INTRODUCTION
The Centers for Disease Control and Prevention (CDC), National Institute
for Occupational Safety and Health (NIOSH), announces the availability
of fiscal year (FY) 1998 funds for the acceptance of grant applications
for research projects relating to occupational safety and health concerns
associated with occupational exposures to radiation and other hazardous
agents at nuclear facilities and in other energy-related industries. Studies
in the nuclear power industry and deliberate exposure of human subjects
in radiation experiments are outside the scope of this announcement.
CDC is committed to achieving the health promotion and disease prevention
objectives of Healthy People 2000, a national activity to reduce
morbidity and mortality and improve the quality of life. This announcement
is related to the priority area of Occupational Safety and Health. (For
ordering a copy of Healthy People 2000, see the section Where
to Obtain Additional Information.)
AUTHORITY
This program is authorized under the Public Health Service Act, as amended,
Section 301(a) [42 U.S.C. 241(a)]; the Occupational Safety and Health Act
of 1970, Section 20 (a) [29 U.S.C. 669(a)]. The applicable program regulations
are in 42 CFR Part 52.
ELIGIBLE APPLICANTS
Eligible applicants include domestic and foreign non-profit and for-profit
organizations, universities, colleges, research institutions, and other
public and private organizations, including State and local governments,
and small, minority and/or woman-owned businesses.
NOTE: Effective January 1, 1996, Public Law 104-65 states that
an organization described in section 501(c)(4) of the Internal Revenue
Code of 1986 which engages in lobbying activities shall not be eligible
to receive Federal funds constituting an award, grant (cooperative agreement),
contract, loan, or any other form.
SMOKE-FREE WORKPLACE
CDC strongly encourages all grant recipients to provide a smoke-free
workplace and promote the non-use of all tobacco products, and Public Law
103-227, the Pro-Children Act of 1994, prohibits smoking in certain facilities
that receive Federal funds in which education, library, day care, health
care, and early childhood development services are provided to children.
AVAILABILITY OF FUNDS
Approximately $500,000 is available in fiscal year (FY) 1998 to fund
approximately 3 to 5 research project grants (R01). The amount of funding
available is subject to change. Awards will range from $50,000 to $200,000
in total costs (direct and indirect) per year. Awards are expected to begin
on or about July 1, 1998. Awards will be made for a 12-month budget period
within a project period not to exceed 3 years. Continuation awards within
the project period will be made on the basis of satisfactory progress and
availability of funds.
USE OF FUNDS
Restrictions on Lobbying
Applicants should be aware of restrictions on the use of HHS funds for
lobbying of Federal or State legislative bodies. Under the provisions of
31 U.S.C. Section 1352 (which has been in effect since December 23, 1989),
recipients (and their subtier contractors) are prohibited from using appropriated
Federal funds (other than profits from a Federal contract) for lobbying
congress or any Federal agency in connection with the award of a particular
contract, grant. cooperative agreement, or loan. This includes grants/cooperative
agreements that, in whole or in part, involve conferences for which Federal
funds cannot be used directly or indirectly to encourage participants to
lobby or to instruct participants on how to lobby.
In addition, the FY 1998 Department of Labor, Health and Human Services,
and Education, and Related Agencies Appropriations Act (Public Law 105-78)
states in Section 503 (a) and (b) that no part of any appropriation contained
in this Act shall be used, other than for normal and recognized executive-legislative
relationships, for publicity or propaganda purposes, for the preparation,
distribution, or use of any kit, pamphlet, booklet, publication, radio,
television, or video presentation designed to support or defeat legislation
pending before the Congress or any State legislature, except in presentation
to the Congress or any State legislature itself. No part of any appropriation
contained in this Act shall be used to pay the salary or expenses of any
grant or contract recipient, or agent acting for such recipient, related
to any activity designed to influence legislation or appropriations pending
before the Congress or any State legislature.
BACKGROUND
The Secretary, Department of Health and Human Services (HHS) and the
Secretary, Department of Energy (DOE) signed a Memorandum of Understanding
(MOU) transferring the authority and resources to manage and conduct energy-related
analytic epidemiologic research from DOE to HHS. This includes the authority,
resources, and responsibility for the design, implementation, analysis,
and scientific interpretation of analytic epidemiologic studies of the
following populations: workers at DOE facilities; other workers potentially
exposed to radiation; and workers exposed to potential hazards resulting
from non-nuclear energy production and use.
