Agency Forms Undergoing Paperwork Reduction Act Review, 15728-15729 [E9-7789]

Download as PDF 15728 Federal Register / Vol. 74, No. 65 / Tuesday, April 7, 2009 / Notices ANNUAL BURDEN ESTIMATES Number of respondents Instrument IAATP: Trainee Survey Pre-Test Administration ............................................. IAATP: Trainee Survey Follow-Up Administration ........................................... Estimated Total Annual Burden Hours: 300. In compliance with the requirements of Section 506(c)(2)(A) of the Paperwork Reduction Act of 1995, the Administration for Children and Families is soliciting public comment on the specific aspects of the information collection described above. Copies of the proposed collection of information can be obtained and comments may be forwarded by writing to the Administration for Children and Families, Office of Administration, Office of Information Services, 370 L’Enfant Promenade, SW., Washington, DC 20447, Attn: ACF Reports Clearance Officer. E-mail address: infocollection@acf.hhs.gov. All requests should be identified by the title of the information collection. The Department specifically requests comments 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) 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. Consideration will be given to comments and suggestions submitted within 60 days of this publication. Dated: April 2, 2009. Janean Chambers, Reports Clearance Officer. [FR Doc. E9–7841 Filed 4–6–09; 8:45 am] BILLING CODE 4184–01–P Number of responses per respondent 1,200 1,200 1 1 Average burden hours per response 0.15 0.10 Total burden hours 180 120 cancers, and other health problems after being treated for cancer. Research evidence suggests that these elevated risks can be mitigated by healthy lifestyle practices and by undergoing regular medical follow-up and cancer screenings, however, little is known about the factors that motivate or hinder the adoption of recommended cancer prevention and screening behaviors in this population. CDC proposes to conduct a survey of five-year CRC survivors to collect information about knowledge, attitudes, psychosocial factors, health status and behaviors, and utilization of health care services including screening services. Potential survey respondents will be identified through California Cancer Registry records. Each physician associated with one or more CRC patients will be responsible for reviewing a customized list of names to identify patients who should not be contacted for recruitment into the study. Following receipt of physician permission to contact potential participants, and receipt of participant consent, 1,000 respondents will complete a survey of health behaviors. Approximately 900 respondents are expected to complete a selfadministered survey that will be delivered and returned by mail, and 100 respondents are expected to complete the survey by computer-assisted telephone interview, in response to a follow-up call from study staff. OMB clearance is being requested for one year of data collection. Findings from this study will help guide future policies, programs, and interventions developed to enhance and improve the long-term health and well being of cancer survivors. There are no costs to respondents except the time to complete the survey. The total estimated burden hours are 1,095. DEPARTMENT OF HEALTH AND HUMAN SERVICES Centers for Disease Control and Prevention [30Day-09–08BJ] 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 the CDC Reports Clearance Officer at (404) 639–5960 or send an email to omb@cdc.gov. Send written comments to CDC Desk Officer, Office of Management and Budget, Washington, DC or by fax to (202) 395–6974. Written comments should be received within 30 days of this notice. Proposed Project A Study of Primary and Secondary Prevention Behaviors Practiced Among Five-Year Survivors of Colorectal Cancer—New—National Center for Chronic Disease Prevention and Control (NCCDPHP), Centers for Disease Control and Prevention (CDC). Background and Brief Description Colorectal cancer (CRC) is the third most prevalent cancer and the second leading cause of cancer death in both men and women in the United States. In 2004, there were an estimated 145,083 new cases of colorectal cancer diagnosed and 53,580 deaths. However, the five-year relative survival rates of patients diagnosed with CRC have been steadily increasing since 1975 and there are now over one million CRC survivors in the U.S. Despite improved survival rates, CRC survivors are at an elevated risk for cancer recurrence, second primary ESTIMATED ANNUALIZED BURDEN HOURS Number of respondents Type of respondents Form name Physicians ......................................... List of Potential Study Participants .. VerDate Nov<24>2008 17:13 Apr 06, 2009 Jkt 217001 PO 00000 Frm 00040 Fmt 4703 Sfmt 4703 Number of responses per respondent 1,950 E:\FR\FM\07APN1.SGM 1 07APN1 Average burden per