Agency Information Collection Activities: Submission for OMB Review; Comment Request, 63931-63932 [2011-26590]
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Federal Register / Vol. 76, No. 199 / Friday, October 14, 2011 / Notices
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Health Resources and Services
Administration
Agency Information Collection
Activities: Submission for OMB
Review; Comment Request
Periodically, the Health Resources
and Services Administration (HRSA)
publishes abstracts of information
collection requests under review by the
Office of Management and Budget
(OMB), in compliance with the
Paperwork Reduction Act of 1995 (44
U.S.C. chapter 35). To request a copy of
the clearance requests submitted to
OMB for review, e-mail
paperwork@hrsa.gov or call the HRSA
Reports Clearance Office at (301) 443–
1129.
The following request has been
submitted to the Office of Management
and Budget for review under the
Paperwork Reduction Act of 1995:
Proposed Project Title: Evaluation of
the Text4baby Program—(OMB No.
0915–xxxx)—[NEW]
Background: Text4baby is a mobile
health education program that provides
free, brief, evidence-based, health
messages to women who are pregnant or
have an infant under one year of age. An
educational program led by the National
Healthy Mothers, Healthy Babies
coalition (HMHB), Text4baby is
Instrument
Consent Training and Coordination.
Prenatal Patient Consent ....
Parent-of-Minor Consent .....
intended to help women have safe and
healthy pregnancies by empowering
them with information they need to give
their babies the best possible start in
life. The Text4baby program was
launched nationally in February 2010.
Text4baby is made possible through a
broad, public-private partnership that
includes government and Tribal
agencies, corporations, academic
institutions, professional associations,
and non-profit organizations.
The goal of this program evaluation is
to examine the characteristics of women
who utilize the Text4baby mobile
phone-based program, to assess their
experience with the program, and to
determine whether enrollment in
Text4baby is associated with healthy
behaviors and timely access to health
care during pregnancy and an infant’s
first year of life.
This information will help the
Department of Health and Human
Services understand the usefulness of
mobile health technology and the
potential for expanding and/or adapting
mobile phone messaging to additional
health topics or conditions. The study
also may offer insight into planning and
implementing similar projects.
Purpose: The purpose of the
evaluation is to assess the usefulness of
the Text4baby program.
The four data collection components
are as follows:
• Safety Consumer Net Survey with
subscribers and non-subscribers to the
Text4baby program who receive
Responses
per
respondent
Number of
respondents
Person incurring burden
prenatal care in community health
centers in four communities. The health
centers will recruit eligible women,
obtain their signed consent to
participate in the study, and convey
their contact information to the data
collection contractor. Data from the
telephone survey will be linked to
selected data from electronic health
records (EHRs) for respondents who
consent to the release of their EHRs. The
survey will be conducted in two rounds:
Round 1 will include pregnant women
and Round 2 will include the same
women approximately nine months
later during the postpartum period.
• Focus Groups with current
subscribers in four communities to
obtain more in-depth qualitative data
regarding the usefulness of the messages
and the program.
• Key Informant Interviews of a
diverse mix of providers in four
communities to obtain provider
perspectives on the usefulness of the
Text4baby programs. Providers could
include physicians, midwives, nurses,
case managers, outreach workers, and
health educators.
• Stakeholder Interviews with
Text4baby partners (public and private)
to examine the implementation of
Text4baby at the national, regional,
state, or local level, including outreach,
enrollment, coalition building,
sustainability, and replication.
The annual estimate of burden is as
follows:
Total
responses
Hours per
response
Total burden
hours
Health Center Study Coordinators.
Health Center Staff ............
Health Center Staff ............
Prenatal Patient ..................
Health Center Staff ............
Parent of Minor ..................
Prenatal Patient ..................
8
12
96
1.00
96
32
1630
1630
195
195
960
1
1
1
1
1
1
32
1630
1630
195
195
960
1.00
0.08
0.08
0.25
0.08
0.33
32
130
130
49
16
317
Postpartum Patient .............
