Agency Information Collection Activities: Proposed Collection; Comment Request, 75568-75570 [E6-21350]
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Federal Register / Vol. 71, No. 241 / Friday, December 15, 2006 / Notices
Data collection per
respondents
Hours per data
collection
Total hour
burden
Type of response
Number of respondents
Client Baseline Assessment .................................
Periodic Client Reassessment .............................
Discharge Interviews ............................................
Chart Abstraction ..................................................
17,555 ...........................................
7,015 (3-month) ............................
6,532 (6-month) ............................
4,409 .............................................
7,015 (3-month) ............................
6,532 (6-month) ............................
11,023 (Discharge) .......................
1
1
1
1
1
1
1
0.333
0.333
0.333
0.333
0.1
0.1
0.1
5,852
2,338
2,178
1,470
702
653
1,102
Total ..............................................................
17,555 ...........................................
..............................
..............................
14,294
Written comments and
recommendations concerning the
proposed information collection should
be sent by January 16, 2007 to:
SAMHSA Desk Officer, Human
Resources and Housing Branch, Office
of Management and Budget, New
Executive Office Building, Room 10235,
Washington, DC 20503; due to potential
delays in OMB’s receipt and processing
of mail sent through the U.S. Postal
Service, respondents are encouraged to
submit comments by fax to: 202–395–
6974.
Dated: December 7, 2006.
Elaine Parry,
Acting Director, Office of Program Services.
[FR Doc. E6–21349 Filed 12–14–06; 8:45 am]
BILLING CODE 4162–20–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Substance Abuse and Mental Health
Services Administration
mstockstill on PROD1PC61 with NOTICES
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;
VerDate Aug<31>2005
17:18 Dec 14, 2006
Jkt 211001
(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: National Evaluation
of the Comprehensive Community
Mental Health Services for Children
and Their Families Program: Phase
IV—(OMB No. 0930–0257)—Revision
SAMHSA’s Center for Mental Health
Services is responsible for the national
evaluation of the Comprehensive
Community Mental Health Services for
Children and Their Families Program
that will collect data on child mental
health outcomes, family life, and service
system development and performance.
The national evaluation of the
Comprehensive Community Mental
Health Services for Children and Their
Families Program will collect data on
child mental health outcomes, family
life, and service system development
and performance. Data will be collected
on 27 service systems, and roughly
5,922 children and families. Data
collection for this evaluation is
conducted over a 5-year period. The
core of service system data will be
collected every 18 months throughout
the 5-year evaluation period, with a
sustainability survey conducted in
selected years. Service delivery and
system variables of interest include the
following: Maturity of system of care
development, adherence to the system
of care program model, and client
service experience. The length of time
that individual families will participate
in the study ranges from 18 to 36
months depending on when they enter
the evaluation. Child and family
outcomes of interest will be collected at
intake and during subsequent follow-up
PO 00000
Frm 00094
Fmt 4703
Sfmt 4703
sessions at 6-month intervals. The
outcome measures include the
following: Child symptomatology and
functioning, family functioning,
material resources, and caregiver strain.
Time-limited studies addressing the
cultural competence of services and the
role of primary care providers in
systems of care will be conducted at
selected points during the evaluation
period. Internet-based technology will
be used for collecting data via Webbased surveys and for data entry and
management. The average annual
respondent burden is estimated below
for the final 3 years of data collection.
The estimate reflects the average
number of respondents in each
respondent category, the average
number of responses per respondent per
year, the average length of time it will
take for each response, and the total
average annual burden for each category
of respondent, and for all categories of
respondents combined.
This revision to the currently
approved information collection
activities includes: (1) The addition of a
Primary Care Study, and (2) the addition
of a Treatment Effectiveness Study. The
Primary Care Study seeks to investigate
the role of primary health care
practitioners (PCPs) in systems of care
and to further understand the impact of
services provided within primary care
on child and family outcomes. One goal
of this study is to identity strategies that
help primary care and mental health
care providers to work together
effectively. Another is to identify ways
to integrate PCPs into systems of care.
The treatment effectiveness study will
examine the relative impact of
community-based treatments focused
within system of care sites. This study
will focus on a community-based
practice that has not accumulated
research evidence, but rather through
community-based implementation that
has accumulated practice-based
evidence.
E:\FR\FM\15DEN1.SGM
15DEN1
75569
Federal Register / Vol. 71, No. 241 / Friday, December 15, 2006 / Notices
Instrument
Number of
respondents
Respondent
Total average
number of
responses per
respondent
Hours per
response
Total burden
hours
3-Year
average annual burden
hours
System-of-Care Assessment
Interview Guides and Data Collection
Forms.
