Agency Forms Undergoing Paperwork Reduction Act Review, 54982-54983 [2014-21881]

Download as PDF 54982 Federal Register / Vol. 79, No. 178 / Monday, September 15, 2014 / Notices Proposed Project DEPARTMENT OF HEALTH AND HUMAN SERVICES Centers for Disease Control and Prevention [30Day–14–0907] Agency Forms Undergoing Paperwork Reduction Act Review The Centers for Disease Control and Prevention (CDC) has submitted the following information collection request to the Office of Management and Budget (OMB) for review and approval in accordance with the Paperwork Reduction Act of 1995. The notice for the proposed information collection is published to obtain comments from the public and affected agencies. Written comments and suggestions from the public and affected agencies concerning the proposed collection of information are encouraged. Your comments should address any of the following: (a) Evaluate whether the proposed collection of information is necessary for the proper performance of the functions of the agency, including whether the information will have practical utility; (b) Evaluate the accuracy of the agencies estimate of the burden of the proposed collection of information, including the validity of the methodology and assumptions used; (c) Enhance the quality, utility, and clarity of the information to be collected; (d) Minimize the burden of the collection of information on those who are to respond, including through the use of appropriate automated, electronic, mechanical, or other technological collection techniques or other forms of information technology, e.g., permitting electronic submission of responses; and (e) Assess information collection costs. To request additional information on the proposed project or to obtain a copy of the information collection plan and instruments, call (404) 639–7570 or send an email to omb@cdc.gov. Written comments and/or suggestions regarding the items contained in this notice should be directed to the Attention: CDC Desk Officer, Office of Management and Budget, Washington, DC 20503 or by fax to (202) 395–5806. Written comments should be received within 30 days of this notice. Musculoskeletal disorder (MSD) intervention effectiveness in material handling operations—Revision— National Institute for Occupational Safety and Health (NIOSH), Centers for Disease Control and Prevention (CDC). Background and Brief Description NIOSH proposes a 2-year approval to continue a study to assess the effectiveness and cost-benefit of occupational safety and health (OSH) interventions for musculoskeletal disorders (MSD). NIOSH and the Ohio Bureau of Workers Compensation (OBWC) will continue to collaborate on a multi-site intervention study at OBWC-insured companies from 2014–2016. In overview, MSD engineering control interventions (such as stair-climbing, powered hand trucks and powered truck lift gates) will be tested for effectiveness in reducing self-reported back and upper extremity pain among up to 960 employees performing material handling operations in up to 72 establishments using a prospective design (multiple baselines across groups). The costs of the interventions will be funded through existing OBWC funds and participating establishments. This study will provide important information that is not currently available elsewhere on the effectiveness of OSH interventions for workers. The study sub-sample will be volunteer employees at OBWC-insured establishments who perform material handling tasks that are expected to be impacted by the engineering control interventions. It is estimated that there will be up to 960 impacted employees in the recruited establishments, which will be paired according to previous WC loss history and establishment size. This protocol is changed from the previous data collection in that: • A Low Back Functional Assessment is no longer being conducted to increase data collection efficiency. • The study population now includes workers performing material handling tasks in all industries, not just wholesale retail trade. Tested interventions also include a number of material handling engineering controls. These changes were made to increase generalizability of results. • All employers will now receive the intervention immediately, rather than half being randomly selected to receive the intervention six months later. This change was made to increase participation among employers. The main outcomes for this study are self-reported low back pain and upper extremity pain collected using surveys every three months over a two-year period from volunteer material handling workers at participating establishments. Individuals will also be asked to report usage of the interventions and material handling exposures every three months over two years. Individuals will also be asked to complete an annual health assessment survey at baseline, and once annually for two years. In order to maximize efficiency and reduce burden, a choice of web-based or paper survey is proposed for the data collection. All collected information will be used to determine whether there are significant differences in reported musculoskeletal pain and functional back pain score ratios (pre/post intervention scores), while controlling for covariates. Once the study is completed, results will be made available through the NIOSH internet site and peer-reviewed publications. In summary, this study will determine the effectiveness of the tested MSD interventions for material handling workers and enable evidence based prevention practices to be shared with the greatest audience possible. NIOSH expects to complete data collection in 2016. There is no cost to respondents other than their time. The total estimated annual burden hours are 1,364. The ‘‘Self-reported low back pain’’ and ‘‘Self-reported upper extremity pain’’ forms are collected nine times over two years. The ‘‘Self-reported general work environment and health’’ form is collected at baseline, at the end of the first year and at the end of the second year. The informed consent form is collected once at the beginning of the study. The early exit interview is collected once for a limited number of participants. tkelley on DSK3SPTVN1PROD with NOTICES ESTIMATED ANNUALIZED BURDEN HOURS Type of respondents Form name Material handling workers ................ Self-reported low back pain .......................................... Self-reported upper extremity pain ............................... VerDate Mar<15>2010 17:10 Sep 12, 2014 Jkt 232001 PO 00000 Frm 00028 Fmt 4703 Number of respondents Sfmt 4703 E:\FR\FM\15SEN1.SGM 960 960 15SEN1 Number of responses per respondent 4.5 4.5 Average burden per response (in hrs.) 5/60 5/60 54983 Federal Register / Vol. 79, No. 178 / Monday, September 15, 2014 / Notices ESTIMATED ANNUALIZED BURDEN HOURS—Continued Type of respondents Number of respondents Form name Self-reported specific job tasks and safety incidents ... Self-reported general work environment and Health .... Informed Consent Form (Overall Study) ...................... Early Exit Interview ....................................................... Leroy A. Richardson, Chief, Information Collection Review Office, Office of Scientific Integrity, Office of the Associate Director for Science, Office of the Director, Centers for Disease Control and Prevention. [FR Doc. 2014–21881 Filed 9–12–14; 8:45 am] BILLING CODE 4163–18–P DEPARTMENT OF HEALTH AND HUMAN SERVICES Centers for Disease Control and Prevention [60-Day–14–14AYC] tkelley on DSK3SPTVN1PROD with NOTICES Proposed Data Collections Submitted for Public Comment and Recommendations The Centers for Disease Control and Prevention (CDC), as part of its continuing effort to reduce public burden, invites the general public and other Federal agencies to take this opportunity to comment on proposed and/or continuing information collections, as required by the Paperwork Reduction Act of 1995. To request more information on the below proposed project or to obtain a copy of the information collection plan and instruments, call 404–639–7570 or send comments to Leroy A. Richardson, 1600 Clifton Road, MS–D74, Atlanta, GA 30333 or send an email to omb@cdc.gov. Comments submitted in response to this notice will be summarized and/or included in the request for Office of Management and Budget (OMB) approval. Comments are invited on: (a) Whether the proposed collection of information is necessary for the proper performance of the functions of the agency, including whether the information shall have practical utility; (b) the accuracy of the agency’s estimate of the burden of the proposed collection of information; (c) ways to enhance the quality, utility, and clarity of the information to be collected; (d) ways to minimize the burden of the collection of information on respondents, including through the use of automated collection techniques or other forms of information technology; and (e) estimates of capital VerDate Mar<15>2010 17:10 Sep 12, 2014 Jkt 232001 or start-up costs and costs of operation, maintenance, and purchase of services to provide information. Burden means the total time, effort, or financial resources expended by persons to generate, maintain, retain, disclose or provide information to or for a Federal agency. This includes the time needed to review instructions; to develop, acquire, install and utilize technology and systems for the purpose of collecting, validating and verifying information, processing and maintaining information, and disclosing and providing information; to train personnel and to be able to respond to a collection of information, to search data sources, to complete and review the collection of information; and to transmit or otherwise disclose the information. Written comments should be received within 60 days of this notice. Proposed Project Behavioral Risk Factor Surveillance System (BRFSS)—Existing Collection In Use Without an OMB Control Number— National Center for Chronic Disease Prevention and Health Promotion (NCCDPHP)—Centers for Disease Control and Prevention (CDC). Background and Brief Description CDC seeks OMB approval to collect information through the Behavioral Risk Factor Surveillance System (BRFSS). The BRFSS is a system of customized telephone surveys conducted by U.S. states, territories, and the District of Columbia to produce state-level data about health-related risk behaviors, chronic health conditions, use of preventive services, and emerging health issues. Information collection is conducted primarily to support state and local health departments, which plan and evaluate public health programs at the state or sub-state level. Information collected through the BRFSS is also used by the federal government and other entities. Scientific research shows that personal health behaviors play a major role in premature morbidity and mortality. Patterns of behavior that affect health or predict adverse effects PO 00000 Frm 00029 Fmt 4703 Sfmt 4703 960 960 960 106 Number of responses per respondent 4.5 1.5 .5 .5 Average burden per response (in hrs.) 5/60 10/60 5/60 5/60 on health are called behavioral risk factors. For example, lack of physical activity is a behavioral risk factor for obesity, type 2 diabetes, cardiovascular diseases, and other diseases and conditions. Although national estimates of some health risk behaviors among U.S. populations are available, the methods used to produce national estimates do not typically produce the type of detailed information needed to plan and implement public health programs; moreover, national estimates provide only limited insight into regional or state-specific variability in health status and risk factors. Information that is specific to public health jurisdictions is required to guide the administration of public health programs. CDC is requesting OMB approval to conduct information collection for the Behavioral Risk Factor Surveillance System (BRFSS). The BRFSS is a nationwide system of cross-sectional telephone health surveys administered by health departments in states, territories, and the District of Columbia (collectively referred to as states) in collaboration with CDC. The BRFSS produces state-level information primarily on health risk behaviors, health conditions, and preventive health practices that are associated with chronic diseases, infectious diseases, and injury. Information collection is sponsored by CDC under the BRFSS cooperative agreement with states and territories. Under this partnership, questionnaire content is determined by BRFSS state coordinators with technical and methodological assistance provided by CDC. The BRFSS is designed to meet the data needs of individual states and territories. For most states and territories, the BRFSS provides the only sources of data amenable to state and local level health and health risk indicators. Over time it has also developed into an important data collection system that federal agencies rely on for state and local health information and to track national health objectives such as Healthy People. Therefore, although the BRFSS remains primarily a state needs-driven system, E:\FR\FM\15SEN1.SGM 15SEN1

