Agency Information Collection Activities: Proposed Collection; Comment Request, 44942-44944 [2011-18941]
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Federal Register / Vol. 76, No. 144 / Wednesday, July 27, 2011 / Notices
Licensing Status: Available for
licensing.
Licensing Contact: Jennifer Wong;
301–435–4633; wongje@mail.nih.gov.
Collaborative Research Opportunity:
The Center for Cancer Research, Vaccine
Branch, is seeking statements of
capability or interest from parties
interested in collaborative research to
further develop, evaluate, or
commercialize Oral Delivery of a
Vaccine to the Large Intestine to Induce
Mucosal Immunity. Please contact John
Hewes, Ph.D. at 301–435–3121 or
hewesj@mail.nih.gov for more
information.
Dated: July 21, 2011.
Richard U. Rodriguez,
Director, Division of Technology Development
and Transfer, Office of Technology Transfer,
National Institutes of Health.
[FR Doc. 2011–18965 Filed 7–26–11; 8:45 am]
BILLING CODE 4140–01–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
National Institutes of Health
Center for Scientific Review; Notice of
Closed Meetings
sroberts on DSK5SPTVN1PROD with NOTICES
Pursuant to section 10(d) of the
Federal Advisory Committee Act, as
amended (5 U.S.C. App.), notice is
hereby given of the following meetings.
The meetings will be closed to the
public in accordance with the
provisions set forth in sections
552b(c)(4) and 552b(c)(6), Title 5 U.S.C.,
as amended. The grant applications and
the discussions could disclose
confidential trade secrets or commercial
property such as patentable material,
and personal information concerning
individuals associated with the grant
applications, the disclosure of which
would constitute a clearly unwarranted
invasion of personal privacy.
Name of Committee: Center for Scientific
Review Special Emphasis Panel; Member
Conflict: Sensation and Perception.
Date: August 17–18, 2011.
Time: 8 a.m. to 5 p.m.
Agenda: To review and evaluate grant
applications.
Place: National Institutes of Health, 6701
Rockledge Drive, Bethesda, MD 20892
(Virtual Meeting).
Contact Person: John Bishop, PhD,
Scientific Review Officer, Center for
Scientific Review, National Institutes of
Health, 6701 Rockledge Drive, Room 5182,
MSC 7844, Bethesda, MD 20892, (301) 408–
9664, bishopj@csr.nih.gov.
Name of Committee: Center for Scientific
Review Special Emphasis Panel; ADHD and
Brain Development.
Date: August 19, 2011.
Time: 1 p.m. to 3:30 p.m.
VerDate Mar<15>2010
17:08 Jul 26, 2011
Jkt 223001
Agenda: To review and evaluate grant
applications.
Place: National Institutes of Health, 6701
Rockledge Drive, Bethesda, MD 20892
(Telephone Conference Call)
Contact Person: Samuel C. Edwards, PhD,
Chief, Center for Scientific Review, National
Institutes of Health, 6701 Rockledge Drive,
Room 5210, MSC 7846, Bethesda, MD 20892,
(301) 435–1246, edwardss@csr.nih.gov.
Name of Committee: Center for Scientific
Review Special Emphasis Panel; Member
Conflict: Kidney and Urological Diseases.
Date: August 24, 2011.
Time: 2 p.m. to 5 p.m.
Agenda: To review and evaluate grant
applications.
Place: National Institutes of Health, 6701
Rockledge Drive, Bethesda, MD 20892,
(Telephone Conference Call)
Contact Person: Chantal A Rivera, PhD,
Scientific Review Officer, Center for
Scientific Review, National Institutes of
Health, 6701 Rockledge Drive, Room 2186,
MSC 7818, Bethesda, MD 20892, 301–435–
1243, riveraca@mail.nih.gov.
(Catalogue of Federal Domestic Assistance
Program Nos. 93.306, Comparative Medicine;
93.333, Clinical Research, 93.306, 93.333,
93.337, 93.393–93.396, 93.837–93.844,
93.846–93.878, 93.892, 93.893, National
Institutes of Health, HHS)
Dated: July 21, 2011.
Anna P. Snouffer,
Deputy Director, Office of Federal Advisory
Committee Policy.