response (in hours) 13/60 Total burden (in hours) 423 15729 Federal Register / Vol. 74, No. 65 / Tuesday, April 7, 2009 / Notices ESTIMATED ANNUALIZED BURDEN HOURS—Continued Form name CRC Survivors .................................. Script for CATI Follow-up ................. Survey of Health Behaviors ............. Dated: April 1, 2009. Maryam I. Daneshvar, Acting Reports Clearance Officer, Centers for Disease Control and Prevention. [FR Doc. E9–7789 Filed 4–6–09; 8:45 am] BILLING CODE 4163–18–P DEPARTMENT OF HEALTH AND HUMAN SERVICES Substance Abuse and Mental Health Services Administration Agency Information Collection Activities: Proposed Collection; Comment Request In compliance with Section 3506(c)(2)(A) of the Paperwork Reduction Act of 1995 concerning opportunity for public comment on proposed collections of information, the Substance Abuse and Mental Health Services Administration (SAMHSA) will publish periodic summaries of proposed projects. To request more information on the proposed projects or to obtain a copy of the information collection plans, call the SAMHSA 100 1,000 1 1 Reports Clearance Officer on (240) 276– 1243. Comments are invited on: (a) Whether the proposed collections of information are 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. Proposed Project: 2010 National Survey on Drug Use and Health—(OMB No. 0930–0110)—Revision The National Survey on Drug Use and Health (NSDUH) is a survey of the civilian, non-institutionalized population of the United States 12 years old and older. The data are used to determine the prevalence of use of tobacco products, alcohol, illicit substances, and illicit use of 3/60 40/60 Total burden (in hours) 5 667 prescription drugs. The results are used by SAMHSA, ONDCP, Federal government agencies, and other organizations and researchers to establish policy, direct program activities, and better allocate resources. The 2010 NSDUH will continue conducting a follow-up clinical interview with a subsample of approximately 500 respondents. The design of this study is based on the recommendations from a panel of expert consultants convened by the Center for Mental Health Services (CMHS), SAMHSA, to discuss mental health surveillance data collection strategies. The goal is to create a statistically sound measure that may be used to estimate the prevalence of Serious Mental Illness (SMI) among adults (age 18+). For the 2010 NSDUH, no questionnaire changes are proposed. As with all NSDUH/NHSDA surveys conducted since 1999, the sample size of the survey for 2010 will be sufficient to permit prevalence estimates for each of the fifty states and the District of Columbia. The total annual burden estimate is shown below: Average burden per response (hr.) Responses per respondent Number of responses Household Screening .................................................................................... Interview ......................................................................................................... Clinical Follow-up Interview ........................................................................... Screening Verification .................................................................................... Interview Verification ...................................................................................... Average burden per response (in hours) Number of responses per respondent Number of respondents Type of respondents Total burden (hrs) Dated: April 1, 2009. Elaine Parry, Director, Office of Program Services. [FR Doc. E9–7788 Filed 4–6–09; 8:45 am] BILLING CODE 4162–20–P 17:13 Apr 06, 2009 Jkt 217001 .083 1.0 1.0 0.067 0.067 15,836 67,500 500 362 678 ........................ .......................... 84,876 DEPARTMENT OF HEALTH AND HUMAN SERVICES Administration on Aging Agency Information Collection Activities; Proposed Collection; Comment Request; Semi-Annual and Final Reporting Requirements for Older Americans Act Title IV Discretionary Grant Program AGENCY: ACTION: VerDate Nov<24>2008 1 1 1 1 1 190,800 Send comments to Summer King, SAMHSA Reports Clearance Officer, Room 7–1044, One Choke Cherry Road, Rockville, MD 20857 and e-mail her a copy at summer.king@samhsa.hhs.gov. Written comments should be received within 60 days of this notice. 190,800 67,500 500 5,400 10,125 PO 00000 Administration on Aging, HHS. Notice. Frm 00041 Fmt 4703 Sfmt 4703 SUMMARY: The Administration on Aging (AoA) is announcing an opportunity for public comment on the proposed collection of certain information by the agency. Under the Paperwork Reduction Act of 1995 (the PRA), Federal agencies are required to publish notice in the Federal Register concerning each proposed collection of information, including each proposed extension of an existing collection of information, and to allow 60 days for public comment in response to the notice. This notice solicits comments on the information E:\FR\FM\07APN1.SGM 07APN1

