[Federal Register Volume 75, Number 73 (Friday, April 16, 2010)]
[Notices]
[Pages 19978-19979]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2010-8800]
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DEPARTMENT OF HEALTH AND HUMAN SERVICES
National Institutes of Health
Proposed Collection; Comment Request; Web Based Training for Pain
Management Providers
SUMMARY: Under the provisions of Section 3507(a)(1)(D) of the Paperwork
Reduction Act of 1995, the National Institute on Drug Abuse, the
National Institutes of Health has submitted to the Office of Management
and Budget (OMB) a request to review and approve the information
collection listed below. This proposed information collection was
previously published in the Federal Register in Vol. 75, No. 25 on
Monday, February 8 and allowed 60 days for public comment. No public
comments were received on the planned study or any of the specific
topics outlined in the 60 day notice. Three comments were received
requesting information on the educational program rather than the
study. We responded to requests for additional information from
interested parties. The purpose of this notice is to allow an
additional 30 days for public comment.
5 CFR 1320.5 (General requirements) Reporting and Recordkeeping
Requirements: Final Rule requires that the agency inform the potential
persons who are to respond to the collection of information that such
persons are not required to respond to the collection of information
unless it displays a currently valid OMB control number.
Proposed Collection
Title: Web Based Training for Pain Management Providers.
Type of Information Collection Request: New.
Need and Use of Information Collection: This research will evaluate
the effectiveness of the Web Based Training for Pain Management
Providers, via the Web site PainAndAddictionTreatment.com, to
positively impact the knowledge, attitudes, intended behaviors and
clinical skills of health care providers in the U.S. who treat pain.
The Web Based Training for Pain Management Providers is a new program
developed with funding from the National Institute on Drug Abuse. The
primary goal is to assess the impact of the training program on
knowledge, attitude, intended behavior, and clinical skills. A
secondary goal is to assess learner satisfaction with the program. If
the program is a success, there will be a new, proven resource
available to health care providers to improve their ability to treat
pain and addiction co-occurring in the provider's patients. In order to
evaluate the effectives of the program, information will be collected
from health care providers before exposure to the Web based materials
(pre-test), after exposure to the web based materials (post-test), and
4-6 weeks after the program has been completed (follow-up).
Frequency of Response: On occasion.
Affected Public: Volunteer health care providers who treat patients
with pain.
Type of Respondents: Physicians, nurse practitioners, and physician
assistants.
The annual reporting burden is as follows:
Estimated Number of Respondents: 80.
Estimated Number of Responses per Respondent: 3.
Average Burden Hours per Response: 0.75.
Estimated Total Annual Burden Hours Requested: 180.
The annualized cost to respondents is estimated at: $11,925. There
are no Capital Costs, Operating Costs, and/or Maintenance Costs to
report.
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Estimated Estimated
Estimated number of Average burden annual burden
Type of respondents number of responses per hours per hours
respondents respondent response requested
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Physicians...................................... 60 3 0.75 135
[[Page 19979]]
Other primary care providers (e.g., nurse 20 3 0.75 45
practitioners, physician assistants)...........
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Request for Comments: Written comments and/or suggestions from the
public and affected agencies are invited on one or more of the
following points: (1) Whether the proposed collection of information is
necessary for the proper performance of the function of the agency,
including whether the information will have practical utility; (2) The
accuracy of the agency's estimate of the burden of the proposed
collection of information, including the validity of the methodology
and assumptions used; (3) Ways to enhance the quality, utility, and
clarity of the information to be collected; and (4) Ways to minimize
the burden of the collection of information on those who are to
respond, including the use of appropriate automated, electronic,
mechanical, or other technological collection techniques or other forms
of information technology.
Direct Comments to OMB: Written comments and/or suggestions
regarding the item(s) contained in this notice, especially regarding
the estimated public burden and associated response time, should be
directed to the: Office of Management and Budget, Office of Regulatory
Affairs, [email protected] or by fax to 202-395-6974,
Attention: Desk Officer for NIH. To request more information on the
proposed project or to obtain a copy of the data collection plans and
instruments, contact: Scudder Quandra, Project Officer, NIH/NIDA/CCTN,
Room 3105, MSC 9557, 6001 Executive Boulevard, Bethesda, MD 20892-9557
or e-mail your request, including your address to
[email protected].
Comments Due Date: Comments regarding this information collection
are best assured of having their full effect if received within 30 days
of the date of this publication.
Dated: April 8, 2010.
Mary Affeldt,
Executive Officer (OM Director), NIDA, National Institutes of Health.
[FR Doc. 2010-8800 Filed 4-15-10; 8:45 am]
BILLING CODE 4140-01-P