[FR Doc. 2011–18969 Filed 7–26–11; 8:45 am]
BILLING CODE 4140–01–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
National Institutes of Health
Center for Scientific Review; Notice of
Closed Meeting
Pursuant to section 10(d) of the
Federal Advisory Committee Act, as
amended (5 U.S.C. App.), notice is
hereby given of the following meeting.
The meeting will be closed to the
public in accordance with the
provisions set forth in sections
552b(c)(4) and 552b(c)(6), Title 5 U.S.C.,
as amended. The grant applications and
the discussions could disclose
confidential trade secrets or commercial
property such as patentable material,
and personal information concerning
individuals associated with the grant
applications, the disclosure of which
would constitute a clearly unwarranted
invasion of personal privacy.
Name of Committee: Center for Scientific
Review Special Emphasis Panel; Molecular
Neuroscience.
Date: August 5, 2011.
Time: 12 p.m. to 2 p.m.
Agenda: To review and evaluate grant
applications.
PO 00000
Frm 00055
Fmt 4703
Sfmt 4703
Place: National Institutes of Health, 6701
Rockledge Drive, Bethesda, MD 20892
(Telephone Conference Call)
Contact Person: Toby Behar, PhD,
Scientific Review Officer, Center for
Scientific Review, National Institutes of
Health, 6701 Rockledge Drive, Room 4136,
MSC 7850, Bethesda, MD 20892, (301) 435–
4433, behart@csr.nih.gov.
This notice is being published less than 15
days prior to the meeting due to the timing
limitations imposed by the review and
funding cycle.
(Catalogue of Federal Domestic Assistance
Program Nos. 93.306, Comparative Medicine;
93.333, Clinical Research, 93.306, 93.333,
93.337, 93.393–93.396, 93.837–93.844,
93.846–93.878, 93.892, 93.893, National
Institutes of Health, HHS)
Dated: July 21, 2011.
Anna P. Snouffer,
Deputy Director, Office of Federal Advisory
Committee Policy.
[FR Doc. 2011–18968 Filed 7–26–11; 8:45 am]
BILLING CODE 4140–01–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
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.
E:\FR\FM\27JYN1.SGM
27JYN1
sroberts on DSK5SPTVN1PROD with NOTICES
Federal Register / Vol. 76, No. 144 / Wednesday, July 27, 2011 / Notices
Cross-Site Evaluation of the Minority
Substance Abuse/HIV Prevention
Program—(OMB No. 0930–0298)—
Revision
The Substance Abuse and Mental
Health Services Administration
(SAMHSA), Center for Substance Abuse
Prevention (CSAP) is requesting from
the Office of Management and Budget
(OMB) approval for the revision of data
collection activities for the cross-site
study of the Minority HIV/AIDS
Initiative (MAI), which includes both
youth and adult questionnaires. This
revision includes the addition of 4
cohorts, changes to the data collection
procedures based on intervention
duration, and the addition of two
questions on binge drinking behavior.
The current approval is under OMB No.
0930–0298, which expires on 4/30/12.
This cross-site evaluation supports
two of SAMHSA’s 8 Strategic Initiatives:
Prevention of Substance Abuse and
Mental Illness and Data, Outcomes, and
Quality. It builds on six previous grant
programs funded by SAMHSA’s CSAP
to provide substance abuse and HIV
prevention services for minority
populations. The first two were
planning grant programs and the last
four were service grant programs. The
goals for the Cohort 3–6 grants were to
add, increase, or enhance integrated
substance abuse (SA) and HIV
prevention services by providing
supportive services and strengthening
linkages between service providers for
at-risk minority populations. The HIV
Cohort 1–3 previously received
clearance under OMB No. 0930–0208
and Cohort 6 grants previously received
clearance under OMB No. 0930–0298.
Since neither the HIV Cohort 4 nor the
Cohort 5 Programs were cross-site
studies, they did not require OMB
clearance. The current HIV Minority
SA/HIV Prevention Program funded:
• Cohorts 7 and 8 Prevention of
Substance Abuse (SA) and HIV for AtRisk Racial/Ethnic Minority
Subpopulations Cooperative
Agreements—60 grants for 5 years,
• Cohort 9 Ready-To-Respond
Initiative—35 grants for 5 years, and
• Cohort 10 Capacity Building
Initiative—27 grants for 5 years.
Grantees are community based
organizations that are required to
address the SAMSHA Strategic
Prevention Framework (SPF) and
participate in this cross-site evaluation.
