Proposed Data Collections Submitted for Public Comment and Recommendations, 49520-49521 [2014-19826]
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49520
Federal Register / Vol. 79, No. 162 / Thursday, August 21, 2014 / Notices
sample size of 528. The baseline and
follow up questionnaires contain
questions about participants’ socio-
demographic information, health and
healthcare, sexual activity, substance
use, and other psychosocial issues.
There is no cost to participants other
than their time.
ESTIMATED ANNUALIZED BURDEN HOURS
Number
responses per
respondent
Number of
respondents
Average
burden per
respondent
(in hours)
Total
annual
burden
(in hours)
Type of respondent
Form name
Prospective Participant .....................
160
1
5/60
13
160
80
80
1
1
1
5/60
10/60
10/60
13
13
13
80
40
100
170
10
1
3
1
1
1
1
5/60
1
1
10/60
80
10
100
170
2
Enrolled Participant ...........................
Outreach Recruitment Assessment
(screener).
Limited Locator Form .......................
RCT Informed Consent Form ..........
Participant
Contact
Information
Form.
Baseline Questionnaire ....................
Client Satisfaction Survey ................
3-month follow up Questionnaire .....
6-month follow up Questionnaire .....
Success Case Study Informed Consent Form.
Success Case Study Interview ........
10
1
1.5
15
Total ...........................................
...........................................................
........................
........................
........................
429
Prospective Participant .....................
Enrolled Participant ...........................
Enrolled Participant ...........................
Enrolled
Enrolled
Enrolled
Enrolled
Enrolled
Participant
Participant
Participant
Participant
Participant
...........................
...........................
...........................
...........................
...........................
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. 2014–19827 Filed 8–20–14; 8:45 am]
BILLING CODE 4163–18–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Disease Control and
Prevention
[60-Day–14–0278]
mstockstill on DSK4VPTVN1PROD 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
VerDate Mar<15>2010
17:18 Aug 20, 2014
Jkt 232001
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
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
National Hospital Ambulatory
Medical Care Survey (NHAMCS) (OMB
Control No. 0920–0278, expires 12/31/
2014)—Revision—National Center for
PO 00000
Frm 00030
Fmt 4703
Sfmt 4703
Health Statistics (NCHS), Centers for
Disease Control and Prevention (CDC).
Background and Brief Description
Section 306 of the Public Health
Service (PHS) Act (42 U.S.C. 242k), as
amended, authorizes that the Secretary
of Health and Human Services (DHHS),
acting through NCHS, shall collect
statistics on ‘‘utilization of health care’’
in the United States. The National
Hospital Ambulatory Medical Care
Survey (NHAMCS) has been conducted
annually since 1992. NCHS is seeking
OMB approval to extend this survey for
an additional three years and make
minor modifications to survey
questionnaires.
The purpose of NHAMCS is to meet
the needs and demands for statistical
information about the provision of
ambulatory medical care services in the
United States. Ambulatory services are
rendered in a wide variety of settings,
including physicians’ offices and
hospital outpatient and emergency
departments. The target universe of the
NHAMCS is in-person visits made to
outpatient departments (OPDs),
emergency departments (EDs), and
ambulatory surgery locations (ASLs) of
non-Federal, short-stay hospitals
(hospitals with an average length of stay
of less than 30 days) or those whose
specialty is general (medical or surgical)
or children’s general.
NHAMCS was initiated to
complement the National Ambulatory
Medical Care Survey (NAMCS, OMB
No. 0920–0234), which provides similar
data concerning patient visits to
physicians’ offices. NAMCS and
NHAMCS are the principal sources of
E:\FR\FM\21AUN1.SGM
21AUN1
49521
Federal Register / Vol. 79, No. 162 / Thursday, August 21, 2014 / Notices
data on ambulatory care provided in the
United States.