Interagency
Collaboration
Scale
(IACS).
Key site informants.
Key site informants.
648
2
1.000
1296
432
648
2
0.133
173
58
Cross-Sectional Descriptive Study
Caregiver Information Questionnaire
(CIQ–IC).
Caregiver Information Questionnaire
Followup (CIQ–FC).
Caregiver .............
5922
1
0.283
1676
559
Caregiver .............
5922
3
0.200
3553
1184
Child and Family Outcome Study
Caregiver
Strain
Questionnaire
(CGSQ).
Child Behavior Checklist (CBCL)/
Child Behavior Checklist 11⁄2–5
(CBCL 11⁄2–5).
Education Questionnaire (EQ) ...........
Living Situations Questionnaire (LSQ)
The Family Life Questionnaire (FLQ)
Behavioral and Emotional Rating
Scale (BERS).
Columbia Impairment Scale (CIS) .....
The Vineland Screener (VS) .............
Cultural Competence and Service
Provision—Caregiver (CCSP).
Delinquency Survey (DS) ..................
Behavioral and Emotional Rating
Scale—Second Edition, Youth Rating Scale (BERS–2).
Gain-quick Substance Related Issues
(Gain SRI).
Substance Use Scale (SUS) .............
Revised Children’s Manifest Anxiety
Scales (RCMAS).
Reynolds Adolescent Depression
Scale—Second Edition (RADS–2).
Youth
Information
Questionnaire
(YIQ–I).
Youth
Information
Questionnaire
(YIQ–F).
Caregiver .............
5922
4
0.167
3956
1319
Caregiver .............
5922
4
0.333
7888
2629
Caregiver
Caregiver
Caregiver
Caregiver
.............
.............
.............
.............
5922
5922
5922
5922
4
4
4
4
0.100
0.083
0.054
0.167
2369
1966
1184
3956
790
655
395
1319
Caregiver .............
Caregiver .............
Caregiver .............
5922
2665
5922
4
4
3
0.083
0.250
0.167
1966
2665
2967
655
888
989
Youth ...................
Youth ...................
3553
3553
4
4
0.167
0.167
2374
2374
791
791
Youth ...................
3553
4
0.083
1180
1966
Youth ...................
Youth ...................
3553
3553
4
4
0.100
0.050
1421
711
474
237
Youth ...................
3553
4
0.050
711
237
Youth ...................
3553
1
0.167
593
198
Youth ...................
3553
3
0.167
1780
593
Service Experience Study
Multi-Sector Services Contact—Revised for Caregiver (MSSC–RC).
Youth Services Survey for Families
(YSS–F).
Cultural Competence Practices Study
(Focus Group).
Cultural Competence Practices Study
(Focus Group).
Youth Services Survey (YSS–Y) .......
Cultural Competence Practices Study
(Focus Group).
Caregiver .............
5922
3
0.250
4442
1481
Caregiver .............
5922
3
0.117
2079
693
Caregiver .............
36
1
1.500
54
18
Youth ...................
36
1
1.500
54
18
Youth ...................
Provider ...............
3553
60
4
1
0.083
1.500
1180
90
393
30
mstockstill on PROD1PC61 with NOTICES
Treatment Effectiveness Study
Conflict
Behavior
Questionnaire
(CBQ).
Family Assessment Measure (FAM)
Therapeutic Alliance Scale—Caregiver (TAS).
Ohio Scales—Caregiver ....................
Parenting Sense of Competence
Scale (PSOC).
Parenting Locus of Control (PLOC) ..
Therapy Adherence Form ..................
VerDate Aug<31>2005
15:47 Dec 14, 2006
Caregiver .............
400
4
0.167
267
89
Caregiver .............
Caregiver .............
400
400
4
4
0.250
0.167
400
267
133
89
Caregiver .............
Caregiver .............
400
400
4
4
0.250
0.167
400
267
133
89
Caregiver .............
Caregiver .............
400
400
4
4
0.250
0.167
400
267
133
89
Jkt 211001
PO 00000
Frm 00095
Fmt 4703
Sfmt 4703
E:\FR\FM\15DEN1.SGM
15DEN1
75570
Federal Register / Vol. 71, No. 241 / Friday, December 15, 2006 / Notices
Number of
respondents
Total average
number of
responses per
respondent
Hours per
response
Total burden
hours
3-Year
average annual burden
hours
Instrument
Respondent
Therapeutic Alliance Scale—Youth
(TAS–Y).
Ohio Scales—Youth ..........................
Youth ...................
240
4
0.167
160
53
Youth ...................