The Comprehensive Epidemiologic Data Resource (CEDR) was established
by DOE to serve as a repository for data from epidemiologic studies they
had sponsored prior to transferring this responsibility to CDC. These data
are available to investigators who wish to conduct additional analyses
on these completed studies in response to this announcement. The CEDR is
maintained by DOE and to access the data, an investigator must make an
application to the DOE's Office of Environment, Safety and Health.
PURPOSE
NIOSH will support applied field research projects to identify and investigate
the relationships between health outcomes and occupational exposure to
radiation and other hazardous agents; epidemiologic methods research relevant
to energy-related occupational health research; and research related to
assessing occupational exposures.
PROGRAMMATIC INTEREST
The focus of grants should reflect the following topical areas, emphasizing field research: (1) retrospective exposure assessment, (2) radiation measurement issues, (3) non-cancer morbidity and mortality outcomes, (4) meta-analysis and combined analysis methodologies, (5) uncertainty analysis, (6) effects of measurement error on risk estimates, (7) studies of current workers, and (8) risk communication and worker outreach.
(1) Retrospective Exposure Assessment
Epidemiologic studies of occupational cohorts frequently involve, and can generally benefit from, retrospective exposure assessment to provide estimates of exposure or categorize groups of workers by common exposure. Exposure assessment in energy-related occupational epidemiology requires evaluating exposures to various hazards including ionizing and non-ionizing radiation, metals, acids, and solvents. Grant opportunities encompass the fields of industrial hygiene and retrospective exposure assessment of health physics dosimetry. Research areas of general interest include: methods to use limited data to best advantage; how to treat censored data in retrospective exposure assessment; uncertainty analysis techniques for industrial hygiene exposure data and health physics dosimetry; insight to sampling strategy design yielding a representative understanding of exposed groups; decision logic to select/use the most appropriate exposure metric for epidemiologic and risk assessment use; and, development approaches of "Homogeneous Exposed Groupings" and the advantages/limitations for epidemiologic use. Research opportunities of specific interest include: reconstruction and dose adjustment of historic film badges; exposure assessment for acid mists, carcinogenic solvents, exotic metals, and leukemogens; assessment of electromagnetic field exposure; and evaluation of biomarkers of exposure.
(2) Radiation Measurement Issues
This topic will focus on the applicability and utility of radiation dose data in epidemiological research. Examples of such issues include how to use nondetectable values and missing dose data in historical radiation exposure measurements, the accuracy of historical external dosimetry techniques (film and pocket dosimeters), combining external and internal doses into a useful index, historical bioassay, and radiochemistry techniques.
(3) Non-cancer Morbidity and Mortality Outcomes
The majority of analytical epidemiologic research of health effects of energy-related occupational and environmental exposures has focused historically on the assessment of the association between cancer mortality and exposure to ionizing radiation. Although the importance of this research should not be underestimated, it is essential that other potential adverse health effects, as well as other possible energy-related exposures, be thoroughly evaluated as well. Among these would be the possible effects of radiation on the reproductive, neurologic, and immune systems. Chemical exposures highly prevalent in Department of Energy facilities, such as beryllium and mercury, have also been associated with a variety of disease outcomes, particularly respiratory and neurologic in nature.
(4) Meta-Analysis and Combined Analysis Methodologies
Many of the cohorts at nuclear facilities are not individually large enough to detect statistically significant increases in mortality or incidence for rare cancer types. Methods and/or analyses for combining data across studies, whether in summary form or individual data, are valuable to the research effort involving energy-related health research.
(5) Uncertainty Analysis
Measures of occupational exposure are inherently uncertain. Even when measures of external radiation exposure are generally available, the models used to estimate organ dose, shallow versus deep dose, neutron dose, etc., are subject to error. Measures of dose derived from biological monitoring of urine, feces, blood, etc., are even less precise. Methods for assessing the degree of error in various estimates of exposure to both ionizing radiation as well as other toxic agents (chemicals, EMF, etc.) are desirable.
