Agency Information Collection Activities: Proposed Collection; Comment Request, 20920-20922 [05-7988]
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20920
Federal Register / Vol. 70, No. 77 / Friday, April 22, 2005 / Notices
designated HPSA approved by the
Secretary for LRP participants.
This request for extension of OMB
approval will include the NHSC LRP
Application, Loan Verification Form,
Site Information Form, Request for
Method of Advanced Loan Repayment
Number of
respondents
Type of respondents
Form and Authorization to Release
Information Form.
The estimate of burden is as follows:
Responses
per
respondent
*1
Total
responses
Hours per
responses
Total burden hours
Applicants ..............................................................................................
Lenders ..................................................................................................
1430
70
**1
1430
70
1.5
.25
2145
18
Total ................................................................................................
1500
....................
1500
......................
2163
*An
applicant response includes completion of one of each of the above-listed forms, and may include the completion of additional Loan
Verification Forms (one for each educational loan for which he or she is seeking repayment).
**A lender response includes completion of one Loan Verification Form for each educational loan of an applicant it holds.
Written comments and
recommendations concerning the
proposed information collection should
be sent within 30 days of this notice to:
John Kraemer, Desk Officer, Human
Resources and Housing Branch, Office
of Management and Budget, New
Executive Office Building, Room 10235,
Washington, DC 20503.
Dated: April 18, 2005.
Tina M. Cheatham,
Director, Division of Policy Review and
Coordination.
[FR Doc. 05–8106 Filed 4–21–05; 8:45 am]
BILLING CODE 4165–15–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
National Advisory Council on Migrant
Health; Notice of Meeting
In accordance with section 10(a)(2) of
the Federal Advisory Committee Act
(Pub. L. 92–463), notice is hereby given
of the following meeting:
Name: National Advisory Council on
Migrant Health.
Dates and Times: May 11, 2005, 9 a.m. to
5 p.m., May 12, 2005, 9 a.m. to 5 p.m.
Place: Caribe Hilton Hotel, San Geronimo
Grounds, Los Rosales Street, San Juan, Puerto
Rico 00901, Phone: (787) 721–0303; Fax:
(787) 722–2910.
Status: The meeting will be open to the
public.
Agenda: The agenda includes an overview
of the Council’s general business activities.
The Council will also develop
recommendations to the Secretary of Health
and Human Services. Finally, the Council
will hear presentations from experts on
farmworker issues, including the status of
farmworker health at the local and national
level.
The Council meeting is being held in
conjunction with the National Farmworker
Health Conference sponsored by the National
Association of Community Health Centers,
Inc., the Migrant Clinicians Network, and the
15:27 Apr 21, 2005
Jkt 205001
Dated: April 18, 2005.
Tina M. Cheatham,
Director, Division of Policy Review and
Coordination.
[FR Doc. 05–8104 Filed 4–21–05; 8:45 am]
BILLING CODE 4165–15–P
Health Resources and Services
Administration
VerDate jul<14>2003
National Center for Farmworker Health,
which is being held in San Juan, Puerto Rico,
during the same period of time.
Agenda items are subject to change as
priorities indicate.
For Further Information Contact: Anyone
requiring information regarding the Council
should contact Gladys Cate, Office of
Minority and Special Populations, staff
support to the National Advisory Council on
Migrant Health, Bureau of Primary Health
Care, Health Resources and Services
Administration, 5600 Fishers Lane,
Rockville, Maryland 20857, Telephone (301)
594–0367.
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 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
PO 00000
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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: Cross-Site Evaluation
of the National Child Traumatic Stress
Initiative (NCTSI)—NEW
The Substance Abuse and Mental
Health Services Administration’s
(SAMHSA), Center for Mental Health
Services (CMHS) will conduct the
Cross-Site Evaluation of the National
Child Traumatic Stress Initiative
(NCTSI). The data collected will
describe the children and families
served by the National Child Traumatic
Stress Network (NCTSN) and their
outcomes, assess the development and
dissemination of effective treatments
and services, evaluate intra-network
collaboration, and assess the Network’s
impact beyond the NCTSN.
Data will be collected from caregivers,
NCTSN staff (e.g., project directors,
researchers, and providers), mental
health providers outside of the NCTSN,
and non-mental health service providers
who provide services to children
outside of the NCTSN. Data collection
will take place in 31 Community
Treatment and Services Programs (CTS),
13 Treatment and Service Adaptation
Centers (TSA), and 2 National Centers
for Child Traumatic Stress (NCCTS).
Data collection for this evaluation will
be conducted over a four-year period.
In order to describe the children
served, their outcomes, and satisfaction
with services, data will be collected
from youth ages 7–18 who are receiving
services in the NCTSN, and from
caregivers for all children who are
receiving NCTSN services. Data will be
collected when the child/youth enters
services and during subsequent followup sessions at three-month intervals
over the course of one year.
