Agency Forms Undergoing Paperwork Reduction Act Review, 75167-75168 [2012-30563]

Download as PDF Federal Register / Vol. 77, No. 244 / Wednesday, December 19, 2012 / Notices survey, (3) decrease the data collection burden for each PRC by decreasing the number of questions collected on an annual basis, and (4) revise some questions for clarity or to reflect the current needs and priorities of the program. CDC will continue to use the information reported by PRCs to identify training and technical 75167 will report the required information to CDC once per year. The estimated burden per response for the web-based survey will decrease from six hours to five hours, and the estimated burden per response for each telephone interview will decreased from one hour to 30 minutes. There are no costs to respondents other than their time. assistance needs, respond to requests for information from Congress and other sources, monitor grantees’ compliance with cooperative agreement requirements, evaluate progress made in achieving goals and objectives, and describe the impact and effectiveness of the PRC Program. There is no change in the number of respondents (37). Each PRC program ESTIMATED ANNUALIZED BURDEN HOURS Number of responses per respondent Number of respondents Average burden per response (in hours) Total burden (in hours) Type of respondent Form name PRC Program .................................... Survey .............................................. Telephone Interview ......................... 37 37 1 1 5 30/60 185 19 Total ........................................... ........................................................... ........................ ........................ ........................ 204 Dated: December 13, 2012. Ron A. Otten, Director, Office of Scientific Integrity (OSI), Office of the Associate Director for Science (OADS), Office of the Director. [FR Doc. 2012–30562 Filed 12–18–12; 8:45 am] BILLING CODE 4163–18–P DEPARTMENT OF HEALTH AND HUMAN SERVICES Centers for Disease Control and Prevention [30-Day–13–12PS] Agency Forms Undergoing Paperwork Reduction Act Review The Centers for Disease Control and Prevention (CDC) publishes a list of information collection requests under review by the Office of Management and Budget (OMB) in compliance with the Paperwork Reduction Act (44 U.S.C. Chapter 35). To request a copy of these requests, call (404) 639–7570 or send an email to omb@cdc.gov. Send written comments to 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. sroberts on DSK5SPTVN1PROD with Proposed Project Evaluation of the Get Yourself Tested (GYT) Campaign—New—National Center for HIV/AIDS, Viral Hepatitis, STD and TB Prevention (NCHHSTP), Centers for Disease Control and Prevention (CDC). Background and Brief Description The purpose of this data collection is to evaluate the reach and impact of the GYT: Get Yourself Tested campaign. VerDate Mar<15>2010 18:26 Dec 18, 2012 Jkt 229001 Evaluation of GYT will be based on data collected from 4000 young adults. The data will be collected through a 30minute, web-based survey. Data from the survey will then be quantitatively evaluated to determine the reach and impact of the GYT: Get Yourself Tested campaign. This information needs to be collected in order to evaluate whether the GYT: Get Yourself Tested campaign is reaching the appropriate target audience, identify messages the audience is taking away from GYT; determine whether individuals who saw the GYT campaign are more likely to engage in target behaviors and their mediators; and determine whether perceived norms around testing, treatment, and sexual health vary between people who have seen the campaign and those who have not. The information obtained from the proposed data collection will be used by CDC to improve, update and decide whether to continue the GYT campaign and to determine whether GYT is able or unable to impact norms and behaviors related to STD testing. It will also be used to inform future efforts to communicate with the public about STD/HIV testing. Because the GYT campaign targets young adults and minority youth, populations with higher rates of STD/ HIV than the general population, it is essential to examine the effectiveness of this communication to determine whether this campaign is addressing these high STD/HIV rates. If the campaign is not evaluated, there will be no evidence-based criteria which can be used to guide the future of the campaign. Additionally, future efforts to communicate with the public and providers about STD/HIV issues will be PO 00000 Frm 00063 Fmt 4703 Sfmt 4703 hampered by the lack of evidence of this campaign’s effectiveness. CDC, National Association of City and County Health Officials (NACCHO) and Knowledge Networks will disseminate the study results to the public through reports prepared for/by CDC, NACCHO and Knowledge Networks and through peer-reviewed journal articles and related presentations. All releases of information will be reviewed and approved by CDC and partner organizations involved with GYT. This evaluation study will rely on a Web-based survey to be selfadministered at home or at work on personal computers. Using the existing research panel as a population from which to draw a sample of participants has many advantages. First, because the panel is already recruited, consented, and familiar with the technology, there is no burden of recruitment and introduction to the survey method. This saves a great deal of burden on the public and on CDC, as we need not engage in random-digit dialing (RDD) or other sampling procedures to accrue participants, and we need not spend time explaining how to complete the survey. Second, Knowledge Networks has conducted the research to validate the sample and ensure its representativeness. This enhances the generalizability of the study, and thus the value of the results is greater than if we relied on a sample of phonerecruited volunteers. Third, Knowledge Networks has conducted surveys of sensitive and stigmatized topics in the past, including an in-depth and explicit sexual behavior survey. These surveys have been extremely successful. This allows us to proceed with confidence in the method, the contractor, and the survey design. The total annualized E:\FR\FM\19DEN1.SGM 19DEN1 75168 Federal Register / Vol. 77, No. 244 / Wednesday, December 19, 2012 / Notices response burden is estimated at 2000 hours for 4000 web-based surveys. There are no costs to respondents other than their time. ANNUALIZED BURDEN HOURS Respondents Form name Number of respondents Number of responses per respondent Average burden per response (hrs.) Young adults ................................................... Web-based survey ......................................... 