completed form to this address.
Page 1 of 6

FOR IRB USE ONLY
$STAMP_IRB
$STAMP_IRB_ID
$STAMP_APPRV_DT
$STAMP_EXP_DT

HOW LONG WILL I BE IN THIS STUDY?
Your involvement for each home visit will be about for 90 minutes. If you agree to take part in the two
home visits, your involvement will be for about 180 minutes total, or 3 hours.
WHAT WILL HAPPEN DURING THIS STUDY?
Study participation will involve completing a maximum of two visits to your home. For each visit, a
trained professional will visit your home to collect blood, saliva, and household dust samples, and the
urine sample you have already collected, and administer a questionnaire that will take about 30 minutes.
The questionnaire will address recent medication use, medical conditions, smoking status, alcohol
consumption, and pesticide use during the current/previous growing season. If a household dust sample
is collected, we will collect your vacuum bag or vacuum waste, and a second questionnaire will apply to
that and should take less than 10 minutes to complete. You are free to skip any questions that you prefer
not to answer. We will collect about 4 tablespoons of blood at each visit. You already have received
mailings and telephone calls from the study field station in order to schedule this home visit.
Tissue/Blood/Data Storage for Future Use
As part of this study, we are obtaining blood, saliva, urine, and household dust samples from you. We
would like to study your samples in the future, after this study is over.
Blood cells removed from the blood samples, and buccal (mouth) cells removed from your saliva, will
likely be used to make a cell line and DNA. Cell lines are produced by growing blood cells in a
laboratory and allow us to have a source of the DNA without having to redraw your blood. The cell lines
and DNA and data will be made available to researchers trying to learn more about the cause of
diseases.
The tests we might want to use to study your blood, saliva, urine, and household dust may not even exist
at this time. Therefore, we are asking for your permission to store your samples so that we can study
them in the future. These future studies may provide additional information that will be helpful in
understanding how occupational and environmental exposures and lifestyle characteristics cause cancer
and other chronic diseases, but it is unlikely that what we learn from these studies will have a direct
benefit to you. It is possible that your blood, saliva, and urine might be used to develop products or tests
that could be patented and licensed. There are no plans to provide financial compensation to you should
this occur.
If you agree now to future use of your blood, saliva, and urine, but decide in the future that you would
like to have it removed from future research, you should contact Dr. Charles Lynch at 319-384-5006.
However, if some research with your blood, saliva, urine, and household dust has already been
completed, the information from that research may still be used.
Audio Recording
One aspect of this study involves making an audio recording of you. This aspect is the computerassisted personal interview. The recording will be used for quality control purposes to ensure we have
correctly captured your responses to the interview questions. It will be destroyed once the quality
Page 2 of 6

FOR IRB USE ONLY
$STAMP_IRB
$STAMP_IRB_ID
$STAMP_APPRV_DT
$STAMP_EXP_DT

control activity is completed.
[ ] Yes

[ ] No

I give you permission to make an audio recording of me during this study.

WHAT ARE THE RISKS OF THIS STUDY?
You may experience one or more of the risks indicated below from being in this study. In addition to
these, there may be other unknown risks, or risks that we did not anticipate, associated with being in this
study.
The physical risks associated with the study are minimal and include those associated with blood
collection. Rarely, there may be swelling or bruising. It is also possible, but very unlikely, that there may
be a risk of loss of confidentiality of your information collected during this study. [
WHAT ARE THE BENEFITS OF THIS STUDY?
You will not benefit from being in this study. However, we hope that, in the future, other people might
benefit from this study because of the knowledge gained.
WILL IT COST ME ANYTHING TO BE IN THIS STUDY?
You will not have any costs for being in this research study.
WILL I RECEIVE A FINANCIAL INCENTIVE FOR PARTICIPATING?
At each home visit, you will receive $100 as a thank you for your participation in this research study. A
personal check in your name for $100 will be provided immediately to you as the phlebotomist
completes the home visit. If you agree to take part in the two home visits, you will receive $300
altogether.
WHO IS FUNDING THIS STUDY?
The Department of Health and Human Services (DHHS) National Institutes of Health (NIH) is funding this
research study. This means that the University of Iowa is receiving payments from DHHS/NIH to support the

activities that are required to conduct the study. No one on the research team will receive a direct
payment or increase in salary from DHHS/NIH for conducting this study.
WHAT IF I AM INJURED AS A RESULT OF THIS STUDY?
•
•
•