240
4
0.250
240
80
1
0.500
270
90
2
2
0.500
0.500
27
81
9
27
Primary Care Provider Study
Primary Care Provider—Web survey
Provider ...............
540
Sustainability Study
Sustainability Web Survey .................
Sustainability Survey—Provider ........
Caregiver .............
Provider/Administrator.
27
81
SUMMARY OF ANNUALIZED BURDEN ESTIMATES FOR 3 YEARS
Number of
distinct respondents
Number of
responses per
respondent
Average burden per
response
(hours)
Total average
annual burden
(hours)
Caregivers ........................................................................................................
Youth ................................................................................................................
Provider/Administrators ....................................................................................
5922
3553
648
1.15
1.19
0.57
2.10
1.01
1.74
14339
4259
637
Total ..........................................................................................................
10123
........................
........................
19234
Send comments to Summer King,
SAMHSA Reports Clearance Officer,
Room 7–1044, 1 Choke Cherry Road,
Rockville, MD 20857. Written comments
should be received within 60 days of
this notice.
Dated: December 7, 2006.
Elaine Parry,
Acting Director, Office of Program Services.
[FR Doc. E6–21350 Filed 12–14–06; 8:45 am]
BILLING CODE 4162–20–P
DEPARTMENT OF HOUSING AND
URBAN DEVELOPMENT
[Docket No. FR–5037–N–91]
Notice of Submission of Proposed
Information Collection to OMB; Alaska
Native/Native Hawaiian Institutions
Assisting Communities (AN/NHAIC)
Office of the Chief Information
Officer, HUD.
ACTION: Notice.
mstockstill on PROD1PC61 with NOTICES
AGENCY:
SUMMARY: The proposed information
collection requirement described below
has been submitted to the Office of
Management and Budget (OMB) for
review, as required by the Paperwork
Reduction Act. The Department is
soliciting public comments on the
subject proposal.
Alaska Native/Native Hawaiian
colleges and universities apply for
competitive grants to undertake
VerDate Aug<31>2005
15:47 Dec 14, 2006
Jkt 211001
Community Development Block Grant
(CDBG)-eligible activities to expand
their role helping their communities
with neighborhood revitalization,
housing, and economic development.
DATES: Comments Due Date: January 16,
2007.
ADDRESSES: Interested persons are
invited to submit comments regarding
this proposal. Comments should refer to
the proposal by name and/or OMB
approval Number (2528–0206) and
should be sent to: HUD Desk Officer,
Office of Management and Budget, New
Executive Office Building, Washington,
DC 20503; fax: 202–395–6974.
FOR FURTHER INFORMATION CONTACT:
Lillian Deitzer, Departmental Reports
Management Officer, QDAM,
Department of Housing and Urban
Development, 451 Seventh Street, SW.,
Washington, DC 20410; e-mail
Lillian_L._Deitzer@HUD.gov or
telephone (202) 708–2374. This is not a
toll-free number. Copies of available
documents submitted to OMB may be
obtained from Ms. Deitzer or from
HUD’s Web site at https://
hlannwp031.hud.gov/po/i/icbts/
collectionsearch.cfm.
This
notice informs the public that the
Department of Housing and Urban
Development has submitted to OMB a
request for approval of the information
collection described below. This notice
is soliciting comments from members of
SUPPLEMENTARY INFORMATION:
PO 00000
Frm 00096
Fmt 4703
Sfmt 4703
the public and affecting agencies
concerning the proposed collection of
information to: (1) Evaluate whether the
proposed collection of information is
necessary for the proper performance of
the functions of the agency, including
whether the information will have
practical utility; (2) Evaluate the
accuracy of the agency’s estimate of the
burden of the proposed collection of
information; (3) Enhance the quality,
utility, and clarity of the information to
be collected; and (4) Minimize the
burden of the collection of information
on those who are to respond; including
through the use of appropriate
automated collection techniques or
other forms of information technology,
e.g., permitting electronic submission of
responses.
This notice also lists the following
information:
Title of Proposal: Alaska Native/
Native Hawaiian Institutions Assisting
Communities (AN/NHAIC).
OMB Approval Number: 2528–0206.
Form Numbers: SF–424, SF–424
Supplement, SF–LLL, HUD–424–CB,
HUD–27300, HUD–2880, HUD–2993,
HUD–96011, HUD–2994–A and HUD–
96010 and HUD–2993.