4000 1 30/60 Dated: December 13, 2012. Ron A. Otten, Director, Office of Scientific Integrity (OSI), Office of the Associate Director for Science (OADS), Office of the Director, Centers for Disease Control and Prevention. Proposed Project Million HeartsTM Hypertension Control Challenge—New—National Center for Chronic Disease Prevention and Health Promotion (NCCDPHP), Centers for Disease Control and Prevention (CDC). [FR Doc. 2012–30563 Filed 12–18–12; 8:45 am] BILLING CODE 4163–18–P DEPARTMENT OF HEALTH AND HUMAN SERVICES Centers for Disease Control and Prevention [60-Day–13–13EP] sroberts on DSK5SPTVN1PROD with Proposed Data Collections Submitted for Public Comment and Recommendations In compliance with the requirement of Section 3506(c)(2)(A) of the Paperwork Reduction Act of 1995 for opportunity for public comment on proposed data collection projects, the Centers for Disease Control and Prevention (CDC) will publish periodic summaries of proposed projects. To request more information on the proposed projects or to obtain a copy of the data collection plans and instruments, call 404–639–7570 or send comments to Ron Otten, 1600 Clifton Road, MS–D74, Atlanta, GA 30333 or send an email to omb@cdc.gov. 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; and (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. Written comments should be received within 60 days of this notice. VerDate Mar<15>2010 18:26 Dec 18, 2012 Jkt 229001 Background and Brief Description Cardiovascular disease is a leading cause of death for men and women in the United States, among the most costly health problems facing our nation today, and among the most preventable. Heart disease and stroke also contribute significantly to disability. High blood pressure, also known as hypertension, is one of the leading causes of heart disease and stroke. Currently, about 67 million American adults have high blood pressure but fewer than half (46%) have adequately controlled blood pressure. The costs of hypertension and its associated diseases are estimated at $156 billion annually, including the cost of medical care and the cost of lost productivity. In September 2011, CDC launched the Million HeartsTM initiative with the goal of preventing one million heart attacks and strokes by 2017. In order to achieve this goal, at least 10 million more Americans must have their blood pressure under control. Toward this end, Million HeartsTM is promoting clinical practices that are effective in increasing blood pressure control among patient populations. There is scientific evidence that provides general guidance on the types of system-based changes to clinical practice that can improve patient blood pressure control, but more information is needed to fully understand implementation practices so that they can be shared and promoted. In May 2013, CDC proposes to launch the Million HeartsTM Hypertension Control Challenge to identify clinical practices and health systems that have been successful in achieving high rates of hypertension control and to develop models for dissemination. The most successful clinical practices or health plans will be recognized as Million HeartsTM Hypertension Control Champions and will receive a cash PO 00000 Frm 00064 Fmt 4703 Sfmt 4703 award of $5,000–$15,000. Recognition will be provided to two groups of practices: Those that represent fewer than 50,000 covered lives, and those that represent 50,000 or more covered lives. Providers eligible to apply for recognition include single practice providers, group practice providers, and healthcare systems. The Challenge is authorized by Public Law 111–358, the America Creating Opportunities to Meaningfully Promote Excellence in Technology, Education and Science Reauthorization Act of 2010 (COMPETES Act). CDC requests OMB approval to collect the information needed to identify, qualify, and rank applicants for recognition through the Million HeartsTM Hypertension Control Challenge. Interested providers or clinical programs may voluntarily selfnominate their practice or healthcare system by completing a web-based nomination form located on the Challenge.gov web portal. The nomination process will include submission of the minimum amount of data needed to provide evidence of clinical success in achieving hypertension control, including: (a) Two point-in-time measures of the clinical hypertension control rate for the patient population, (b) the size of the clinic population served, and (c) a description of the sustainable systems adopted to achieve hypertension control rates. The estimated burden for completing the nomination form is 30 minutes. CDC scientists or contractors will assign a preliminary score to each submitted nomination form. Those with the highest preliminary scores will be further reviewed by a CDC-sponsored panel of three to five experts in hypertension control. The panel will provide CDC with a ranked list of nominees recommended for recognition through the Million HeartsTM Hypertension Control Challenge. Finalists will be asked to participate in a data verification process so that CDC can verify the information submitted on the nomination form. The estimated burden to the respondent is one hour, which includes time to review E:\FR\FM\19DEN1.SGM 19DEN1