E:\FR\FM\22APN1.SGM
22APN1
20921
Federal Register / Vol. 70, No. 77 / Friday, April 22, 2005 / Notices
Approximately 2,121 youth and 3,000
caregivers will participate in the
evaluation.
Data will be collected for use in the
development of evaluation measures
that will assess the development,
dissemination and adoption of traumainformed services. These data will be
collected from a total of approximately
110 NCTSN service providers, project
directors and NCCTS staff. Data will be
collected one time from these
respondents.
Measures that collect data on
development, dissemination, and
adoption of trauma-informed services
and other NCTSN products will be
administered to approximately 1,100
service providers, 44 project directors,
and 44 researchers/evaluators. These
measures will be administered once per
year in each of the four years of the
evaluation.
To assess collaboration across the
network, data will be collected from
approximately 450 NCTSI staff and 44
project directors/principal investigators.
The surveys associated with this data
collection will be administered at
varying intervals, with either one or two
data collection points per respondent
over the four years of the evaluation.
Number of
respondents
Instrument
Caregivers:
Child Behavior Checklist 1.5–5/6–18 .......................................................
Service Summary Form ............................................................................
Baseline/Renewal Assessment ................................................................
Core Clinical Characteristics Form ...........................................................
Youth Services Survey for Families .........................................................
Case Study Interviews ..............................................................................
Youth:
Trauma Symptoms Checklist for Children-Abbreviated ...........................
UCLA-PTSD short form ............................................................................
Network Service Provider:
Key Informant Interviews ..........................................................................
Focus Groups ...........................................................................................
Trauma-informed Service Provider Survey ..............................................
General Adoption Assessment Survey .....................................................
Adoption and Implementation Factors Interview ......................................
Project Director/Principal Investigator:
Key Informant Interviews ..........................................................................
Focus Groups ...........................................................................................
Trauma-informed Service Provider Survey ..............................................
Product/Innovations Development and Dissemination Survey ................
General Adoption Assessment Survey .....................................................
Adoption and Implementation Factors Interview ......................................
Network Survey ........................................................................................
Other Network Staff:
Key Informant Interviews ..........................................................................
Trauma-informed Service Provider Survey ..............................................
Telephone Interviews ...............................................................................
Case study interviews ..............................................................................
General Adoption Assessment Survey .....................................................
Adoption and Implementation Factors Interview ......................................
Network Survey ........................................................................................
Partner Participatory Assessment Tool ....................................................
Non-Network Mental Health Professionals:
National Impact Survey ............................................................................
Non-Network Non-Mental Health Professionals:
National Impact Survey ............................................................................
Non-Network product developers:
Case Study Interviews ..............................................................................
Total ...................................................................................................
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Product development and
dissemination will be evaluated with
data that will be collected from 44
project directors/principal investigators.
These data will be collected annually.
To assess the national impact of the
NCTSN, data will be collected from
1,600 mental health and 1,600 nonmental health service providers from
outside the NCTSN. These data will be
collected every second year over the
four years of the evaluation (i.e., two
data collection points per respondent).
The average annual respondent
burden is estimated below.
Annual number of
responses/
respondent
Hours per
response
Total annual
hours
3,000
3,000
3,000
3,000
2,185
10
2
2
2
2
1
1
0.33
0.22
0.22
0.22
0.08
1.50
1980
1320
1320
1320
175
15
2,121
2,121
2
2
0.33
0.17
1400
721
18
54
1,100
1,100
50
1
1
1
1
1
0.50
1.00
0.50
0.50
0.50
9
54
550
550
25
18
18
44
44
44
10
44
1
1
1
1
1
1
1
0.50
1.00
0.50
1.50
0.50
0.50
1.00
9
18
22
66
22
5
44
4
44
35
20
44
30
44
400
1
1
1
1
1
1
1
1
0.50
0.50
1.50
2.00
0.50
0.50
1.00
0.75
2
22
53
40
22
15
44
300
1,600
1
0.50
800
1,600
1
0.50
800
20
1
1.50
30
8,564
........................
........................
11,753
E:\FR\FM\22APN1.SGM
22APN1
20922
Federal Register / Vol. 70, No. 77 / Friday, April 22, 2005 / Notices
Send comments to Summer King,
SAMHSA Reports Clearance Officer,
Room 7–1044, 1 Choke Cherry Road,
Rockville, MD 20850. Written comments
should be received by June 21, 2005.
Dated: April 14, 2005.
Anna Marsh,
Executive Officer, SAMHSA.
[FR Doc. 05–7988 Filed 4–21–05; 8:45 am]
BILLING CODE 4162–20–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 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.