Description of the Need for the
Information and its Proposed Use:
Alaska Native/Native Hawaiian colleges
and universities apply for competitive
grants to undertake Community
Development Block Grant (CDBG)eligible activities to expand their role
E:\FR\FM\15DEN1.SGM
15DEN1
]]>Agencies
[Federal Register Volume 71, Number 241 (Friday, December 15, 2006)]
[Notices]
[Pages 75568-75570]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: E6-21350]
-----------------------------------------------------------------------
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.
Proposed Project: National Evaluation of the Comprehensive Community
Mental Health Services for Children and Their Families Program: Phase
IV--(OMB No. 0930-0257)--Revision
SAMHSA's Center for Mental Health Services is responsible for the
national evaluation of the Comprehensive Community Mental Health
Services for Children and Their Families Program that will collect data
on child mental health outcomes, family life, and service system
development and performance.
The national evaluation of the Comprehensive Community Mental
Health Services for Children and Their Families Program will collect
data on child mental health outcomes, family life, and service system
development and performance. Data will be collected on 27 service
systems, and roughly 5,922 children and families. Data collection for
this evaluation is conducted over a 5-year period. The core of service
system data will be collected every 18 months throughout the 5-year
evaluation period, with a sustainability survey conducted in selected
years. Service delivery and system variables of interest include the
following: Maturity of system of care development, adherence to the
system of care program model, and client service experience. The length
of time that individual families will participate in the study ranges
from 18 to 36 months depending on when they enter the evaluation. Child
and family outcomes of interest will be collected at intake and during
subsequent follow-up sessions at 6-month intervals. The outcome
measures include the following: Child symptomatology and functioning,
family functioning, material resources, and caregiver strain. Time-
limited studies addressing the cultural competence of services and the
role of primary care providers in systems of care will be conducted at
selected points during the evaluation period. Internet-based technology
will be used for collecting data via Web-based surveys and for data
entry and management. The average annual respondent burden is estimated
below for the final 3 years of data collection. The estimate reflects
the average number of respondents in each respondent category, the
average number of responses per respondent per year, the average length
of time it will take for each response, and the total average annual
burden for each category of respondent, and for all categories of
respondents combined.
This revision to the currently approved information collection
activities includes: (1) The addition of a Primary Care Study, and (2)
the addition of a Treatment Effectiveness Study. The Primary Care Study
seeks to investigate the role of primary health care practitioners
(PCPs) in systems of care and to further understand the impact of
services provided within primary care on child and family outcomes. One
goal of this study is to identity strategies that help primary care and
mental health care providers to work together effectively. Another is
to identify ways to integrate PCPs into systems of care. The treatment
effectiveness study will examine the relative impact of community-based
treatments focused within system of care sites. This study will focus
on a community-based practice that has not accumulated research
evidence, but rather through community-based implementation that has
accumulated practice-based evidence.
[[Page 75569]]
--------------------------------------------------------------------------------------------------------------------------------------------------------
Total average
Number of number of Hours per Total burden 3-Year
Instrument Respondent respondents responses per response hours average annual
respondent burden hours
--------------------------------------------------------------------------------------------------------------------------------------------------------
System-of-Care Assessment
--------------------------------------------------------------------------------------------------------------------------------------------------------
Interview Guides and Data Collection Forms Key site informants......... 648 2 1.000 1296 432
Interagency Collaboration Scale (IACS).... Key site informants......... 648 2 0.133 173 58
--------------------------------------------------------------------------------------------------------------------------------------------------------
Cross-Sectional Descriptive Study
--------------------------------------------------------------------------------------------------------------------------------------------------------
Caregiver Information Questionnaire (CIQ- Caregiver................... 5922 1 0.283 1676 559
IC).
Caregiver Information Questionnaire Caregiver................... 5922 3 0.200 3553 1184
Followup (CIQ-FC).
--------------------------------------------------------------------------------------------------------------------------------------------------------
Child and Family Outcome Study
--------------------------------------------------------------------------------------------------------------------------------------------------------
Caregiver Strain Questionnaire (CGSQ)..... Caregiver................... 5922 4 0.167 3956 1319
Child Behavior Checklist (CBCL)/Child Caregiver................... 5922 4 0.333 7888 2629
Behavior Checklist 1\1/2\-5 (CBCL 1\1/2\-
5).
Education Questionnaire (EQ).............. Caregiver................... 5922 4 0.100 2369 790
Living Situations Questionnaire (LSQ)..... Caregiver................... 5922 4 0.083 1966 655
The Family Life Questionnaire (FLQ)....... Caregiver................... 5922 4 0.054 1184 395
Behavioral and Emotional Rating Scale Caregiver................... 5922 4 0.167 3956 1319
(BERS).