NHAMCS provides a range of baseline
data on the characteristics of the users
and providers of hospital ambulatory
medical care. Data collected include
patients’ demographic characteristics,
reason(s) for visit, providers’ diagnoses,
diagnostic services, medications, and
disposition. These data, together with
trend data, may be used to monitor the
effects of change in the health care
system, for the planning of health
services, improving medical education,
determining health care work force
needs, and assessing the health status of
the population.
Users of NHAMCS data include, but
are not limited to, congressional offices,
Federal agencies, state and local
governments, schools of public health,
colleges and universities, private
industry, nonprofit foundations,
professional associations, clinicians,
researchers, administrators, and health
planners. There are no costs to the
respondents other than their time.
ESTIMATED ANNUALIZED BURDEN HOURS
Number of
responses per
respondent
Number of
respondents
Average
burden per
response
(in hours)
Total
burden
hours
Type of respondent
Form name
Hospital Chief Executive Officer .......
Ancillary Service Executive ...............
Physician/Registered Nurse/Medical
Record Clerk.
Physician/Registered Nurse/Medical
Record Clerk.
Physician/Registered Nurse/Medical
Record Clerk.
Medical Record Clerk ........................
Hospital Induction ............................
Ambulatory Unit Induction ...............
ED Patient Record form ..................
458
1,750
33
1
1
100
1.5
15/60
7/60
687
438
385
OPD Patient Record form ................
23
200
14/60
1,073
AS Patient Record Form .................
23
100
7/60
268
Retrieving Patient Records (ED,
OPD, and AS).
Reabstraction Telephone Call .........
696
133
1/60
1,543
72
1
5/60
6
Pulling and re-filing Patient Records
(ED, OPD, and AS).
72
10
1/60
12
..........................................................
........................
........................
........................
4,412
Ancillary Service Executive—Reabstraction.
Medical Record Clerk—Reabstraction.
Total ...........................................
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. 2014–19826 Filed 8–20–14; 8:45 am]
BILLING CODE 4163–18–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Administration for Children and
Families
Proposed Information Collection
Activity; Comment Request
Title: Job Search Assistance (JSA)
Strategies Evaluation.
OMB No.: 0970–0440.
Description: The Administration for
Children and Families (ACF) is
proposing a data collection activity as
part of the Job Search Assistance (JSA)
Strategies Evaluation. The JSA
evaluation will aim to determine which
JSA strategies are most effective in
moving TANF applicants and recipients
into work. The impact study will
randomly assign individuals to
contrasting JSA approaches and then
compare their employment and earnings
to determine their relative effectiveness.
The implementation study will describe
services participants receive under each
approach as well as provide operational
lessons gathered directly from
practitioners.
The proposed information collection
activity consists of: (1) Baseline data
collection: Collection of baseline data
from TANF recipients at the time of
enrollment in the study; (2)
Implementation study site visits:
Conducting site visits for the purpose of
documenting the program context,
program organization and staffing, the
components JSA services, and other
relevant aspects of the TANF program.
During the visits, site teams will
interview key administrators and line
staff using a semi-structured interview
guide; and (3) a JSA staff survey. This
on-line survey, administered to TANF
supervisory and line staff involved in
JSA activities, will be used as part of the
implementation study to systematically
document program operations and the
type of JSA services provided across the
study sites.
Respondents: JSA program staff and
individuals enrolled in the JSA study.
ANNUAL BURDEN ESTIMATES
Total
number of
respondents
mstockstill on DSK4VPTVN1PROD with NOTICES
Instrument
Baseline information form ..................................................
JSA staff Survey ................................................................
Implementation study site visits .........................................
