Agency Information Collection Activities; Proposals, Submissions, and Approvals

Federal Register: March 14, 2008 (Volume 73, Number 51)

Notices

Page 13900-13901

From the Federal Register Online via GPO Access [wais.access.gpo.gov]

DOCID:fr14mr08-73

DEPARTMENT OF HEALTH AND HUMAN SERVICES

Agency for Healthcare Research and Quality

Agency Information Collection Activities: Proposed Collection;

Comment Request

AGENCY: Agency for Healthcare Research and Quality, HHS.

ACTION: Notice.

SUMMARY: This notice announces the intention of the Agency for

Healthcare Research and Quality (AHRQ) to request that the Office of

Management and Budget (OMB) approve the proposed information collection project: ``Focus Groups on Consumer Engagement in Developing Electronic

Health Information Systems.'' In accordance with the Paperwork

Reduction Act of 1995, (44 U.S.C. 3506(c)(2)(A)), AHRQ invites the public to comment on this proposed information collection.

This proposed information collection was previously published in the Federal Register on December 28th, 2007 and allowed 60 days for public comment. Comments were received. The purpose of this notice is to allow an additional 30 days for public comment.

DATES: Comments on this notice must be received by May 13, 2008.

ADDRESSES: Written comments should be submitted to: Doris Lefkowitz,

Reports Clearance Officer, AHRQ, by e-mail at doris.lefkowitz@ahrq.hhs.gov.

Copies of the proposed collection plans, data collection instruments, and specific details on the estimated burden can be obtained from the AHRQ Reports Clearance Officer.

FOR FURTHER INFORMATION CONTACT: Doris Lefkowitz, AHRQ Reports

Clearance Officer, (301) 427-1477, or by email at doris.letkowitz@ahrq.hhs.gov.

SUPPLEMENTARY INFORMATION:

Proposed Project: ``Focus Groups on Consumer Engagement in Developing

Electronic Health Information Systems''

This project will consist of focus groups to gain insights into healthcare consumers' awareness and perceptions of Health Information

Technology (IT), and how best to engage consumers in the development of these technologies. AHRQ has so far invested significant resources in initiatives to promote the planning and development of new Health IT that should improve healthcare, lower healthcare costs, and improve patient safety. For such benefits to be maximized, it is important to understand how consumers view Heath IT and how to engage them in the design and implementation of future innovations.

AHRQ will conduct 20 focus groups (in addition to two pretest groups) with healthcare consumers, that is persons who have visited a healthcare provider (either for their own health or the health of a family member) in the previous two years. For the most part, the groups will be homogenous with respect to the presence or absence of either of the following characteristics: (a) Managing a chronic health condition

(or the condition of a close family member), or (b) Having visited at least three healthcare providers in the past two years.

Participants will be covered by a range of health insurance plans, and persons not covered by health insurance will also be recruited.

Some groups will include only persons 2 enrolled in a Health Maintaince

Organization (HMO).

The data to be collected for this project will be in two form a) answers to a screener questionnaire designed to identify and recruit eligible participants, and b) verbal reports--i.e., focus group participants' answers to questions posed by the moderator and reactions to comments of other group members. The focus group discussions will be audio-taped with participants' consent and transcribed for analysis purposes.

Method of Collection

Participants will be screened for eligibility and recruited for the focus groups by telephone. The focus group sessions will be conducted in-person with approximately 10 persons per group. The focus group discussion will take approximately 2 hours, and we have assumed a 20- minute travel time (each way) per participant. Thus, focus group participation will require 2.67 hours per response. Estimated Annual

Respondent Burden

Page 13901

Table 1.--Estimated annualized burden hours

Number of

Form name

Number of

responses per

Hours per

Total burden respondents

respondent

response

hours

Recruiting Screener Focus Group Discussion......

2,200

1

5/60

183

Guide...........................................

220

1

2.67

587

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

2,420

na

na

770

Table 2.--Estimated annualized cost burden

Number of

Total burden Average hourly

Total cost

Form name

respondents

hours

wage rate*

burden

Recruiting Screener Focus Group Discussion......

2,200

183

$17

3,111

Guide...........................................

220

587

17

9,979

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

2,420

770

na

13,090

* Based upon the mean hourly wage of full-time workers, third-quarter of 2007. Current Population Survey, U.S.

Department of Labor, Bureau of Labor Statistics.

Estimated Annual Costs to the Federal Government

Based on the current budget for the project, the total cost to the

Federal Government is $257,474 ($251, 114 of contractor costs + $6,360 of travel and time cost for AHRQ employees) for the 18-month period from Oct. 1st, 2007 to March 31st, 2009. The annualized cost is approximately $171,649. This amount includes all direct and indirect costs of the design, data collection, analysis, and reporting phases of the study. The costs of Federal employees for monitoring the contract are $5,660.

Request for Comments

In accordance with the above-cited Paperwork Reduction Act legislation, comments on AHRQ's information collection are requested with regard to any of the following: (a) Whether the proposed collection of information is necessary for the proper performance of

AHRQ health care research and health care information dissemination functions, including whether the information will have practical utility; (b) the accuracy of AHRQ's estimate of burden (including hours and costs) of the proposed collection(s) 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 upon the respondents, including the use of automated collection techniques or other forms of information technology.

Comments submitted in response to this notice will be summarized and included in the Agency's subsequent request for OMB approval of the proposed information collection.

All comments will become a matter of public record.

Dated: March 5, 2008.

Carolyn M. Clancy,

Director.

FR Doc. E8-4928 Filed 3-13-08; 8:45 am

BILLING CODE 4160-90-M

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