Agencies

[Federal Register Volume 74, Number 65 (Tuesday, April 7, 2009)]
[Notices]
[Pages 15728-15729]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: E9-7789]


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

DEPARTMENT OF HEALTH AND HUMAN SERVICES

Centers for Disease Control and Prevention

[30Day-09-08BJ]


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 
the CDC Reports Clearance Officer at (404) 639-5960 or send an e-mail 
to omb@cdc.gov. Send written comments to CDC Desk Officer, Office of 
Management and Budget, Washington, DC or by fax to (202) 395-6974. 
Written comments should be received within 30 days of this notice.

Proposed Project

    A Study of Primary and Secondary Prevention Behaviors Practiced 
Among Five-Year Survivors of Colorectal Cancer--New--National Center 
for Chronic Disease Prevention and Control (NCCDPHP), Centers for 
Disease Control and Prevention (CDC).

Background and Brief Description

    Colorectal cancer (CRC) is the third most prevalent cancer and the 
second leading cause of cancer death in both men and women in the 
United States. In 2004, there were an estimated 145,083 new cases of 
colorectal cancer diagnosed and 53,580 deaths. However, the five-year 
relative survival rates of patients diagnosed with CRC have been 
steadily increasing since 1975 and there are now over one million CRC 
survivors in the U.S.
    Despite improved survival rates, CRC survivors are at an elevated 
risk for cancer recurrence, second primary cancers, and other health 
problems after being treated for cancer. Research evidence suggests 
that these elevated risks can be mitigated by healthy lifestyle 
practices and by undergoing regular medical follow-up and cancer 
screenings, however, little is known about the factors that motivate or 
hinder the adoption of recommended cancer prevention and screening 
behaviors in this population.
    CDC proposes to conduct a survey of five-year CRC survivors to 
collect information about knowledge, attitudes, psychosocial factors, 
health status and behaviors, and utilization of health care services 
including screening services. Potential survey respondents will be 
identified through California Cancer Registry records. Each physician 
associated with one or more CRC patients will be responsible for 
reviewing a customized list of names to identify patients who should 
not be contacted for recruitment into the study. Following receipt of 
physician permission to contact potential participants, and receipt of 
participant consent, 1,000 respondents will complete a survey of health 
behaviors. Approximately 900 respondents are expected to complete a 
self-administered survey that will be delivered and returned by mail, 
and 100 respondents are expected to complete the survey by computer-
assisted telephone interview, in response to a follow-up call from 
study staff. OMB clearance is being requested for one year of data 
collection.
    Findings from this study will help guide future policies, programs, 
and interventions developed to enhance and improve the long-term health 
and well being of cancer survivors.
    There are no costs to respondents except the time to complete the 
survey. The total estimated burden hours are 1,095.

                                        Estimated Annualized Burden Hours
----------------------------------------------------------------------------------------------------------------
                                                                     Number of    Average burden
      Type of respondents           Form name        Number of     responses per   per response    Total burden
                                                    respondents     respondent      (in hours)      (in hours)
----------------------------------------------------------------------------------------------------------------
Physicians....................  List of                    1,950               1           13/60             423
                                 Potential Study
                                 Participants.

[[Page 15729]]

 
CRC Survivors.................  Script for CATI              100               1            3/60               5
                                 Follow-up.
                                Survey of Health           1,000               1           40/60             667
                                 Behaviors.
----------------------------------------------------------------------------------------------------------------


    Dated: April 1, 2009.
Maryam I. Daneshvar,
Acting Reports Clearance Officer, Centers for Disease Control and 
Prevention.
 [FR Doc. E9-7789 Filed 4-6-09; 8:45 am]
BILLING CODE 4163-18-P
This site is protected by reCAPTCHA and the Google Privacy Policy and Terms of Service apply.