VerDate Mar<15>2010
17:08 Jul 26, 2011
Jkt 223001
The grantees are expected to provide
leadership and coordination on the
planning and implementation of the
SPF that targets minority populations,
the minority reentry population, as well
as other high risk groups residing in
communities of color with high
prevalence of SA and HIV/AIDS. The
primary objectives of the cross-site
study are to: (1) Determine the success
of the MAI in preventing, delaying, and/
or reducing the use of alcohol, tobacco,
and other drugs (ATOD) among the
target populations. The results of this
cross-site study will assist SAMHSA/
CSAP in promoting and disseminating
optimally effective prevention
programs; (2) Measure the effectiveness
of evidence-based programs and
infrastructure development activities
such as: Outreach and training,
mobilization of key stakeholders,
substance abuse and HIV/AIDS
counseling and education, referrals to
appropriate medical treatment and/or
other intervention strategies (i.e.,
cultural enrichment activities,
educational and vocational resources,
and computer-based curricula); and (3)
Assess the process of adopting and
implementing the Strategic Prevention
Framework (SPF) with the target
populations.
The grantees are expected to provide
an effective prevention process,
direction, and a common set of goals,
expectations, and accountabilities to be
adapted and integrated at the
community level. While the grantees
have substantial flexibility in choosing
their individual evidence-based
programs, they are all required to base
them on the five steps of the SPF to
build service capacity specific to SA
and HIV prevention services.
Conducting this cross-site evaluation
will assist SAMHSA/CSAP in
promoting and disseminating optimally
effective prevention programs.
Grantees must also conduct ongoing
monitoring and evaluation of their
projects to assess program effectiveness
including Federal reporting of the
Government Performance and Results
Act (GPRA) of 1993, SAMHSA/CSAP
National Outcome Measures (NOMs),
and HIV Counseling and Testing. All of
this information will be collected
through self-report questionnaires
administered to program participants.
All grantees will use two instruments,
one for youth aged between 12 and 17
PO 00000
Frm 00056
Fmt 4703
Sfmt 4703
44943
and one for adults aged 18 and older.
Participants in interventions lasting 30
days or longer will complete
questionnaires three times, taking an
average of 50 minutes for baseline, exit,
and follow-up questionnaires.
Participants in interventions lasting 2–
29 days will complete questionnaires
two times taking an average of 30
minutes to complete. Single-session
intervention participants will complete
one questionnaire at exit only. The
GPRA and NOMs measures on the
instruments have already been approved
by OMB (OMB No. 0930–0230), and the
remaining HIV-related questions have
been approved under OMB No. 0930–
0298.The youth questionnaire contains
125 questions, of which 28 relate to
HIV/AIDS and the adult questionnaire
contains 118 items, 47 of which relate
to HIV/AIDS. Two additional questions
have been added to address SAMHSA’s
need to collect information on binge
drinking behavior.
These questions are:
1. Females only: During the past 30
days, on how many days did you have
4 or more drinks on the same occasion?
2. Males only: During the past 30
days, on how many days did you have
5 or more drinks on the same occasion?
Sample size, respondent burden, and
intrusiveness have been minimized to
be consistent with the cross-site
objectives. Procedures are employed to
safeguard the privacy and
confidentiality of participants. Every
effort has been made to coordinate
cross-site data collection with local data
collection efforts in an attempt to
minimize respondent burden.
The cross-site evaluation results will
have significant implications for the
substance abuse and HIV/AIDS
prevention fields, the allocation of grant
funds, and other evaluation activities
conducted by multiple Federal, State,
and local government agencies. They
will be used to develop Federal policy
in support of SAMHSA/CSAP program
initiatives, inform the public of lessons
learned and findings, improve existing
programs, and promote replication and
dissemination of effective prevention
strategies.
Total Estimates of Annualized Hour
Burden
The following table shows the
estimated annualized burden for data
collection.
E:\FR\FM\27JYN1.SGM
27JYN1
44944
Federal Register / Vol. 76, No. 144 / Wednesday, July 27, 2011 / Notices
TABLE 1A—ESTIMATES OF ANNUALIZED HOUR BURDEN BY INTERVENTION LENGTH
Number of
respondents
Intervention length
Responses
per
respondent
Total
responses
Hours per
response
Total hour
burden
30-Day or More Intervention
Baseline ...............................................................................