(6) Effects of Measurement Error on Risk Estimates
Estimation of both bias and imprecision introduced into risk analyses through exposure measurement error have recently received considerable attention. Many of the suggested approaches are very computer intensive. Practical solutions to this problem with regard to the spectrum of epidemiologic designs (cohort, case-control, cross-sectional, etc.) are needed, with particular attention to the nature of exposure measurement in radiation epidemiology.
(7) Studies of Current Workers
Much of the epidemiologic research on nuclear workers conducted at nuclear facilities and other sites has emphasized retrospective studies. More recently new activities involve environmental restoration, waste management and other work that is not related to the design and production of nuclear weapons. Workers are being exposed to radiation and other hazardous agents under conditions and in processes not previously encountered. Exposure assessment, epidemiologic and related studies are needed to evaluate these new conditions and processes and the impact on worker health.
(8) Risk Communication and Worker Outreach
Upon completion of a study, the findings must be presented to the workers
at the site where the study was conducted and to people living in the nearby
community. The communication of study results must be done in a manner
that can be readily understood by all persons who want to know the impact
of a given study, and without the use of highly technical terms and scientific
jargon. To communicate effectively with workers, educational outreach may
be needed to help workers understand the scientific principles and terminology
used in the research. Various types of communications may be required to
reach out to all workers and the effectiveness of these communication modes
must be measured. Methodologies for such evaluations may presently exist
or may have to be developed for this purpose. Evaluation studies of communication
of study findings and health risk communication attempts which indicate
ways to influence worker behavior, demonstrates impact of the research
conducted, or provides insight into better ways to communicate to diverse
audiences is needed. Attention should focus on a process to work with researchers
to ensure that the workers and the public can understand the key research
findings and that the effectiveness of the communication can be measured
objectively.
REPORTING REQUIREMENTS
Progress reports are required annually as part of the continuation application
which is due 75 days prior to the start of the next budget period. The
annual progress reports must contain information on accomplishments during
the previous budget period and plans for each remaining year of the project.
Financial status reports (FSR) are required no later than 90 days after
the end of the budget period. The final performance and financial status
reports are required 90 days after the end of the project period.
The final performance report should include, at a minimum, a statement
of original objectives, a summary of research methodology, a summary of
positive and negative findings, and a list of publications resulting from
the project. Research papers, project reports, or theses are acceptable
items to include in the final report. The final report should stand alone
rather than citing the original application. Three copies of reprints of
publications prepared under the grant should accompany the report.
On or before the expiration date of the grant, the applicant shall submit
study data, with appropriate documentation, to the Comprehensive Epidemiologic
Data Resource (CEDR), maintained by the Department of Energy at the Lawrence
Berkeley Laboratory. This shall include analysis files and separate analytic
files for all relevant study data, including demographic variables, radiation
dosimetry, industrial hygiene, work history, and/or medical records data.
A written report describing each data set and a code book for each data
set shall also be submitted. Information about preparation of CEDR files
can be obtained from Barbara Brooks (DOE Headquarters, 301-903-4674) or
Mark Durst (Lawrence Berkeley Labs, 510-486-4136).
For studies that involve workers as subjects, the applicant shall also be responsible for presenting the study findings to workers and to DOE and DOE contractor staff at all sites where the study was conducted. In addition, a similar presentation will be done in a public meeting to inform workers and people living near the site(s). NIOSH will be responsible for arranging the times and a facility for these presentations. The presentation can be done in person or by a videotape. In the latter case, the applicant will be available by telephone to respond to questions from those in attendance.
EVALUATION CRITERIA
Upon receipt, applications will be reviewed by CDC for completeness
and responsiveness. Applications determined to be incomplete or unresponsive
to this announcement will be returned to the applicant without further
consideration. If the proposed project involves organizations or persons
other than those affiliated with the applicant organization, letters of
support and/or cooperation must be included.
