Attachment_6A-0990-PatientCentered

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Patient Centered Care Collaboration to Improve Minority Health Project

Attachment_6A-0990-PatientCentered

OMB: 0990-0402

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Shape2 59130 Federal Register / Vol. 76, No. 185 / Friday, September 23, 2011 / Notices


Keith Tucker,

Office of the Secretary, Paperwork Reduction

Act Reports Clearance Officer.

[FR Doc. 2011–24495 Filed 9–22–11; 8:45 am]

BILLING CODE 4150–46–P

proposed paperwork collections referenced above, e-mail your request, including your address, phone number, OMB number, and OS document identifier, to Sherette.funncoleman@

program participants; if the approach taken through the implementation of proven PCOR findings such as using community health workers and educators, and pharmacists to deliver

hhs.gov, or call the Reports Clearance

Office on (202) 690–6162. Written

the interventions improves the

likelihood of patients changing their

DEPARTMENT OF HEALTH AND

HUMAN SERVICES


[Document Identifier: OS–0990–New; 60- Day Notice]


Agency Information Collection Request; 60-Day Public Comment Request

AGENCY: Office of the Secretary, HHS. In compliance with the requirement

of section 3506(c)(2)(A) of the

Paperwork Reduction Act of 1995, the Office of the Secretary (OS), Department of Health and Human Services, is publishing the following summary of a proposed information collection request for public comment. Interested persons are invited to send comments regarding this burden estimate or any other aspect of this collection of information, including any of the following subjects: (1) The necessity and utility of the

proposed information collection for the proper performance of the agency’s functions; (2) the accuracy of the estimated burden; (3) ways to enhance the quality, utility, and clarity of the information to be collected; and (4) the use of automated collection techniques or other forms of information

technology to minimize the information collection burden.

To obtain copies of the supporting

statement and any related forms for the

comments and recommendations for the proposed information collections must be directed to the OS Paperwork Clearance Officer at the above e-mail address within 60-days.

Proposed Project: Patient Centered Care Collaboration to Improve Minority Health, OMB# 0990–New, Office of Minority Health.

Abstract: The Office of Minority Health (OMH) in the Office of the Assistant Secretary for Health (OASH), Office of the Secretary (OS) is requesting approval from the Office of Management and Budget (OMB) for new data collection activities for the Patient Centered Care Collaboration to Improve Minority Health project (PCCC). This dissemination and adoption initiative funded in 2010, under the ARRA, 2009, through the Office of Minority Health and the Agency for Health Care Quality supports dissemination and adoption priorities as outlined in the HHS Report to Congress on Comparative Effectiveness Research. The PCCC evaluation will assess whether disseminating a diabetes education intervention in a community based health clinic and offering a medication management and adherence

intervention through home visits to seniors, improves the health and well being of racial and ethnic minority


ESTIMATED ANNUALIZED BURDEN TABLE

behaviors to improve their health status; and to determine if participants learned new information and skills that would help them to manage their health conditions and improve their health status.

Primary data for the evaluation will come from two waves of in person data collection from patients in a community health center in Chicago, Illinois and patients living in public housing in Houston, Texas. Data will be collected through a baseline survey at beginning

of intervention, and a follow up survey at approximately three months post- baseline in the two sites. Data collection for the entire evaluation is expected to last 6 months, from the time the first participant is enrolled until the last 4 month follow up survey is

administered.

The funding for this request is derived from American Reinvestment and Recovery Act of 2009 with hard and

non-negotiable deadlines for expenditures and completion. The end date for completion of all activities funded under this initiative is June 12,

2012. Thus, a rapid approval of OMB is requested, or the benefits of this initiative cannot be evaluated and HHS would not be able to report the benefits and outcome to the Congress as required.



Forms


Type of respondent


Number of respondents

Number of responses per respondent

Average burden (in hours) per response


Total burden hours

Chicago


Screening Questionnaire .................................. Intake Questionnaire ......................................... Post Questionnaire ...........................................


Sub-Total ...................................................

Individuals ......... Individuals ........ Individuals ........

165

50

40

1

1

1

5/60

40/60

40/60

14

33

27

...........................

255

1

............................

74

Houston


Eligibility Screening Form: Hypertension and

Diabetes.

First Home Visit Forms: Hypertension, Diabe- tes, or Hypertension and Diabetes.

Telephone Follow-up: Being Active and Man- aging Stress.