Exit .......................................................................................
Follow-up ..............................................................................
7,937
4,887
2,942
1
1
1
7,937
4,887
2,942
0.83
0.83
0.83
6,588
4,056
2,442
Subtotal .........................................................................
7,937
........................
15,766
........................
13,086
2- to 29-Day Intervention
Baseline ...............................................................................
Exit .......................................................................................
1,416
872
1
1
1,416
872
0.5
0.5
708
436
Subtotal .........................................................................
1,416
........................
2,288
........................
1,144
Single Day Intervention
Exit .......................................................................................
2,458
1
2,458
0.25
614
Annualized Total ...........................................................
11,811
........................
20,512
........................
14,844
TABLE 1B—ESTIMATES OF ANNUALIZED HOUR BURDEN BY SURVEY TYPE
Number of
respondents
Questionnaire
Total
responses
Total hour
burden
Annualized Total Adult .................................................................................................................
Annualized Total Youth ...............................................................................................................
9,682
2,128
16,899
3,612
12,234
2,610
Annualized Total ...................................................................................................................
11,811
20,512
14,844
Send comments to Summer King,
SAMHSA Reports Clearance Officer,
Room 8–1099, One Choke Cherry Road,
Rockville, MD 20857 or e-mail a copy to
summer.king@samhsa.hhs.gov. Written
comments must be received before 60
days after the date of the publication in
the Federal Register.
Dated: July 21, 2011.
Kathleen G. Milenkowic,
Director, Division of Operational Support.
[FR Doc. 2011–18941 Filed 7–26–11; 8:45 am]
BILLING CODE 4162–20–P
DEPARTMENT OF HOMELAND
SECURITY
Federal Emergency Management
Agency
[Internal Agency Docket No. FEMA–1995–
DR; Docket ID FEMA–2011–0001]
sroberts on DSK5SPTVN1PROD with NOTICES
Vermont; Amendment No. 1 to Notice
of a Major Disaster Declaration
Federal Emergency
Management Agency, DHS.
ACTION: Notice.
AGENCY:
This notice amends the notice
of a major disaster declaration for the
State of Vermont (FEMA–1995–DR),
SUMMARY:
VerDate Mar<15>2010
17:08 Jul 26, 2011
Jkt 223001
dated June 15, 2011 and related
determinations.
DATES:
Effective Date: June 20, 2011.
FOR FURTHER INFORMATION CONTACT:
Peggy Miller, Office of Response and
Recovery, Federal Emergency
Management Agency, 500 C Street, SW.,
Washington, DC 20472, (202) 646–3886.
SUPPLEMENTARY INFORMATION: The notice
of a major disaster declaration for the
State of Vermont is hereby amended to
include the following area among those
areas determined to have been adversely
affected by the event declared a major
disaster by the President in his
declaration of June 15, 2011.
Washington County for Public Assistance.
The following Catalog of Federal Domestic
Assistance Numbers (CFDA) are to be used
for reporting and drawing funds: 97.030,
Community Disaster Loans; 97.031, Cora
Brown Fund; 97.032, Crisis Counseling;
97.033, Disaster Legal Services; 97.034,
Disaster Unemployment Assistance (DUA);
97.046, Fire Management Assistance Grant;
97.048, Disaster Housing Assistance to
Individuals and Households In Presidentially
Declared Disaster Areas; 97.049,
Presidentially Declared Disaster Assistance—
Disaster Housing Operations for Individuals
and Households; 97.050 Presidentially
Declared Disaster Assistance to Individuals
and Households—Other Needs; 97.036,
Disaster Grants—Public Assistance
PO 00000
Frm 00057
Fmt 4703
Sfmt 4703
(Presidentially Declared Disasters); 97.039,
Hazard Mitigation Grant.
Dated: June 23, 2011.
W. Craig Fugate,
Administrator, Federal Emergency
Management Agency.
[FR Doc. 2011–19030 Filed 7–26–11; 8:45 am]
BILLING CODE 9111–23–P
DEPARTMENT OF HOMELAND
SECURITY
Transportation Security Administration
Intent To Request Renewal From OMB
of One Current Public Collection of
Information: TSA Airspace Waiver
Program
Transportation Security
Administration, DHS.
ACTION: 60-day Notice.