Applications that are complete and responsive to the announcement will
be reviewed by an initial review group and will be determined to be competitive
or non-competitive, based on the review criteria identified below and relative
to other applications received. Applications determined to be non-competitive
will be withdrawn from further consideration and the principal investigator/program
director and the official signing for the applicant organization will be
promptly notified. Applications judged to be competitive will be reviewed
for scientific merit and assigned a priority score. Following initial review
for scientific merit, the applications will receive a secondary review
for programmatic importance.
Review criteria for scientific merit are as follows:
1. Technical significance and originality of proposed project.
2. Appropriateness and adequacy of the study design and methodology proposed to carry out the project.
3. Qualifications and research experience of the Principal Investigator and staff, particularly but not exclusively in the area of the proposed project.
4. Availability of resources necessary to perform the project.
5. Documentation of cooperation from collaborators in the project, where applicable.
6. Adequacy of plans to include both sexes and minorities and their subgroups as appropriate for the scientific goals of the project. (Plans for the recruitment and retention of subjects will also be evaluated.)
7. Appropriateness of budget and period of support.
8. Human Subjects - Procedures adequate for the protection of human
subjects must be documented. Recommendations on the adequacy of protections
include: (1) protections appear adequate and there are no comments to make
or concerns to raise, (2) protections appear adequate, but there are comments
regarding the protocol, (3) protections appear inadequate and the Initial
Review Group has concerns related to human subjects, or (4) disapproval
of the application is recommended because the research risks are sufficiently
serious and protection against the risks are inadequate as to make the
entire application unacceptable.
Review criteria for programmatic importance are as follows:
1. Magnitude of the problem in terms of numbers of workers affected.
2. Severity of the injury or disease in the population.
3. Usefulness to applied technical knowledge in the identification,
evaluation, or control of occupational safety and health hazards on a national
or regional basis.
The following will be considered in making funding decisions:
1. Scientific merit of the proposed project as determined by the initial peer review.
2. Programmatic importance of the project as determined by secondary review.
3. Availability of funds.
4. Program balance among priority areas of this announcement.
EXECUTIVE ORDER 12372 REVIEW
Applications are not subject to the review requirements of Executive
Order 12372.
PUBLIC HEALTH SYSTEM REPORTING REQUIREMENT
This program is not subject to the Public Health System Reporting Requirements.
CATALOG OF FEDERAL DOMESTIC ASSISTANCE NUMBER
The Catalog of Federal Domestic Assistance number is 93.262.
OTHER REQUIREMENTS
Human Subjects
If the proposed project involves research on human subjects, the applicant
must comply with the Department of Health and Human Services Regulations
(45 CFR Part 46) regarding the protection of human subjects. Assurance
must be provided to demonstrate that the project will be subject to initial
and continuing review by an appropriate institutional review committee.
The applicant will be responsible for providing assurance in accordance
with the appropriate guidelines and form provided in the application kit.
In addition, the applicant will be responsible for complying with a NIOSH-DOE
agreement that assures the research protocol is reviewed by the institutional
review committee(s) (if such a committee exists) at each DOE site where
the research will be conducted. This process will be coordinated by the
NIOSH Human Subjects Review Board after the award of the grant.
Travel
In the application, the applicant should allow for appropriate travel
to DOE sites, as established under guidelines developed by NIOSH and DOE.
This includes travel for data collection, and worker/community notification
of study results, at each site included in the study protocol. The applicant
shall include in its proposal the costs of travel to NIOSH in Cincinnati,
Ohio, for the annual meeting of energy-related research extramural partners.
Women and Racial and Ethnic Minorities
It is the policy of the CDC to ensure that women and racial and ethnic
groups will be included in CDC-supported research projects involving human
subjects, whenever feasible and appropriate. Racial and ethnic groups are
those defined in OMB Directive No. 15 and include American Indian or Alaska
Native, Asian, Black or African American, Native Hawaiian or Other Pacific
Islander, and Hispanic or Latino. Applicants shall ensure that women and
racial and ethnic minority populations are appropriately represented in
applications for research involving human subjects. Where clear and compelling
rationale exist that inclusion is not feasible, this situation must be
explained as part of the application. In conducting the review of applications
for scientific merit, review groups will evaluate proposed plans for inclusion
of minorities and both sexes as part of the scientific assessment and assigned
a score. This policy does not apply to research studies when the investigator
cannot control the race, ethnicity and/or sex of subjects. Further guidance
to this policy is contained in the Federal Register, Vol.