Proposed Project: Drug and Alcohol
Services Information System (DASIS)—
(OMB No. 0930–0106)—Revision
The DASIS consists of three related
data systems: the Inventory of Substance
Abuse Treatment Services (I–SATS );
the National Survey of Substance Abuse
Treatment Services (N–SSATS), and the
Treatment Episode Data Set (TEDS). The
I–SATS includes all substance abuse
treatment facilities known to SAMHSA.
The N–SSATS is an annual survey of all
substance abuse treatment facilities
listed in the I–SATS. The TEDS is a
compilation of client-level admission
data and discharge data submitted by
States on clients treated in facilities that
receive State funds. Together, the three
DASIS components provide information
on the location, scope and
characteristics of all known drug and
alcohol treatment facilities in the United
States, the number of persons in
treatment, and the characteristics of
clients receiving services at publiclyfunded facilities. This information is
needed to assess the nature and extent
of these resources, to identify gaps in
services, to provide a database for
treatment referrals, and to assess
demographic and substance-related
trends in treatment.
The request for OMB approval will
include several changes to the 2006 N–
SSATS questionnaire, including:
modification of the treatment categories
to better reflect the practices and
terminology currently used in the
treatment field; modification of the
detoxification question, including the
addition of a follow-up question on
whether the facility uses drugs in
detoxification and for which substances;
the addition of nicotine replacement
therapy and psychiatric medications to
the pharmacotherapies list; the addition
of questions on treatment approaches
and behavioral interventions; the
addition of new services to the list of
services provided; the addition of a
question on quality control procedures
used by the facility; and, the addition of
a question on whether the facility
accepts Access to Recovery (ATR)
vouchers and how many annual
admissions were funded by ATR
vouchers. The remaining sections of the
N–SSATS questionnaire will remain
unchanged except for minor
modifications to wording. The OMB
request will also include the addition of
several new data elements to the TEDS
client-level record. To the extent that
states already collect the elements from
their treatment providers, the following
elements will be included in the TEDS
data collection: number of arrests,
substances used at discharge,
employment at discharge, and living
arrangement at discharge. The
additional data elements are being
requested by the Center for Substance
Abuse Treatment, SAMHSA, for use in
estimating national treatment outcomes.
No significant changes are expected in
the other DASIS activities.
Estimated annual burden for the
DASIS activities is shown below:
Number of respondents
Hours per respondent
Hours per response
STATES:
TEDS Admission Data ..............................................................................
TEDS Discharge Data ..............................................................................
TEDS Discharge Crosswalks ...................................................................
I–SATS Update1 ................................................................................
52
40
5
56
4
4
1
67
6
8
10
.08
1,248
1,280
50
300
State Subtotal ....................................................................................
56
........................
........................
2,878
FACILITIES:
I–SATS Update2 .......................................................................................
Pretest of N–SSATS revisions .................................................................
Augmentation Screener ............................................................................
N–SSATS Questionnaire ..........................................................................
Mini N–SSATS ..........................................................................................
100
200
500
19,000
700
1
1
1
1
1
.08
.37
.08
.67
.4
8
74
40
12,730
280
Facility Subtotal .................................................................................
20,500
........................
........................
13,132
TOTAL ........................................................................................
20,556
........................
........................
16,010
Type of respondent and activity
Total burden
hours
1 States forward to SAMHSA information on newly licensed/approved facilities and on changes in facility name, address, status, etc. This is
done electronically by nearly all States.
2 Facilities forward to SAMHSA information on new facilities and on changes to existing facilities. This can be done by fax or e-mail.
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E:\FR\FM\22APN1.SGM
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]]>Agencies
[Federal Register Volume 70, Number 77 (Friday, April 22, 2005)]
[Notices]
[Pages 20920-20922]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: 05-7988]
-----------------------------------------------------------------------
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 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.
Proposed Project: Cross-Site Evaluation of the National Child Traumatic
Stress Initiative (NCTSI)--NEW
The Substance Abuse and Mental Health Services Administration's
(SAMHSA), Center for Mental Health Services (CMHS) will conduct the
Cross-Site Evaluation of the National Child Traumatic Stress Initiative
(NCTSI). The data collected will describe the children and families
served by the National Child Traumatic Stress Network (NCTSN) and their
outcomes, assess the development and dissemination of effective
treatments and services, evaluate intra-network collaboration, and
assess the Network's impact beyond the NCTSN.
Data will be collected from caregivers, NCTSN staff (e.g., project
directors, researchers, and providers), mental health providers outside
of the NCTSN, and non-mental health service providers who provide
services to children outside of the NCTSN. Data collection will take
place in 31 Community Treatment and Services Programs (CTS), 13
Treatment and Service Adaptation Centers (TSA), and 2 National Centers
for Child Traumatic Stress (NCCTS). Data collection for this evaluation
will be conducted over a four-year period.