Telephone Follow-up: Healthy Eating ............... Post Intervention Follow-up Form: Hyper-

tension, Diabetes, or Hypertension and Dia-

betes.


Sub-total .....................................................

Individual .......... Individual .......... Individual ..........

Individual .......... Individual ..........

200


200


180


180

180

1


1


1


1

1

15/60


40/60


20/60


20/60

20/60

50


133


60


60

60

...........................

940

............................

............................

363

Shape4 Federal Register / Vol. 76, No. 185 / Friday, September 23, 2011 / Notices


ESTIMATED ANNUALIZED BURDEN TABLE—Continued

59131



Forms


Type of respondent


Number of respondents

Number of responses per respondent

Average burden (in hours) per response


Total burden hours

Total ....................................................

Individual ..........

1195

............................

............................

437



Keith Tucker,

Office of the Secretary, Paperwork Reduction

Act Clearance Officer.

[FR Doc. 2011–24442 Filed 9–22–11; 8:45 am]

BILLING CODE 4150–29–P

technology to minimize the information collection burden.

To obtain copies of the supporting

statement and any related forms for the proposed paperwork collections

infrastructure projects such as the MPCD. Within HHS, ASPE was tasked with managing the MPCD project in partnership with the Center for

Medicare and Medicaid Services (CMS).

referenced above, e-mail your request,

including your address, phone number,

The project represents a private/

public partnership with the goal of

DEPARTMENT OF HEALTH AND

HUMAN SERVICES


Agency Information Collection Request; 60-Day Public Comment Request


AGENCY: Office of the Assistant Secretary for Planning and Evaluation, Office of the Secretary, HHS.

In compliance with the requirement of section 3506(c)(2)(A) of the Paperwork Reduction Act of 1995, the

Office of the Secretary (OS), Department of Health and Human Services, is publishing the following summary of a proposed information collection request for public comment. Interested persons are invited to send comments regarding this burden estimate or any other aspect of this collection of information, including any of the following subjects: (1) The necessity and utility of the proposed information collection for the proper performance of the agency’s functions; (2) the accuracy of the estimated burden; (3) ways to enhance the quality, utility, and clarity of the information to be collected; and (4) the use of automated collection techniques or other forms of information

OMB number, and OS document

identifier, to [email protected], or call the Reports Clearance Office on (202)

690–6162. Written comments and recommendations for the proposed information collections must be directed to the OS Paperwork Clearance Officer

at the above e-mail address within 60 days.

Proposed Project: Multi-Payor Claims

Database (New—XXXXXXX).

Office of the Assistant Secretary for

Planning and Evaluation (ASPE)— American Recovery and Reinvestment Act-funded Comparative Effectiveness Research Program.

Abstract

The Multi-Payor Claims Database (MPCD) project is one of a number of initiatives related to comparative effectiveness research (CER) funded by the American Recovery and Reinvestment Act of 2009. The Act provided $1.1 billion to build the necessary infrastructure and capacity to support CER. Approximately 25% of the

$400 million allocated to the Office of the Secretary for Health and Human Services went towards data


ESTIMATED ANNUALIZED BURDEN TABLE

consolidating access to longitudinal

data on health services financed by both public and private payers to help facilitate CER. Inclusion of data from multiple sources should allow for adequate coverage of priority patient populations, less common medical conditions, health care interventions, and geographic areas. As the title of the project suggests, the MPCD will initially include claims data, since these data are most readily available. Over time, data with additional clinical detail from

other sources, such as EHRs, may be incorporated into the database.

The contract to develop the MPCD is

a 3-year contract between Ingenix Public Sector Solutions (as the primary contractor) and ASPE. We envision several types of respondents, accessing data at different tiers within the MPCD, as shown in the table below. The respondents will not be accessing data

on any regular frequency, but rather on an ad hoc basis. The affected public will be individual researchers, health policy analysts and researchers at affiliated with MPCD data contributors as well as key stakeholder staff and analysts

within HHS.



Forms


Type of respondent


Number of respondents

Number of responses per respondent

Average bur- den (in hours) per response


Total burden hours

Tiers 1, 2 and 3 .......................... Tiers 1 and 2 .............................. Tier 1 ..........................................

Total ....................................

Principal Investigators, Project Data An- alysts and Project Directors.

Healthcare Organization administrators and analysts.

Patients and consumers .........................


.................................................................

293


125


50

3


3


4

35/60


20/60


5/60

513


125


17

........................

........................

........................

655



Office of Minority Health Patient Centered Care Collaboration Initiative

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