If you are injured or become ill from taking part in this study, medical treatment is available at the
University of Iowa Hospitals and Clinics.
The University of Iowa does not plan to provide free medical care or payment for treatment of any
illness or injury resulting from this study unless it is the direct result of proven negligence by a
University employee.
If you experience a research-related illness or injury, you and/or your medical or hospital insurance
carrier will be responsible for the cost of treatment.
Page 3 of 6

FOR IRB USE ONLY
$STAMP_IRB
$STAMP_IRB_ID
$STAMP_APPRV_DT
$STAMP_EXP_DT

WHAT ABOUT CONFIDENTIALITY?
We will keep your participation in this research study confidential to the extent permitted by law.
However, it is possible that other people such as those indicated below may become aware of your
participation in this study and may inspect and copy records pertaining to this research. Some of these
records could contain information that personally identifies you.
• Federal government regulatory agencies,
• Iowa Field Station working with the Agricultural Health Study,
• Auditing departments of the University of Iowa,
• The University of Iowa Institutional Review Board (a committee that reviews and approves
research studies)
• Westat, the Agricultural Health Study coordinating center, and
• NIH, the sponsor.
To help protect your confidentiality, we will provide multiple safeguards. A study number will identify
you in the database. As you can see on the collection containers, a bar code is being used to identify
you. Your consent forms will be stored in securely locked cabinets when not in use. Computerized data
will be entered into password-protected computers, stored in a secure area, and transmitted in a secure
manner. Training sessions and annual signed confidentiality pledges will emphasize and remind
research personnel the importance of keeping all data strictly confidential. If we write a report or article
about this study or share the study data set with others, we will do so in such a way that you cannot be
directly identified. All statistical analyses and publication of study results will involve grouped data.
To further protect your privacy, we have obtained a Certificate of Confidentiality from the National
Institutes of Health. The researchers can use this Certificate to legally refuse to disclose information that
may identify you in any federal, state, or local civil, criminal, administrative, legislative, or other
proceedings, for example, if there is a court subpoena. The researchers will use the Certificate to resist
any demands for information that would identify you, except for the following: The Certificate cannot
be used to resist a demand for information from personnel of the United States federal or state
government agency sponsoring the project and that will be used for auditing or program evaluation of
agency funded projects. You should understand that a Certificate of Confidentiality does not prevent you
or a member of your family from voluntarily releasing information about yourself or your involvement
in this research. If an insurer, medical care provider, or other person obtains your written consent to
receive research information, then the researchers will not use the Certificate to withhold that
information. You may receive a copy of the Certificate of Confidentiality upon request.
IS BEING IN THIS STUDY VOLUNTARY?
Taking part in this research study is completely voluntary. You may choose not to take part at all. If
you decide to be in this study, you may stop participating at any time. If you decide not to be in this
study, or if you stop participating at any time, you won’t be penalized or lose any benefits for which you
otherwise qualify.

Page 4 of 6

FOR IRB USE ONLY
$STAMP_IRB
$STAMP_IRB_ID
$STAMP_APPRV_DT
$STAMP_EXP_DT

WILL I RECEIVE RESEARCH RESULTS?
A clinician on the research team (Dr. Charles Lynch) will review your blood tests red blood cells, white
blood cells, platelets and liver function. If your results indicate something of potential clinical
significance (e.g., anemia or an infection), we will send you a letter with additional information about
the results and recommendations for medical follow-up. The results of this study will be used for
research purposes only and their clinical interpretation is unknown at this time, so we will not be
sending any of the individual results to you.
WHAT IF I HAVE QUESTIONS?
We encourage you to ask questions. If you have any questions about the research study itself, please
call our toll-free number at 1-800-271-1954 and speak to the Study Coordinator, Deb Lande, or ask to
speak with the principal investigator at The University of Iowa, Charles Lynch, MD, PhD at 319-3841558.
If you have questions, concerns, or complaints about your rights as a research subject or about research
related injury, please contact the Human Subjects Office, 105 Hardin Library for the Health Sciences,
600 Newton Road, University of Iowa, Iowa City, Iowa, 52242 -1098, (319) 335-6564, or email [email protected]. General information about being a research subject can be found by clicking “Info
for Public” on the Human Subjects Office web site, http://research.uiowa.edu/hso. To offer input about
your experiences as a research subject or to speak to someone other than the research staff, call the
Human Subjects Office at the number above.