60, No. 179, Friday, September 15, 1995, pages 47947-47951.
APPLICATION SUBMISSION AND DEADLINES:
A. Preapplication Letter of Intent
Although not a prerequisite of application, a non-binding letter of
intent-to-apply is requested from potential applicants. The letter should
be submitted to the Grants Management Officer (whose address is reflected
in section B, "Applications"). It should be postmarked no later
than April 24, 1998. The letter should identify the announcement
number, name of principal investigator, and specify the priority area to
be addressed by the proposed project. The letter of intent does not influence
review or funding decisions, but it will enable CDC to plan the review
more efficiently, and will ensure that each applicant receives timely and
relevant information prior to application submission.
B. Applications
Applicants should use Form PHS-398 (OMB Number 0925-0001) and adhere
to the ERRATA Instruction Sheet for Form PHS-398 contained in the Grant
Application Kit. Please submit an original and five copies on or before
June 11, 1998 to: Ron Van Duyne, Grants Management Officer, ATTN:
Joanne Wojcik, Procurement and Grants Office, Centers for Disease Control
and Prevention, (CDC), 255 East Paces Ferry Road, NE., Room 300, MS-E13,
Atlanta, GA 30305.
C. Deadlines
1. Applications shall be considered as meeting a deadline if they are either:
A. Received at the above address on or before the deadline date, or
B. Sent on or before the deadline date to the above address, and received in time for the review process. Applicants should request a legibly dated U.S. Postal Service postmark or obtain a legibly dated receipt from a commercial carrier or the U.S. Postal Service. Private metered postmarks shall not be accepted as proof of timely mailings.
2. Applications which do not meet the criteria above are considered
late applications and will be returned to the applicant.
WHERE TO OBTAIN ADDITIONAL INFORMATION
To receive additional written information call 1-888-GRANTS4. You will
be asked for your name and address and will need to refer to Announcement
98030. You will receive a complete program description, information on
application procedures, and application forms. In addition, this announcement
is also available through the CDC Home Page on the Internet. The address
for the CDC Home Page is (http://www.cdc.gov).
The following documents may provide useful information: NIOSH Occupational
Energy Research Program agenda booklet and/or The DOE Access Handbook:
Conducting Health Studies at Department of Energy Sites may be obtained
from the business management contact listed below.
If you have questions after reviewing the contents of all the documents,
business management information may be obtained from Joanne Wojcik, Grants
Management Specialist, Grants Management Branch, Procurement and Grants
Office, Centers for Disease Control and Prevention (CDC), 255 East Paces
Ferry Road, NE., MS E-13, Atlanta, GA 30305, telephone 404-842-6535; fax:
404-842-6513; Internet: jcw6@cdc.gov.
Programmatic technical assistance may be obtained from Roy M. Fleming,
Sc.D., Director Research Grants Program, National Institute for Occupational
Safety and Health, Centers for Disease Control and Prevention (CDC), 1600
Clifton Road, NE., Building 1, Room 3053, MS-D30, Atlanta, GA 30333, telephone
404-639-3343; fax 404-639-4616; internet: rmf2@cdc.gov.
PLEASE REFER TO ANNOUNCEMENT NUMBER 98030 WHEN REQUESTING INFORMATION
AND SUBMITTING AN APPLICATION.
This and other CDC Announcements can be found on the CDC homepage (http://www.cdc.gov)
under the "Funding" section, as well as on the NIOSH homepage
(/niosh/homepage.html) under "Funding Opportunities/Extramural
Programs." For your convenience, you may be able to retrieve a copy
of the PHS Form 398 from (http://www.nih.gov/grants/funding/phs398/phs398.html).
CDC will not send application kits by facsimile or express mail.
Potential applicants may obtain a copy of "Healthy People 2000"
(Full Report, Stock No. 017-001-00474-0) or "Healthy People 2000"
(Summary Report, Stock No. 017-001-00473-1) through the Superintendent
of Documents, Government Printing Office, Washington, DC 20402-9325, telephone
(202) 512-1800.