768
1
768
0.33
253
Prenatal/Postpartum Patient
Providers ............................
Stakeholders ......................
80
40
30
1
1
1
80
40
30
1.50
0.75
0.75
120
30
23
Total .............................
tkelley on DSK3SPTVN1PROD with NOTICES
Safety Net Consumer Survey Round 1.
Safety Net Consumer Survey Round 2.
Focus Groups .....................
Key Informant Interviews ....
Stakeholder Interviews ........
.............................................
........................
........................
........................
........................
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63932
Federal Register / Vol. 76, No. 199 / Friday, October 14, 2011 / Notices
Written comments and
recommendations concerning the
proposed information collection should
be sent within 30 days of this notice to
the desk officer for HRSA, either by email to OIRA_submission@omb.eop.gov
or by fax to 202–395–6974. Please direct
all correspondence to the ‘‘attention of
the desk officer for HRSA.’’
Dated: October 7, 2011.
Reva Harris,
Acting Director, Division of Policy and
Information Coordination.
[FR Doc. 2011–26590 Filed 10–13–11; 8:45 am]
BILLING CODE 4165–15–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
National Institutes of Health
National Human Genome Research
Institute; 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.
tkelley on DSK3SPTVN1PROD with NOTICES
Name of Committee: National Human
Genome Research Institute Special Emphasis
Panel, ENCODE Technology RFA–SEP.
Date: November 29, 2011.
Time: 8 a.m. to 5 p.m.
Agenda: To review and evaluate grant
applications.
Place: Residence Inn Bethesda, 7335
Wisconsin Avenue, Bethesda, MD 20814.
Contact Person: Keith McKenney, PhD,
Scientific Review Officer, NHGRI, 5635
Fishers Lane, Suite 4076, Bethesda, MD
20814, 301–594–4280,
mckenneyk@mail.nih.gov.
(Catalogue of Federal Domestic Assistance
Program Nos. 93.172, Human Genome
Research, National Institutes of Health, HHS)
Dated: October 7, 2011 .
Jennifer S. Spaeth,
Director, Office of Federal Advisory
Committee Policy.
[FR Doc. 2011–26617 Filed 10–13–11; 8:45 am]
BILLING CODE 4140–01–P
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15:20 Oct 13, 2011
Jkt 226001
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
National Institutes of Health
National Institute of Diabetes and
Digestive and Kidney Diseases; Notice
of Closed Meetings
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: National Institute of
Diabetes and Digestive and Kidney Diseases
Special Emphasis Panel, NIDDK Ancillary
RO1 Telephone Review SEP.
Date: November 14, 2011.
Time: 1 p.m. to 2:30 p.m.
Agenda: To review and evaluate grant
applications.
Place: National Institutes of Health, Two
Democracy Plaza, 6707 Democracy
Boulevard, Bethesda, MD 20892, (Telephone
Conference Call).
Contact Person: Xiaodu Guo, M.D., PhD,
Scientific Review Officer, Review Branch,
DEA, NIDDK, National Institutes of Health,
Room 761, 6707 Democracy Boulevard,
Bethesda, MD 20892–5452, (301) 594–4719,
guox@extra.niddk.nih.gov.
Name of Committee: National Institute of
Diabetes and Digestive and Kidney Diseases
Special Emphasis Panel, NIDDK PO1
Telephone Review SEP.
Date: November 29, 2011.
Time: 1 p.m. to 3 p.m.
Agenda: To review and evaluate grant
applications.
Place: National Institutes of Health, Two
Democracy Plaza, 6707 Democracy
Boulevard, Bethesda, MD 20892, (Telephone
Conference Call).
Contact Person: Xiaodu Guo, M.D., PhD,
Scientific Review Officer, Review Branch,
DEA, NIDDK, National Institutes of Health,
Room 761, 6707 Democracy Boulevard,
Bethesda, MD 20892–5452, (301) 594–4719,
guox@extra.niddk.nih.gov.