Agencies

[Federal Register Volume 79, Number 178 (Monday, September 15, 2014)]
[Notices]
[Pages 54982-54983]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: 2014-21881]



[[Page 54982]]

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DEPARTMENT OF HEALTH AND HUMAN SERVICES

Centers for Disease Control and Prevention

[30Day-14-0907]


Agency Forms Undergoing Paperwork Reduction Act Review

    The Centers for Disease Control and Prevention (CDC) has submitted 
the following information collection request to the Office of 
Management and Budget (OMB) for review and approval in accordance with 
the Paperwork Reduction Act of 1995. The notice for the proposed 
information collection is published to obtain comments from the public 
and affected agencies.
    Written comments and suggestions from the public and affected 
agencies concerning the proposed collection of information are 
encouraged. Your comments should address any of the following: (a) 
Evaluate whether the proposed collection of information is necessary 
for the proper performance of the functions of the agency, including 
whether the information will have practical utility; (b) Evaluate the 
accuracy of the agencies estimate of the burden of the proposed 
collection of information, including the validity of the methodology 
and assumptions used; (c) Enhance the quality, utility, and clarity of 
the information to be collected; (d) Minimize the burden of the 
collection of information on those who are to respond, including 
through the use of appropriate automated, electronic, mechanical, or 
other technological collection techniques or other forms of information 
technology, e.g., permitting electronic submission of responses; and 
(e) Assess information collection costs.
    To request additional information on the proposed project or to 
obtain a copy of the information collection plan and instruments, call 
(404) 639-7570 or send an email to omb@cdc.gov. Written comments and/or 
suggestions regarding the items contained in this notice should be 
directed to the Attention: CDC Desk Officer, Office of Management and 
Budget, Washington, DC 20503 or by fax to (202) 395-5806. Written 
comments should be received within 30 days of this notice.

Proposed Project

    Musculoskeletal disorder (MSD) intervention effectiveness in 
material handling operations--Revision--National Institute for 
Occupational Safety and Health (NIOSH), Centers for Disease Control and 
Prevention (CDC).