Page 5 of 6

FOR IRB USE ONLY
$STAMP_IRB
$STAMP_IRB_ID
$STAMP_APPRV_DT
$STAMP_EXP_DT

This Informed Consent Document is not a contract. It is a written explanation of what will happen
during the study if you decide to participate. You are not waiving any legal rights by signing this
Informed Consent Document. Your signature indicates that this research study has been explained to
you, that your questions have been answered, and that you agree to take part in this study. You will
receive a copy of this form.
Subject's Name (printed): __________________________________________________________

Do not sign this form if today’s date is on or after $STAMP_EXP_DT.

__________________________________________
(Signature of Subject)

_______________________________
(Date)

Statement of Person Who Obtained Consent
I have discussed the above points with the subject or, where appropriate, with the subject’s legally
authorized representative. It is my opinion that the subject understands the risks, benefits, and
procedures involved with participation in this research study.

__________________________________________
(Signature of Person who Obtained Consent)

_______________________________
(Date)

Page 6 of 6

INFORMED CONSENT DOCUMENT
Attachment 18.6: BEEA NC Consent Form for Recent Exposed Group–Air Monitoring Home Visit
INFORMED CONSENT DOCUMENT
Project Title:

Biomarkers of Exposures and Effects in Agriculture (BEEA) Study

Principal Investigator:

Marsha Dunn, MPH, Westat

Research Team Contact:

Amy Miller, North Carolina Study Coordinator, Westat

Lead Investigator:

Jonathan Hofmann, PhD, MPH, National Institutes of Health

This consent form describes the research study to help you decide if you want to participate. This form
provides important information about what you will be asked to do during the study, about the risks and benefits
of the study, and about your rights as a research subject.
• If you have any questions about or do not understand something in this form, you should ask the
research team for more information.
• You should discuss your participation with anyone you choose such as family or friends.
• Do not agree to participate in this study unless the research team has answered your questions and you
decide that you want to be part of this study.
WHAT IS THE PURPOSE OF THIS STUDY?
This is a research study. We are inviting you to participate in this research study because you are a participant
in the Agricultural Health Study.
The purpose of this research study is to investigate the changes that may occur in the blood, saliva, and urine, as
well as dust samples from a subset of households when people are exposed to occupational and environmental
chemicals and substances. We are also interested in differences in other body processes that are affected by
lifestyle and the environment. The material in the blood, saliva, urine and dust samples will allow us to study
these differences in relation to cancer risk, and help understand the causes of cancer and other chronic diseases.
HOW MANY PEOPLE WILL PARTICIPATE?
Approximately 2,200 people in Iowa and North Carolina will take part since the Agricultural Health Study
includes participants from these two states. Of this group, approximately 50 people will take part by completing
up to two home visits.
HOW LONG WILL I BE IN THIS STUDY?
Your involvement for each home visit will be about for 90 minutes. If you agree to take part in the two home
visits, your involvement will be for about 180 minutes total, or 3 hours.
OMB #: 0925-0406
Expiration date: 09/30/2016
Public reporting for this collection of information is estimated to average 5 minutes per response, including the time for reviewing
instructions, searching existing data sources, gathering and maintaining the data needed, and completing and reviewing the collection of
information. An agency may not conduct or sponsor, and a person is not required to respond to, a collection of information unless it
1 of 5of
displays a currently valid OMB control number. Send comments regarding this burden estimate or any other aspect of thispage
collection
information, including suggestions for reducing this burden, to: NIH, Project Clearance Branch, 6705 Rockledge Drive, MSC 7974,
Bethesda, MD 20892-7974, ATTN: PRA (0925-0406). Do not return the completed form to this address.