AGENCY:
The Transportation Security
Administration (TSA) invites public
comment on one currently approved
Information Collection Request (ICR),
Office of Management and Budget
(OMB) control number 1652–0033,
abstracted below that we will submit to
OMB for renewal in compliance with
the Paperwork Reduction Act (PRA).
The ICR describes the nature of the
SUMMARY:
E:\FR\FM\27JYN1.SGM
27JYN1
Agencies
[Federal Register Volume 76, Number 144 (Wednesday, July 27, 2011)]
[Notices]
[Pages 44942-44944]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: 2011-18941]
-----------------------------------------------------------------------
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 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.
[[Page 44943]]
Cross-Site Evaluation of the Minority Substance Abuse/HIV Prevention
Program--(OMB No. 0930-0298)--Revision
The Substance Abuse and Mental Health Services Administration
(SAMHSA), Center for Substance Abuse Prevention (CSAP) is requesting
from the Office of Management and Budget (OMB) approval for the
revision of data collection activities for the cross-site study of the
Minority HIV/AIDS Initiative (MAI), which includes both youth and adult
questionnaires. This revision includes the addition of 4 cohorts,
changes to the data collection procedures based on intervention
duration, and the addition of two questions on binge drinking behavior.
The current approval is under OMB No. 0930-0298, which expires on 4/30/
12.
This cross-site evaluation supports two of SAMHSA's 8 Strategic
Initiatives: Prevention of Substance Abuse and Mental Illness and Data,
Outcomes, and Quality. It builds on six previous grant programs funded
by SAMHSA's CSAP to provide substance abuse and HIV prevention services
for minority populations. The first two were planning grant programs
and the last four were service grant programs. The goals for the Cohort
3-6 grants were to add, increase, or enhance integrated substance abuse
(SA) and HIV prevention services by providing supportive services and
strengthening linkages between service providers for at-risk minority
populations. The HIV Cohort 1-3 previously received clearance under OMB
No. 0930-0208 and Cohort 6 grants previously received clearance under
OMB No. 0930-0298. Since neither the HIV Cohort 4 nor the Cohort 5
Programs were cross-site studies, they did not require OMB clearance.
The current HIV Minority SA/HIV Prevention Program funded:
Cohorts 7 and 8 Prevention of Substance Abuse (SA) and HIV
for At-Risk Racial/Ethnic Minority Subpopulations Cooperative
Agreements--60 grants for 5 years,
Cohort 9 Ready-To-Respond Initiative--35 grants for 5
years, and
Cohort 10 Capacity Building Initiative--27 grants for 5
years.
Grantees are community based organizations that are required to
address the SAMSHA Strategic Prevention Framework (SPF) and participate
in this cross-site evaluation. The grantees are expected to provide
leadership and coordination on the planning and implementation of the
SPF that targets minority populations, the minority reentry population,
as well as other high risk groups residing in communities of color with
high prevalence of SA and HIV/AIDS. The primary objectives of the
cross-site study are to: (1) Determine the success of the MAI in
preventing, delaying, and/or reducing the use of alcohol, tobacco, and
other drugs (ATOD) among the target populations. The results of this
cross-site study will assist SAMHSA/CSAP in promoting and disseminating
optimally effective prevention programs; (2) Measure the effectiveness
of evidence-based programs and infrastructure development activities
such as: Outreach and training, mobilization of key stakeholders,
substance abuse and HIV/AIDS counseling and education, referrals to
appropriate medical treatment and/or other intervention strategies
(i.e., cultural enrichment activities, educational and vocational
resources, and computer-based curricula); and (3) Assess the process of
adopting and implementing the Strategic Prevention Framework (SPF) with
the target populations.
The grantees are expected to provide an effective prevention
process, direction, and a common set of goals, expectations, and
accountabilities to be adapted and integrated at the community level.
While the grantees have substantial flexibility in choosing their
individual evidence-based programs, they are all required to base them
on the five steps of the SPF to build service capacity specific to SA
and HIV prevention services. Conducting this cross-site evaluation will
assist SAMHSA/CSAP in promoting and disseminating optimally effective
prevention programs.