Columbia Impairment Scale (CIS)........... Caregiver................... 5922 4 0.083 1966 655
The Vineland Screener (VS)................ Caregiver................... 2665 4 0.250 2665 888
Cultural Competence and Service Provision-- Caregiver................... 5922 3 0.167 2967 989
Caregiver (CCSP).
Delinquency Survey (DS)................... Youth....................... 3553 4 0.167 2374 791
Behavioral and Emotional Rating Scale-- Youth....................... 3553 4 0.167 2374 791
Second Edition, Youth Rating Scale (BERS-
2).
Gain-quick Substance Related Issues (Gain Youth....................... 3553 4 0.083 1180 1966
SRI).
Substance Use Scale (SUS)................. Youth....................... 3553 4 0.100 1421 474
Revised Children's Manifest Anxiety Scales Youth....................... 3553 4 0.050 711 237
(RCMAS).
Reynolds Adolescent Depression Scale-- Youth...................... 3553 4 0.050 711 237
Second Edition (RADS-2).
Youth Information Questionnaire (YIQ-I)... Youth....................... 3553 1 0.167 593 198
Youth Information Questionnaire (YIQ-F)... Youth....................... 3553 3 0.167 1780 593
--------------------------------------------------------------------------------------------------------------------------------------------------------
Service Experience Study
--------------------------------------------------------------------------------------------------------------------------------------------------------
Multi-Sector Services Contact--Revised for Caregiver................... 5922 3 0.250 4442 1481
Caregiver (MSSC-RC).
Youth Services Survey for Families (YSS-F) Caregiver................... 5922 3 0.117 2079 693
Cultural Competence Practices Study (Focus Caregiver................... 36 1 1.500 54 18
Group).
Cultural Competence Practices Study (Focus Youth....................... 36 1 1.500 54 18
Group).
Youth Services Survey (YSS-Y)............. Youth....................... 3553 4 0.083 1180 393
Cultural Competence Practices Study (Focus Provider.................... 60 1 1.500 90 30
Group).
--------------------------------------------------------------------------------------------------------------------------------------------------------
Treatment Effectiveness Study
--------------------------------------------------------------------------------------------------------------------------------------------------------
Conflict Behavior Questionnaire (CBQ)..... Caregiver................... 400 4 0.167 267 89
Family Assessment Measure (FAM)........... Caregiver................... 400 4 0.250 400 133
Therapeutic Alliance Scale--Caregiver Caregiver................... 400 4 0.167 267 89
(TAS).
Ohio Scales--Caregiver.................... Caregiver................... 400 4 0.250 400 133
Parenting Sense of Competence Scale (PSOC) Caregiver................... 400 4 0.167 267 89
Parenting Locus of Control (PLOC)......... Caregiver................... 400 4 0.250 400 133
Therapy Adherence Form.................... Caregiver................... 400 4 0.167 267 89
[[Page 75570]]
Therapeutic Alliance Scale--Youth (TAS-Y). Youth....................... 240 4 0.167 160 53
Ohio Scales--Youth........................ Youth....................... 240 4 0.250 240 80
--------------------------------------------------------------------------------------------------------------------------------------------------------
80Primary Care Provider Study
--------------------------------------------------------------------------------------------------------------------------------------------------------
Primary Care Provider--Web survey......... Provider.................... 540 1 0.500 270 90
--------------------------------------------------------------------------------------------------------------------------------------------------------
Sustainability Study
--------------------------------------------------------------------------------------------------------------------------------------------------------
Sustainability Web Survey................. Caregiver................... 27 2 0.500 27 9
Sustainability Survey--Provider........... Provider/Administrator...... 81 2 0.500 81 27
--------------------------------------------------------------------------------------------------------------------------------------------------------
Summary of Annualized Burden Estimates for 3 Years
----------------------------------------------------------------------------------------------------------------
Number of Number of Average burden Total average
distinct responses per per response annual burden
respondents respondent (hours) (hours)
----------------------------------------------------------------------------------------------------------------
Caregivers...................................... 5922 1.15 2.10 14339
Youth........................................... 3553 1.19 1.01 4259
Provider/Administrators......................... 648 0.57 1.74 637
---------------------------------------------------------------
Total....................................... 10123 .............. .............. 19234
----------------------------------------------------------------------------------------------------------------
Send comments to Summer King, SAMHSA Reports Clearance Officer,
Room 7-1044, 1 Choke Cherry Road, Rockville, MD 20857. Written comments
should be received within 60 days of this notice.
Dated: December 7, 2006.
Elaine Parry,
Acting Director, Office of Program Services.
[FR Doc. E6-21350 Filed 12-14-06; 8:45 am]
BILLING CODE 4162-20-P