WHAT WILL HAPPEN DURING THIS STUDY?
Study participation will involve completing two home visits. For each visit, a trained professional will visit your
home to collect blood, saliva, and household dust samples, and the urine sample you have already collected, and
administer a questionnaire that will take about 30 minutes. The questionnaire will address recent medication
use, medical conditions, smoking status, alcohol consumption, and pesticide use during the current/previous
growing season. If a household dust sample is collected, a second questionnaire will apply to that and should
take less than 10 minutes to complete. You are free to skip any questions that you prefer not to answer. We will
collect about 4 tablespoons of blood at each visit. You already have received mailings and telephone calls from
the study field station in order to schedule the home visit.
Blood/Data Storage for Future Use
As part of this study, we are obtaining blood, saliva, urine and household dust samples from you. We would
like to study your samples in the future, after this study is over.
Blood cells removed from the blood samples, and buccal (mouth) cells removed from your saliva, will likely be
used to make a cell line and DNA. Cell lines are produced by growing blood cells in a laboratory and allow us
to have a source of the DNA without having to redraw your blood. The cell lines and DNA and data will be
made available to researchers trying to learn more about the cause of diseases.
The tests we might want to use to study your blood, saliva, urine, and household dust samples may not even
exist at this time. Therefore, we are asking for your permission to store your samples so that we can study them
in the future. These future studies may provide additional information that will be helpful in understanding how
occupational and environmental exposures and lifestyle characteristics cause cancer and other chronic diseases,
but it is unlikely that what we learn from these studies will have a direct benefit to you. It is possible that your
blood, saliva, and urine might be used to develop products or tests that could be patented and licensed. There
are no plans to provide financial compensation to you should this occur.
If you agree now to future use of your blood, saliva, urine, and dust, but decide in the future that you would like
to have it removed from future research, you should contact Marsha Dunn at 1-800-4AGSTUDY (1-800-4247883). However, if some research with your blood, saliva, urine, and household dust has already been
completed, the information from that research may still be used.
Audio Recording
One aspect of this study involves making an audio recording of you. This aspect is the computer-assisted
personal interview. The recording will be used for quality control purposes to ensure we have correctly
captured your responses to the interview questions. It will be destroyed once the quality control activity is
completed. Research personnel from the North Carolina Field Station, Westat, who are directly involved with
this study will have access to this recording.
[ ] Yes

[ ] No

I give you permission to make an audio recording of me during this study.

WHAT ARE THE RISKS OF THIS STUDY?
You may experience one or more of the risks indicated below from being in this study. In addition to these,
there may be other unknown risks, or risks that we did not anticipate, associated with being in this study.
The physical risks associated with the study are minimal and include those associated with blood collection.
Rarely, there may be swelling or bruising. It is also possible, but very unlikely, that there may be a risk of loss
of confidentiality of your information collected during this study.
page 2 of 5

WHAT ARE THE BENEFITS OF THIS STUDY?
You will not receive any direct benefits from being in this study. However, we hope that, in the future, other
people might benefit from this study because of the knowledge gained.
WILL IT COST ME ANYTHING TO BE IN THIS STUDY?
You will not have any costs for being in this research study.
WILL I RECEIVE A FINANCIAL INCENTIVE FOR PARTICIPATING?
At each home visit, you will receive $100 as a thank you for your participation in this research study. A
personal check in your name will be provided immediately to you as the phlebotomist completes the home visit.
If you agree to take part in the two home visits, you will receive $200 altogether.
WHO IS FUNDING THIS STUDY?
The Department of Health and Human Services (DHHS) National Institutes of Health (NIH) is funding this
research study. This means that Westat is receiving payments from DHHS/NIH to support the activities that are
required to conduct the study. No one on the research team will receive a direct payment or increase in salary
from DHHS/NIH for conducting this study.
WHAT IF I AM INJURED AS A RESULT OF THIS STUDY?
•
•

Westat does not plan to provide free medical care or payment for treatment of any illness or injury resulting
from this study unless it is the direct result of proven negligence by a Westat employee.
If you experience a research-related illness or injury, you and/or your medical or hospital insurance carrier
will be responsible for the cost of treatment.