(Catalogue of Federal Domestic Assistance
Program Nos. 93.847, Diabetes,
Endocrinology and Metabolic Research;
93.848, Digestive Diseases and Nutrition
Research; 93.849, Kidney Diseases, Urology
and Hematology Research, National Institutes
of Health, HHS)
PO 00000
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Fmt 4703
Sfmt 4703
Dated: October 7, 2011.
Jennifer S. Spaeth,
Director, Office of Federal Advisory
Committee Policy.
[FR Doc. 2011–26620 Filed 10–13–11; 8:45 am]
BILLING CODE 4140–01–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
National Institutes of Health
Eunice Kennedy Shriver National
Institute of Child Health & Human
Development; Notice of Meeting
Pursuant to section 10(d) of the
Federal Advisory Committee Act, as
amended (5 U.S.C. App.), notice is
hereby given of a meeting of the Board
of Scientific Counselors, NICHD.
The meeting will be open to the
public as indicated below, with the
attendance limited to space available.
Individuals who plan to attend and
need special assistance, such as sign
language interpretation or other
reasonable accommodations, should
notify the Contact Person listed below
in advance of the meeting.
The meeting will be closed to the
public as indicated below in accordance
with the provisions set forth in section
552b(c)(6), Title 5 U.S.C., as amended
for the review, discussion, and
evaluation of individual intramural
programs and projects conducted by the
Eunice Kennedy Shriver National
Institute of Child Health & Human
Development, including consideration
of personnel qualifications and
performance, and the competence of
individual investigators, the disclosure
of which would constitute a clearly
unwarranted invasion of personal
privacy.
Name of Committee: Board of Scientific
Counselors, NICHD.
Date: December 2, 2011.
Open: 8 a.m. to 11:30 a.m.
Agenda: A report by the Scientific Director,
NICHD, on the status of the NICHD Division
of Intramural Research.
Place: National Institutes of Health,
Building 31, 9000 Rockville Pike, Room
2A48, Bethesda, MD 20892.
Closed: 11:30 a.m. to 4 p.m.
Agenda: To review and evaluate personal
qualifications and performance, and
competence of individual investigators.
Place: National Institutes of Health,
Building 31, 9000 Rockville Pike, Room
2A48, Bethesda, MD 20892.
Contact Person: Constantine A. Stratakis,
MD, D(med)Sci, Scientific Director, Eunice
Kennedy Shriver National Institute of Child
Health and Human Development, NIH, 9000
Rockville Pike, Building 31, Room 2A46,
Bethesda, MD 20892, 301–594–5984,
stratakc@mail.nih.gov.
E:\FR\FM\14OCN1.SGM
14OCN1
]]>Agencies
[Federal Register Volume 76, Number 199 (Friday, October 14, 2011)]
[Notices]
[Pages 63931-63932]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: 2011-26590]
[[Page 63931]]
-----------------------------------------------------------------------
DEPARTMENT OF HEALTH AND HUMAN SERVICES
Health Resources and Services Administration
Agency Information Collection Activities: Submission for OMB
Review; Comment Request
Periodically, the Health Resources and Services Administration
(HRSA) publishes abstracts of information collection requests under
review by the Office of Management and Budget (OMB), in compliance with
the Paperwork Reduction Act of 1995 (44 U.S.C. chapter 35). To request
a copy of the clearance requests submitted to OMB for review, e-mail
paperwork@hrsa.gov or call the HRSA Reports Clearance Office at (301)
443-1129.
The following request has been submitted to the Office of
Management and Budget for review under the Paperwork Reduction Act of
1995:
Proposed Project Title: Evaluation of the Text4baby Program--(OMB No.
