Alzheimer's Disease Supportive Services Program (ADSSP) Data Collection

ICR 201006-0985-001

OMB: 0985-0022

Federal Form Document

Forms and Documents
Document
Name
Status
Supplementary Document
2010-08-04
Supplementary Document
2010-05-20
Supplementary Document
2010-08-04
Supplementary Document
2010-05-19
Supplementary Document
2010-05-20
Supporting Statement A
2010-08-04
IC Document Collections
ICR Details
0985-0022 201006-0985-001
Historical Active 200703-0985-001
HHS/ACL
Alzheimer's Disease Supportive Services Program (ADSSP) Data Collection
Revision of a currently approved collection   No
Regular
Approved with change 08/11/2010
Retrieve Notice of Action (NOA) 06/07/2010
  Inventory as of this Action Requested Previously Approved
08/31/2013 36 Months From Approved 08/31/2010
94 0 38
1,410 0 950
0 0 0

The Alzheimer's Disease Supportive Services Program (ADSSP) was established under Section 398 of the Public Health Service Act (P.L. 78-410; 42 U.S.C. 280c-3). It was amended by the Home Health Care and Alzheimer's Disease Amendments of 1990 (PL 101-557) and by the Health Professions Education Partnerships Act of 1998 (PL 105-392). The ADSSP is administered by the Administration on Aging (AoA) within the U.S. Department of Health and Human Services. The ADSSP program helps states extend supports and services to persons with dementia and their family caregivers, with a focus on underserved populations. The PHS Act requires AoA to "provide for an evaluation of each demonstration project for which a grant is made." In compliance with the PHS Act, AoA developed a new State data collection protocol that will require future ADSSP state grantees (those funded starting in FY 2011) to transmit semi-annual data to AoA. In December 2009, AoA initiated a review of the current ADSSP-Data Reporting Tool (ADSSP-DRT) to ensure the acceptability of these items for evaluating the program and minimizing burden for respondents. This review included experts in the field of Alzheimer's disease and long-term care who are familiar with the program, as well as current ADSSP grantees. Feedback was provided by phone and e-mail over a period of 4 months. The result of this input is the revised ADSSP-DRT and supporting documents. As with the current ADSSP-DRT, AoA will work with ADSSP grantees to ensure easy access to a reporting system and offer regular training in using the tool to ensure minimal burden for program grantees.

PL: Pub.L. 101 - 557 398 399 399A Name of Law: Home Health Care and Alzheimer's Disease Amendment of 1990
   PL: Pub.L. 78 - 410 398 Name of Law: Public Health Service Act
   PL: Pub.L. 105 - 392 302 Name of Law: Health Professions Education Partnerships Act
  
None

Not associated with rulemaking

  75 FR 12241 03/15/2010
75 FR 28809 05/24/2010
Yes

1
IC Title Form No. Form Name
Alzheimer's Disease Supportive Services Program (ADSSP) Data Collection

  Total Approved Previously Approved Change Due to New Statute Change Due to Agency Discretion Change Due to Adjustment in Estimate Change Due to Potential Violation of the PRA
Annual Number of Responses 94 38 0 56 0 0
Annual Time Burden (Hours) 1,410 950 0 460 0 0
Annual Cost Burden (Dollars) 0 0 0 0 0 0
Yes
Miscellaneous Actions
No
The annual reporting burden hour estimates have increased from 950 hours to 1410 hours for the following reasons: o The new estimates are for 47 grantee respondents, rather than the 38 grantee respondents from the original ADSSP-DRT approval. o Although, for the current data set, it was anticipated that grantee respondents would spend 25 hours spent reporting annually, the actual number of hours spent, as reported by the current ADSSP state grantees consulted, was 15 hours annually. o The frequency of data reporting will increase from annually to semi-annually. The annual reporting burden for grantees is anticipated to be 30 hours (15 twice yearly x 2). This is likely an over-estimate because several items included in the current tool are not included in the revised tool. Refinements have also been made to the supporting documents in order to streamline the data collection template and data definitions. The proposed move from annual to semi-reporting came as a result of a re-evaluation of the ADSSP-DRT by AoA, experts in the field of Alzheimer's disease and long-term care, and current ADSSP state grantees. Based on the collection experiences over the past three years, AoA and the expert reviewers believe that more frequent data collection would be helpful in order to comply with the requirements of the PHS Act, for federal level advocacy and for management of the program; all ADSSP state grantees consulted believed that more up-to-date information would be helpful for state-level advocacy.

$22,288
No
No
No
Uncollected
No
Uncollected
Harry Posman 2023573540

  No

On behalf of this Federal agency, I certify that the collection of information encompassed by this request complies with 5 CFR 1320.9 and the related provisions of 5 CFR 1320.8(b)(3).
The following is a summary of the topics, regarding the proposed collection of information, that the certification covers:
 
 
 
 
 
 
 
    (i) Why the information is being collected;
    (ii) Use of information;
    (iii) Burden estimate;
    (iv) Nature of response (voluntary, required for a benefit, or mandatory);
    (v) Nature and extent of confidentiality; and
    (vi) Need to display currently valid OMB control number;
 
 
 
If you are unable to certify compliance with any of these provisions, identify the item by leaving the box unchecked and explain the reason in the Supporting Statement.
06/07/2010


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