In order to describe the children served, their outcomes, and
satisfaction with services, data will be collected from youth ages 7-18
who are receiving services in the NCTSN, and from caregivers for all
children who are receiving NCTSN services. Data will be collected when
the child/youth enters services and during subsequent follow-up
sessions at three-month intervals over the course of one year.
[[Page 20921]]
Approximately 2,121 youth and 3,000 caregivers will participate in the
evaluation.
Data will be collected for use in the development of evaluation
measures that will assess the development, dissemination and adoption
of trauma-informed services. These data will be collected from a total
of approximately 110 NCTSN service providers, project directors and
NCCTS staff. Data will be collected one time from these respondents.
Measures that collect data on development, dissemination, and
adoption of trauma-informed services and other NCTSN products will be
administered to approximately 1,100 service providers, 44 project
directors, and 44 researchers/evaluators. These measures will be
administered once per year in each of the four years of the evaluation.
To assess collaboration across the network, data will be collected
from approximately 450 NCTSI staff and 44 project directors/principal
investigators. The surveys associated with this data collection will be
administered at varying intervals, with either one or two data
collection points per respondent over the four years of the evaluation.
Product development and dissemination will be evaluated with data
that will be collected from 44 project directors/principal
investigators. These data will be collected annually.
To assess the national impact of the NCTSN, data will be collected
from 1,600 mental health and 1,600 non-mental health service providers
from outside the NCTSN. These data will be collected every second year
over the four years of the evaluation (i.e., two data collection points
per respondent).
The average annual respondent burden is estimated below.
----------------------------------------------------------------------------------------------------------------
Annual number
Instrument Number of of responses/ Hours per Total annual
respondents respondent response hours
----------------------------------------------------------------------------------------------------------------
Caregivers:
Child Behavior Checklist 1.5-5/6-18......... 3,000 2 0.33 1980
Service Summary Form........................ 3,000 2 0.22 1320
Baseline/Renewal Assessment................. 3,000 2 0.22 1320
Core Clinical Characteristics Form.......... 3,000 2 0.22 1320
Youth Services Survey for Families.......... 2,185 1 0.08 175
Case Study Interviews....................... 10 1 1.50 15
Youth:
Trauma Symptoms Checklist for Children- 2,121 2 0.33 1400
Abbreviated................................
UCLA-PTSD short form........................ 2,121 2 0.17 721
Network Service Provider:
Key Informant Interviews.................... 18 1 0.50 9
Focus Groups................................ 54 1 1.00 54
Trauma-informed Service Provider Survey..... 1,100 1 0.50 550
General Adoption Assessment Survey.......... 1,100 1 0.50 550
Adoption and Implementation Factors 50 1 0.50 25
Interview..................................
Project Director/Principal Investigator:
Key Informant Interviews.................... 18 1 0.50 9
Focus Groups................................ 18 1 1.00 18
Trauma-informed Service Provider Survey..... 44 1 0.50 22
Product/Innovations Development and 44 1 1.50 66
Dissemination Survey.......................
General Adoption Assessment Survey.......... 44 1 0.50 22
Adoption and Implementation Factors 10 1 0.50 5
Interview..................................
Network Survey.............................. 44 1 1.00 44
Other Network Staff:
Key Informant Interviews.................... 4 1 0.50 2
Trauma-informed Service Provider Survey..... 44 1 0.50 22
Telephone Interviews........................ 35 1 1.50 53
Case study interviews....................... 20 1 2.00 40
General Adoption Assessment Survey.......... 44 1 0.50 22
Adoption and Implementation Factors 30 1 0.50 15
Interview..................................
Network Survey.............................. 44 1 1.00 44
Partner Participatory Assessment Tool....... 400 1 0.75 300
Non-Network Mental Health Professionals:
National Impact Survey...................... 1,600 1 0.50 800
Non-Network Non-Mental Health Professionals:
National Impact Survey...................... 1,600 1 0.50 800
Non-Network product developers:
Case Study Interviews....................... 20 1 1.50 30
-----------------
Total................................... 8,564 .............. .............. 11,753
----------------------------------------------------------------------------------------------------------------
[[Page 20922]]
Send comments to Summer King, SAMHSA Reports Clearance Officer,
Room 7-1044, 1 Choke Cherry Road, Rockville, MD 20850. Written comments
should be received by June 21, 2005.
Dated: April 14, 2005.
Anna Marsh,
Executive Officer, SAMHSA.
[FR Doc. 05-7988 Filed 4-21-05; 8:45 am]
BILLING CODE 4162-20-P