WHAT ABOUT CONFIDENTIALITY?
We will keep your participation in this research study confidential to the extent permitted by law. However, it
is possible that other people such as those indicated below may become aware of your participation in this study
and may inspect and copy records pertaining to this research. Some of these records could contain information
that personally identifies you.
• Federal government regulatory agencies,
• Westat staff working with the Agricultural Health Study,
• The Westat Institutional Review Board (a committee that reviews and approves research studies), and
• NIH, the sponsor.
To help protect your confidentiality, we will provide multiple safeguards. A study number will identify you in
the database. As you can see on the collection containers, a bar code is being used to identify you. Your
consent forms will be stored in securely locked cabinets when not in use. Computerized data will be entered
into password-protected computers, stored in a secure area, and transmitted in a secure manner. Training
sessions and annual signed confidentiality pledges will emphasize and remind research personnel the
importance of keeping all data strictly confidential. If we write a report or article about this study or share the
study data set with others, we will do so in such a way that you cannot be directly identified. All statistical
analyses and publication of study results will involve grouped data.

page 3 of 5

To further protect your privacy, we have obtained a Certificate of Confidentiality from the National Institutes of
Health. The researchers can use this Certificate to legally refuse to disclose information that may identify you in
any federal, state, or local civil, criminal, administrative, legislative, or other proceedings, for example, if there
is a court subpoena. The researchers will use the Certificate to resist any demands for information that would
identify you, except for the following: The Certificate cannot be used to resist a demand for information from
personnel of the United States federal or state government agency sponsoring the project and that will be used
for auditing or program evaluation of agency funded projects. You should understand that a Certificate of
Confidentiality does not prevent you or a member of your family from voluntarily releasing information about
yourself or your involvement in this research. If an insurer, medical care provider, or other person obtains your
written consent to receive research information, then the researchers will not use the Certificate to withhold that
information. You may receive a copy of the Certificate of Confidentiality upon request.
IS BEING IN THIS STUDY VOLUNTARY?
Taking part in this research study is completely voluntary. You may choose not to take part at all. If you
decide to be in this study, you may stop participating at any time. If you decide not to be in this study, or if you
stop participating at any time, you won’t be penalized or lose any benefits for which you otherwise qualify.
WILL I RECEIVE RESEARCH RESULTS?
A clinician on the research team (Dr. Neil Caporaso) will review your CBC and WBC measurements. If your
results indicate something of potential clinical significance (e.g., anemia or an infection), we will send you a
letter with additional information about the results and recommendations for medical follow-up. The results of
other tests will be used for research purposes only and their clinical interpretation is unknown at this time, so we
will not be sending any other individual results to you.
WHAT IF I HAVE QUESTIONS?
We encourage you to ask questions. If you have any questions about the research study itself, please call our
toll-free number at 1-800-4AGSTUDY (1-800-424-7883) and speak to the Study Coordinator, Amy Miller, or
the principal investigator at Westat, Marsha Dunn. If you experience a research-related injury, please contact:
Marsha Dunn at 1-800-4AGSTUDY.
If you have questions, concerns, or complaints about your rights as a research subject or about research related
injury, please contact the Westat Human Subjects Protections Office, by calling 1-888-920-7631. Please leave a
message with your full name, the name of the research study that you are calling about (the Biomarkers of
Exposures and Effects in Agriculture or BEEA Study), and a phone number beginning with the area code. To
offer input about your experiences as a research subject or to speak to someone other than the research staff, call
the Human Subjects Protections Office at the number above.

page 4 of 5

This Informed Consent Document is not a contract. It is a written explanation of what will happen during the
study if you decide to participate. You are not waiving any legal rights by signing this Informed Consent
Document. Your signature indicates that this research study has been explained to you, that your questions have
been answered, and that you agree to take part in this study. You will receive a copy of this form.
Subject's Name (printed): __________________________________________________________

Do not sign this form if today’s date is on or after ____________________.

__________________________________________
(Signature of Subject)

_______________________________
(Date)

Statement of Person Who Obtained Consent
I have discussed the above points with the subject or, where appropriate, with the subject’s legally authorized
representative. It is my opinion that the subject understands the risks, benefits, and procedures involved with
participation in this research study.

__________________________________________
(Signature of Person who Obtained Consent)

_______________________________
(Date)

page 5 of 5