Federal Register: November 26, 2008 (Volume 73, Number 229)
DOCID: fr26no08-86 FR Doc E8-28048
DEPARTMENT OF HEALTH AND HUMAN SERVICES
Health Resources and Services Administration
NOTICE: NOTICES
DOCID: fr26no08-86
SUBJECT CATEGORY:
Agency Information Collection Activities: Proposed Collection: Comment Request
DOCUMENT SUMMARY:
In compliance with the requirement for opportunity for public comment on proposed data collection projects (section 3506(c)(2)(A) of Title 44, United States Code, as amended by the Paperwork Reduction Act of 1995, Pub. L. 10413), the Health Resources and Services Administration (HRSA) publishes periodic summaries of proposed projects being developed for submission to the Office of Management and Budget (OMB) under the Paperwork Reduction Act of 1995. To request more information on the proposed project or to obtain a copy of the data collection plans and draft instruments, email paperwork@hrsa.gov or call the HRSA Reports Clearance Officer on (301) 4431129.
Comments are invited on: (a) The proposed collection of information
for the proper performance of the functions of the agency; (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: Patient Navigator Outreach and Chronic Disease
Prevention Demonstration Program Patient Data Collection FormNEW
The purpose of the Patient Navigator Outreach and Chronic Disease Prevention (PN) Demonstration Program is to promote model ``patient navigator'' programs to improve health care outcomes for individuals with cancer and/or other chronic diseases, with a specific emphasis on health disparity populations. This program aims to coordinate comprehensive health services for patients in need of chronic disease care and management through enhanced chronic disease management provided by patient navigators.
In order to describe successful PN program models and make
recommendations on the ability of such programs to improve patient
outcomes, data is needed at the individual patient, patient navigator, and PN program levels. This information includes:
This information will be collected from patients or their designated caregiver, patient navigators, and PN program
administrators. Maintaining confidentiality of patient medical
information is a concern and thus all personal information will be de
identified to protect the confidentiality of all patients. Data
collection and disclosure processes will abide by Health Insurance
Portability and Accountability Act (HIPPA) Privacy Rule provisions and procedures. The estimated annual burden is as follows:
Number of Responses per Total Hours per Total burden
Form respondents respondent responses response hours
Navigated Patient \1\ Data 6,000 1 6,000 0.5 3,000 Intake Form....................
Navigated Patient Satisfaction 6,000 1 6,000 0.25 1,500 Survey.........................
SubTotalPatient Burden.... 6,000 2 1,2000 0.75 4,500
Patient Navigator Survey........ 30 1 30 0.25 7.5
Patient Navigator Encounter/ 30 750 22,500 0.25 5,625 Tracking Log \2\...............
SubTotalPatient Navigator 30 751 22,530 0.5 5,632.5 Burden.....................
Grantee PN Administrative 6 1 6 0.5 3 Records \3\....................
Medical Record and Clinic Data 6 2,000 12,000 2 24,000 \4\............................
SubTotalGrantee Burden.... 12 2,001 12,012 2.5 24,006
===============================================================================
Total Average Annual 6,052 2,754 54,052 3.75 36,016 Burden.................
\1\ Estimated number of navigated patients per year based on applications was rounded to 6000. See table below for projected numbers navigated by Grantee.
\2\ Assumes 5 log entries of PN activities per patient.
[[Page 72065]]
\3\ Includes administrative data related to PN recruitment, hiring, and training.
\4\ Includes medical record abstraction and clinic database abstraction on individual patients (note: decreased to 2 hours per patient).
Over 2
yrs Annual
Goodwin........................................... 400 200
Lutheran.......................................... 650 325
Northeast......................................... 6,000 3,000
Palmetto.......................................... 3,000 1,500
South Broward..................................... 2,200 1,100
Texas Tech........................................ 500 250
Total......................................... 12,750 6,375
Email comments to paperwork@hrsa.gov or mail the HRSA Reports
Clearance Officer, Room 1033, Parklawn Building, 5600 Fishers Lane,
Rockville, MD 20857. Written comments should be received within 60 days of this notice.
Dated: November 20, 2008.