VerDate Mar<15>2010
17:18 Aug 20, 2014
Jkt 232001
PO 00000
Frm 00031
Annual
number of
respondents
25,000
660
300
Fmt 4703
Sfmt 4703
Number of
responses per
respondent
8,333
220
100
E:\FR\FM\21AUN1.SGM
1
1
1
21AUN1
Average
burden
hours per
response
Total
annual
burden
hours
0.2
0.5
1
1667
110
100
Agencies
[Federal Register Volume 79, Number 162 (Thursday, August 21, 2014)]
[Notices]
[Pages 49520-49521]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: 2014-19826]
-----------------------------------------------------------------------
DEPARTMENT OF HEALTH AND HUMAN SERVICES
Centers for Disease Control and Prevention
[60-Day-14-0278]
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 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
National Hospital Ambulatory Medical Care Survey (NHAMCS) (OMB
Control No. 0920-0278, expires 12/31/2014)--Revision--National Center
for Health Statistics (NCHS), Centers for Disease Control and
Prevention (CDC).
Background and Brief Description
Section 306 of the Public Health Service (PHS) Act (42 U.S.C.
242k), as amended, authorizes that the Secretary of Health and Human
Services (DHHS), acting through NCHS, shall collect statistics on
``utilization of health care'' in the United States. The National
Hospital Ambulatory Medical Care Survey (NHAMCS) has been conducted
annually since 1992. NCHS is seeking OMB approval to extend this survey
for an additional three years and make minor modifications to survey
questionnaires.
The purpose of NHAMCS is to meet the needs and demands for
statistical information about the provision of ambulatory medical care
services in the United States. Ambulatory services are rendered in a
wide variety of settings, including physicians' offices and hospital
outpatient and emergency departments. The target universe of the NHAMCS
is in-person visits made to outpatient departments (OPDs), emergency
departments (EDs), and ambulatory surgery locations (ASLs) of non-
Federal, short-stay hospitals (hospitals with an average length of stay
of less than 30 days) or those whose specialty is general (medical or
surgical) or children's general.
NHAMCS was initiated to complement the National Ambulatory Medical
Care Survey (NAMCS, OMB No. 0920-0234), which provides similar data
concerning patient visits to physicians' offices. NAMCS and NHAMCS are
the principal sources of
[[Page 49521]]
data on ambulatory care provided in the United States.
NHAMCS provides a range of baseline data on the characteristics of
the users and providers of hospital ambulatory medical care. Data
collected include patients' demographic characteristics, reason(s) for
visit, providers' diagnoses, diagnostic services, medications, and
disposition. These data, together with trend data, may be used to
monitor the effects of change in the health care system, for the
planning of health services, improving medical education, determining
health care work force needs, and assessing the health status of the
population.
Users of NHAMCS data include, but are not limited to, congressional
offices, Federal agencies, state and local governments, schools of
public health, colleges and universities, private industry, nonprofit
foundations, professional associations, clinicians, researchers,
administrators, and health planners. There are no costs to the
respondents other than their time.
Estimated Annualized Burden Hours
--------------------------------------------------------------------------------------------------------------------------------------------------------
Number of Average burden
Type of respondent Form name Number of responses per per response Total burden
respondents respondent (in hours) hours
--------------------------------------------------------------------------------------------------------------------------------------------------------
Hospital Chief Executive Officer............... Hospital Induction..................... 458 1 1.5 687
Ancillary Service Executive.................... Ambulatory Unit Induction.............. 1,750 1 15/60 438
Physician/Registered Nurse/Medical Record Clerk ED Patient Record form................. 33 100 7/60 385
Physician/Registered Nurse/Medical Record Clerk OPD Patient Record form................ 23 200 14/60 1,073
Physician/Registered Nurse/Medical Record Clerk AS Patient Record Form................. 23 100 7/60 268
Medical Record Clerk........................... Retrieving Patient Records (ED, OPD, 696 133 1/60 1,543
and AS).
Ancillary Service Executive--Reabstraction..... Reabstraction Telephone Call........... 72 1 5/60 6
Medical Record Clerk--Reabstraction............ Pulling and re-filing Patient Records 72 10 1/60 12
(ED, OPD, and AS).
---------------------------------------------------------------
Total...................................... ....................................... .............. .............. .............. 4,412
--------------------------------------------------------------------------------------------------------------------------------------------------------
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. 2014-19826 Filed 8-20-14; 8:45 am]
BILLING CODE 4163-18-P