Grantees must also conduct ongoing monitoring and evaluation of
their projects to assess program effectiveness including Federal
reporting of the Government Performance and Results Act (GPRA) of 1993,
SAMHSA/CSAP National Outcome Measures (NOMs), and HIV Counseling and
Testing. All of this information will be collected through self-report
questionnaires administered to program participants. All grantees will
use two instruments, one for youth aged between 12 and 17 and one for
adults aged 18 and older. Participants in interventions lasting 30 days
or longer will complete questionnaires three times, taking an average
of 50 minutes for baseline, exit, and follow-up questionnaires.
Participants in interventions lasting 2-29 days will complete
questionnaires two times taking an average of 30 minutes to complete.
Single-session intervention participants will complete one
questionnaire at exit only. The GPRA and NOMs measures on the
instruments have already been approved by OMB (OMB No. 0930-0230), and
the remaining HIV-related questions have been approved under OMB No.
0930-0298.The youth questionnaire contains 125 questions, of which 28
relate to HIV/AIDS and the adult questionnaire contains 118 items, 47
of which relate to HIV/AIDS. Two additional questions have been added
to address SAMHSA's need to collect information on binge drinking
behavior.
These questions are:
1. Females only: During the past 30 days, on how many days did you
have 4 or more drinks on the same occasion?
2. Males only: During the past 30 days, on how many days did you
have 5 or more drinks on the same occasion?
Sample size, respondent burden, and intrusiveness have been
minimized to be consistent with the cross-site objectives. Procedures
are employed to safeguard the privacy and confidentiality of
participants. Every effort has been made to coordinate cross-site data
collection with local data collection efforts in an attempt to minimize
respondent burden.
The cross-site evaluation results will have significant
implications for the substance abuse and HIV/AIDS prevention fields,
the allocation of grant funds, and other evaluation activities
conducted by multiple Federal, State, and local government agencies.
They will be used to develop Federal policy in support of SAMHSA/CSAP
program initiatives, inform the public of lessons learned and findings,
improve existing programs, and promote replication and dissemination of
effective prevention strategies.
Total Estimates of Annualized Hour Burden
The following table shows the estimated annualized burden for data
collection.
[[Page 44944]]
Table 1a--Estimates of Annualized Hour Burden by Intervention Length
----------------------------------------------------------------------------------------------------------------
Number of Responses per Total Hours per Total hour
Intervention length respondents respondent responses response burden
----------------------------------------------------------------------------------------------------------------
30-Day or More Intervention
----------------------------------------------------------------------------------------------------------------
Baseline........................ 7,937 1 7,937 0.83 6,588
Exit............................ 4,887 1 4,887 0.83 4,056
Follow-up....................... 2,942 1 2,942 0.83 2,442
-------------------------------------------------------------------------------
Subtotal.................... 7,937 .............. 15,766 .............. 13,086
----------------------------------------------------------------------------------------------------------------
2- to 29-Day Intervention
----------------------------------------------------------------------------------------------------------------
Baseline........................ 1,416 1 1,416 0.5 708
Exit............................ 872 1 872 0.5 436
-------------------------------------------------------------------------------
Subtotal.................... 1,416 .............. 2,288 .............. 1,144
----------------------------------------------------------------------------------------------------------------
Single Day Intervention
----------------------------------------------------------------------------------------------------------------
Exit............................ 2,458 1 2,458 0.25 614
-------------------------------------------------------------------------------
Annualized Total............ 11,811 .............. 20,512 .............. 14,844
----------------------------------------------------------------------------------------------------------------
Table 1b--Estimates of Annualized Hour Burden by Survey Type
----------------------------------------------------------------------------------------------------------------
Number of Total Total hour
Questionnaire respondents responses burden
----------------------------------------------------------------------------------------------------------------
Annualized Total Adult.......................................... 9,682 16,899 12,234
Annualized Total Youth.......................................... 2,128 3,612 2,610
-----------------------------------------------
Annualized Total............................................ 11,811 20,512 14,844
----------------------------------------------------------------------------------------------------------------
Send comments to Summer King, SAMHSA Reports Clearance Officer,
Room 8-1099, One Choke Cherry Road, Rockville, MD 20857 or e-mail a
copy to summer.king@samhsa.hhs.gov. Written comments must be received
before 60 days after the date of the publication in the Federal
Register.
Dated: July 21, 2011.
Kathleen G. Milenkowic,
Director, Division of Operational Support.
[FR Doc. 2011-18941 Filed 7-26-11; 8:45 am]
BILLING CODE 4162-20-P