Alexandra Huttinger,
Director, Division of Policy Review and Coordination.
[FR Doc. E828048 Filed 112508; 8:45 am]
BILLING CODE 416515P
SUMMARY:
Agency Information Collection Activities; Proposals, Submissions, and Approvals,
DOCUMENT BODY 2:
In compliance with the requirement for opportunity for public comment on proposed data collection projects (section 3506(c)(2)(A) of Title 44, United States Code, as amended by the Paperwork Reduction Act of 1995, Pub. L. 10413), the Health Resources and Services Administration (HRSA) publishes periodic summaries of proposed projects being developed for submission to the Office of Management and Budget (OMB) under the Paperwork Reduction Act of 1995. To request more information on the proposed project or to obtain a copy of the data collection plans and draft instruments, email paperwork@hrsa.gov or call the HRSA Reports Clearance Officer on (301) 4431129.
Comments are invited on: (a) The proposed collection of information
for the proper performance of the functions of the agency; (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: Patient Navigator Outreach and Chronic Disease
Prevention Demonstration Program Patient Data Collection FormNEW
The purpose of the Patient Navigator Outreach and Chronic Disease Prevention (PN) Demonstration Program is to promote model ``patient navigator'' programs to improve health care outcomes for individuals with cancer and/or other chronic diseases, with a specific emphasis on health disparity populations. This program aims to coordinate comprehensive health services for patients in need of chronic disease care and management through enhanced chronic disease management provided by patient navigators.
In order to describe successful PN program models and make
recommendations on the ability of such programs to improve patient
outcomes, data is needed at the individual patient, patient navigator, and PN program levels. This information includes:
This information will be collected from patients or their designated caregiver, patient navigators, and PN program
administrators. Maintaining confidentiality of patient medical
information is a concern and thus all personal information will be de
identified to protect the confidentiality of all patients. Data
collection and disclosure processes will abide by Health Insurance
Portability and Accountability Act (HIPPA) Privacy Rule provisions and procedures. The estimated annual burden is as follows:
Number of Responses per Total Hours per Total burden
Form respondents respondent responses response hours
Navigated Patient \1\ Data 6,000 1 6,000 0.5 3,000 Intake Form....................
Navigated Patient Satisfaction 6,000 1 6,000 0.25 1,500 Survey.........................
SubTotalPatient Burden.... 6,000 2 1,2000 0.75 4,500
Patient Navigator Survey........ 30 1 30 0.25 7.5
Patient Navigator Encounter/ 30 750 22,500 0.25 5,625 Tracking Log \2\...............
SubTotalPatient Navigator 30 751 22,530 0.5 5,632.5 Burden.....................
Grantee PN Administrative 6 1 6 0.5 3 Records \3\....................
Medical Record and Clinic Data 6 2,000 12,000 2 24,000 \4\............................
SubTotalGrantee Burden.... 12 2,001 12,012 2.5 24,006
===============================================================================
Total Average Annual 6,052 2,754 54,052 3.75 36,016 Burden.................
\1\ Estimated number of navigated patients per year based on applications was rounded to 6000. See table below for projected numbers navigated by Grantee.
\2\ Assumes 5 log entries of PN activities per patient.
[[Page 72065]]
\3\ Includes administrative data related to PN recruitment, hiring, and training.
\4\ Includes medical record abstraction and clinic database abstraction on individual patients (note: decreased to 2 hours per patient).
Over 2
yrs Annual
Goodwin........................................... 400 200
Lutheran.......................................... 650 325
Northeast......................................... 6,000 3,000
Palmetto.......................................... 3,000 1,500
South Broward..................................... 2,200 1,100
Texas Tech........................................ 500 250
Total......................................... 12,750 6,375
Email comments to paperwork@hrsa.gov or mail the HRSA Reports
Clearance Officer, Room 1033, Parklawn Building, 5600 Fishers Lane,
Rockville, MD 20857. Written comments should be received within 60 days of this notice.
Dated: November 20, 2008.
Alexandra Huttinger,
Director, Division of Policy Review and Coordination.
[FR Doc. E828048 Filed 112508; 8:45 am]
BILLING CODE 416515P