0915-xxxx)--[NEW]
Background: Text4baby is a mobile health education program that
provides free, brief, evidence-based, health messages to women who are
pregnant or have an infant under one year of age. An educational
program led by the National Healthy Mothers, Healthy Babies coalition
(HMHB), Text4baby is intended to help women have safe and healthy
pregnancies by empowering them with information they need to give their
babies the best possible start in life. The Text4baby program was
launched nationally in February 2010. Text4baby is made possible
through a broad, public-private partnership that includes government
and Tribal agencies, corporations, academic institutions, professional
associations, and non-profit organizations.
The goal of this program evaluation is to examine the
characteristics of women who utilize the Text4baby mobile phone-based
program, to assess their experience with the program, and to determine
whether enrollment in Text4baby is associated with healthy behaviors
and timely access to health care during pregnancy and an infant's first
year of life.
This information will help the Department of Health and Human
Services understand the usefulness of mobile health technology and the
potential for expanding and/or adapting mobile phone messaging to
additional health topics or conditions. The study also may offer
insight into planning and implementing similar projects.
Purpose: The purpose of the evaluation is to assess the usefulness
of the Text4baby program.
The four data collection components are as follows:
Safety Consumer Net Survey with subscribers and non-
subscribers to the Text4baby program who receive prenatal care in
community health centers in four communities. The health centers will
recruit eligible women, obtain their signed consent to participate in
the study, and convey their contact information to the data collection
contractor. Data from the telephone survey will be linked to selected
data from electronic health records (EHRs) for respondents who consent
to the release of their EHRs. The survey will be conducted in two
rounds: Round 1 will include pregnant women and Round 2 will include
the same women approximately nine months later during the postpartum
period.
Focus Groups with current subscribers in four communities
to obtain more in-depth qualitative data regarding the usefulness of
the messages and the program.
Key Informant Interviews of a diverse mix of providers in
four communities to obtain provider perspectives on the usefulness of
the Text4baby programs. Providers could include physicians, midwives,
nurses, case managers, outreach workers, and health educators.
Stakeholder Interviews with Text4baby partners (public and
private) to examine the implementation of Text4baby at the national,
regional, state, or local level, including outreach, enrollment,
coalition building, sustainability, and replication.
The annual estimate of burden is as follows:
--------------------------------------------------------------------------------------------------------------------------------------------------------
Number of Responses per Total Hours per Total burden
Instrument Person incurring burden respondents respondent responses response hours
--------------------------------------------------------------------------------------------------------------------------------------------------------
Consent Training and Coordination......... Health Center Study 8 12 96 1.00 96
Coordinators.
Health Center Staff......... 32 1 32 1.00 32
Prenatal Patient Consent.................. Health Center Staff......... 1630 1 1630 0.08 130
Prenatal Patient............ 1630 1 1630 0.08 130
Parent-of-Minor Consent................... Health Center Staff......... 195 1 195 0.25 49
Parent of Minor............. 195 1 195 0.08 16
Safety Net Consumer Survey Round 1........ Prenatal Patient............ 960 1 960 0.33 317
Safety Net Consumer Survey Round 2........ Postpartum Patient.......... 768 1 768 0.33 253
Focus Groups.............................. Prenatal/Postpartum Patient. 80 1 80 1.50 120
Key Informant Interviews.................. Providers................... 40 1 40 0.75 30
Stakeholder Interviews.................... Stakeholders................ 30 1 30 0.75 23
-------------------------------------------------------------------------------------------------------------
Total................................. ............................ .............. .............. .............. .............. 1196
--------------------------------------------------------------------------------------------------------------------------------------------------------
[[Page 63932]]
Written comments and recommendations concerning the proposed
information collection should be sent within 30 days of this notice to
the desk officer for HRSA, either by e-mail to OIRA_submission@omb.eop.gov or by fax to 202-395-6974. Please direct all
correspondence to the ``attention of the desk officer for HRSA.''
Dated: October 7, 2011.
Reva Harris,
Acting Director, Division of Policy and Information Coordination.
[FR Doc. 2011-26590 Filed 10-13-11; 8:45 am]
BILLING CODE 4165-15-P