Background and Brief Description

    NIOSH proposes a 2-year approval to continue a study to assess the 
effectiveness and cost-benefit of occupational safety and health (OSH) 
interventions for musculoskeletal disorders (MSD).
    NIOSH and the Ohio Bureau of Workers Compensation (OBWC) will 
continue to collaborate on a multi-site intervention study at OBWC-
insured companies from 2014-2016. In overview, MSD engineering control 
interventions (such as stair-climbing, powered hand trucks and powered 
truck lift gates) will be tested for effectiveness in reducing self-
reported back and upper extremity pain among up to 960 employees 
performing material handling operations in up to 72 establishments 
using a prospective design (multiple baselines across groups). The 
costs of the interventions will be funded through existing OBWC funds 
and participating establishments. This study will provide important 
information that is not currently available elsewhere on the 
effectiveness of OSH interventions for workers. The study sub-sample 
will be volunteer employees at OBWC-insured establishments who perform 
material handling tasks that are expected to be impacted by the 
engineering control interventions. It is estimated that there will be 
up to 960 impacted employees in the recruited establishments, which 
will be paired according to previous WC loss history and establishment 
size. This protocol is changed from the previous data collection in 
that:
     A Low Back Functional Assessment is no longer being 
conducted to increase data collection efficiency.
     The study population now includes workers performing 
material handling tasks in all industries, not just wholesale retail 
trade. Tested interventions also include a number of material handling 
engineering controls. These changes were made to increase 
generalizability of results.
     All employers will now receive the intervention 
immediately, rather than half being randomly selected to receive the 
intervention six months later. This change was made to increase 
participation among employers.
    The main outcomes for this study are self-reported low back pain 
and upper extremity pain collected using surveys every three months 
over a two-year period from volunteer material handling workers at 
participating establishments. Individuals will also be asked to report 
usage of the interventions and material handling exposures every three 
months over two years. Individuals will also be asked to complete an 
annual health assessment survey at baseline, and once annually for two 
years.
    In order to maximize efficiency and reduce burden, a choice of web-
based or paper survey is proposed for the data collection.
    All collected information will be used to determine whether there 
are significant differences in reported musculoskeletal pain and 
functional back pain score ratios (pre/post intervention scores), while 
controlling for covariates. Once the study is completed, results will 
be made available through the NIOSH internet site and peer-reviewed 
publications. In summary, this study will determine the effectiveness 
of the tested MSD interventions for material handling workers and 
enable evidence based prevention practices to be shared with the 
greatest audience possible. NIOSH expects to complete data collection 
in 2016. There is no cost to respondents other than their time. The 
total estimated annual burden hours are 1,364.
    The ``Self-reported low back pain'' and ``Self-reported upper 
extremity pain'' forms are collected nine times over two years. The 
``Self-reported general work environment and health'' form is collected 
at baseline, at the end of the first year and at the end of the second 
year. The informed consent form is collected once at the beginning of 
the study. The early exit interview is collected once for a limited 
number of participants.

                                        Estimated Annualized Burden Hours
----------------------------------------------------------------------------------------------------------------
                                                                                                      Average
                                                                     Number of       Number of      burden per
     Type of  respondents                   Form name               respondents    responses per   response  (in
                                                                                    respondent         hrs.)
----------------------------------------------------------------------------------------------------------------
Material handling workers.....  Self-reported low back pain.....             960             4.5            5/60
                                Self-reported upper extremity                960             4.5            5/60
                                 pain.

[[Page 54983]]

 
                                Self-reported specific job tasks             960             4.5            5/60
                                 and safety incidents.
                                Self-reported general work                   960             1.5           10/60
                                 environment and Health.
                                Informed Consent Form (Overall               960              .5            5/60
                                 Study).
                                Early Exit Interview............             106              .5            5/60
----------------------------------------------------------------------------------------------------------------


Leroy A. Richardson,
Chief, Information Collection Review Office, Office of Scientific 
Integrity, Office of the Associate Director for Science, Office of the 
Director, Centers for Disease Control and Prevention.
[FR Doc. 2014-21881 Filed 9-12-14; 8:45 am]
BILLING CODE 4163-18-P
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