Agencies

[Federal Register Volume 77, Number 244 (Wednesday, December 19, 2012)]
[Notices]
[Pages 75167-75168]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: 2012-30563]


-----------------------------------------------------------------------

DEPARTMENT OF HEALTH AND HUMAN SERVICES

Centers for Disease Control and Prevention

[30-Day-13-12PS]


Agency Forms Undergoing Paperwork Reduction Act Review

    The Centers for Disease Control and Prevention (CDC) publishes a 
list of information collection requests under review by the Office of 
Management and Budget (OMB) in compliance with the Paperwork Reduction 
Act (44 U.S.C. Chapter 35). To request a copy of these requests, call 
(404) 639-7570 or send an email to omb@cdc.gov. Send written comments 
to 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

    Evaluation of the Get Yourself Tested (GYT) Campaign--New--National 
Center for HIV/AIDS, Viral Hepatitis, STD and TB Prevention (NCHHSTP), 
Centers for Disease Control and Prevention (CDC).

Background and Brief Description

    The purpose of this data collection is to evaluate the reach and 
impact of the GYT: Get Yourself Tested campaign. Evaluation of GYT will 
be based on data collected from 4000 young adults. The data will be 
collected through a 30-minute, web-based survey. Data from the survey 
will then be quantitatively evaluated to determine the reach and impact 
of the GYT: Get Yourself Tested campaign.
    This information needs to be collected in order to evaluate whether 
the GYT: Get Yourself Tested campaign is reaching the appropriate 
target audience, identify messages the audience is taking away from 
GYT; determine whether individuals who saw the GYT campaign are more 
likely to engage in target behaviors and their mediators; and determine 
whether perceived norms around testing, treatment, and sexual health 
vary between people who have seen the campaign and those who have not. 
The information obtained from the proposed data collection will be used 
by CDC to improve, update and decide whether to continue the GYT 
campaign and to determine whether GYT is able or unable to impact norms 
and behaviors related to STD testing. It will also be used to inform 
future efforts to communicate with the public about STD/HIV testing.
    Because the GYT campaign targets young adults and minority youth, 
populations with higher rates of STD/HIV than the general population, 
it is essential to examine the effectiveness of this communication to 
determine whether this campaign is addressing these high STD/HIV rates. 
If the campaign is not evaluated, there will be no evidence-based 
criteria which can be used to guide the future of the campaign. 
Additionally, future efforts to communicate with the public and 
providers about STD/HIV issues will be hampered by the lack of evidence 
of this campaign's effectiveness.
    CDC, National Association of City and County Health Officials 
(NACCHO) and Knowledge Networks will disseminate the study results to 
the public through reports prepared for/by CDC, NACCHO and Knowledge 
Networks and through peer-reviewed journal articles and related 
presentations. All releases of information will be reviewed and 
approved by CDC and partner organizations involved with GYT.
    This evaluation study will rely on a Web-based survey to be self-
administered at home or at work on personal computers. Using the 
existing research panel as a population from which to draw a sample of 
participants has many advantages. First, because the panel is already 
recruited, consented, and familiar with the technology, there is no 
burden of recruitment and introduction to the survey method. This saves 
a great deal of burden on the public and on CDC, as we need not engage 
in random-digit dialing (RDD) or other sampling procedures to accrue 
participants, and we need not spend time explaining how to complete the 
survey. Second, Knowledge Networks has conducted the research to 
validate the sample and ensure its representativeness. This enhances 
the generalizability of the study, and thus the value of the results is 
greater than if we relied on a sample of phone-recruited volunteers. 
Third, Knowledge Networks has conducted surveys of sensitive and 
stigmatized topics in the past, including an in-depth and explicit 
sexual behavior survey. These surveys have been extremely successful. 
This allows us to proceed with confidence in the method, the 
contractor, and the survey design. The total annualized

[[Page 75168]]

response burden is estimated at 2000 hours for 4000 web-based surveys.
    There are no costs to respondents other than their time.

                                             Annualized Burden Hours
----------------------------------------------------------------------------------------------------------------
                                                                                   Number of      Average burden
             Respondents                     Form name            Number of      responses per     per response
                                                                 respondents       respondent         (hrs.)
----------------------------------------------------------------------------------------------------------------
Young adults........................  Web-based survey.......            4000                1            30/60
----------------------------------------------------------------------------------------------------------------


    Dated: December 13, 2012.
Ron A. Otten,
Director, Office of Scientific Integrity (OSI), Office of the Associate 
Director for Science (OADS), Office of the Director, Centers for 
Disease Control and Prevention.
[FR Doc. 2012-30563 Filed 12-18-12; 8:45 am]
BILLING CODE 4163-18-P
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