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Agency Information Collection Activities: Submission to OMB for Review and Approval; Public Comment Request

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AGENCY:

Health Resources and Services Administration, HHS.

ACTION:

Notice.

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SUMMARY:

In compliance with Section 3507(a)(1)(D) of the Paperwork Reduction Act of 1995, the Health Resources and Services Administration (HRSA) has submitted an Information Collection Request (ICR) to the Office of Management and Budget (OMB) for review and approval. Comments submitted during the first public review of this ICR will be provided to OMB. OMB will accept further comments from the public during the review and approval period.

DATES:

Comments on this ICR should be received within 30 days of this notice.

ADDRESSES:

Submit your comments, including the Information Collection Request Title, to the desk officer for HRSA, either by email to OIRA_submission@omb.eop.gov or by fax to 202-395-5806.

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FOR FURTHER INFORMATION CONTACT:

To request a copy of the clearance requests submitted to OMB for review, email the HRSA Information Collection Clearance Officer at paperwork@hrsa.gov or call (301) 443-1984.

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SUPPLEMENTARY INFORMATION:

Information Collection Request Title: Questionnaire and Data Collection Testing, Evaluation, and Research for the Health Resources and Services Administration.

OMB No.: 0915-xxxx—New.

Abstrac t: The purpose of collections under this generic clearance is to obtain formative information from respondents to develop new questions, questionnaires, and tools and to identify problems in instruments currently in use. This clearance request is limited to formative research activities emphasizing data collection, toolkit development, and estimation procedures and reports for internal decision-making and development purposes; and does not extend to the collection of data for public release or policy formation.

It is anticipated that these studies will rely heavily on qualitative techniques to meet their objective. In general, these activities are not designed to yield results that meet generally accepted standards of statistical rigor; rather, these activities are designed to obtain valuable formative information to develop more effective and efficient data collection tools that will yield more accurate results and decrease non-response.

HRSA conducts cognitive interviews, focus groups, usability tests, field tests/pilot interviews, and experimental research in laboratory and field settings, both for applied questionnaire development and evaluation, as well as more basic research on response errors in surveys.HRSA staff use various techniques to evaluate interviewer administered, self-administered, telephone, Computer Assisted Personal Interviewing (CAPI), Computer Assisted Self-Interviewing (CASI), Audio Computer-Assisted Self-Interviewing (ACASI), and web-based questionnaires.

Professionally recognized procedures will be followed in each information collection activity to ensure high quality data. Examples of these procedures are likely to include:

  • A certain percent of telephone interviews will be monitored by supervisory staff of a certain percent of telephone interviews;
  • Cognitive interviewing techniques will be conducted, including think-aloud techniques and debriefings;
  • Data-entry from mail or paper-and-pencil surveys will be computerized through scannable forms or checked through double-key entry;
  • Observers will monitor focus groups, and focus group proceedings will be recorded; and
  • Data submitted through on-line surveys will be subjected to statistical validation techniques to ensure accuracy (such as disallowing out-of-range values).

Each request under this generic clearance will specify the procedures to be used. Participation will be fully voluntary, and non-participation will not affect eligibility for, or receipt of, future HRSA health services research activities, grant awards, recruitment, or participation. Specific testing and evaluation procedures will be described when we notify OMB about each new request. Consent procedures will be customized for each information collection activity, but will include assurances of confidentiality and the legislative authority for the activity. If the encounter is to be recorded, the respondent's permission to record will be obtained before beginning the interview.

Recruitment—Respondents will be recruited by means of advertisements in public venues or through techniques that replicate prospective data collection activities that are the focus of the project. For instance, a survey on physician communication, designed to be administered following an office visit, might be pretested using the same procedure. Each submission to OMB will specify the specific recruitment procedure to be used.

Screening—When screening is required (e.g., quota sampling), the screening will be as brief as possible, and the screening questionnaire will be provided as part of the submission to OMB.

Collection methods—The particular information collection methods used will vary, but may include the following:

  • Individual in-depth interviews—In-depth interviews will commonly be used to ensure that the meaning of a questionnaire or strategy is understood by the respondent. When in-depth interviewing is used, the interview guide will be provided to OMB for review.
  • Focus groups—Focus groups will be used to obtain insights into beliefs and understandings of the target audience early in the development of a questionnaire or tool. When focus groups are used, the focus group discussion guide will be provided to OMB for review.
  • Expert/Gatekeeper review of tools—In some instances, tools designed for patients may be reviewed in-depth by medical providers or other gatekeepers to provide feedback on the acceptability and usability of a particular tool. This would usually be in addition to pretesting of the tool by the actual patient or other user.
  • Record abstractions—On occasion, the development of a tool or other information collection requires review and interaction with records rather than individuals.
  • “Dress rehearsal” of a specific protocol—In some instances, the proposed pretesting will constitute a walkthrough of the intended data collection procedure. In these instances, the request will mirror what is expected to occur for the larger scale data collection.

Burden Statement: Burden in this context means the time expended by persons to generate, maintain, retain, disclose or provide the information requested. This includes the time needed to review instructions; to develop, acquire, install and utilize technology and systems for the purpose of collecting, validating and verifying information, processing and maintaining information, and disclosing and providing information; to train personnel and to be able to respond to a collection of information; to search data sources; to complete and review the collection of information; and to transmit or otherwise disclose the information. The total annual burden hours estimated for this Information Collection Request are summarized in the table below.Start Printed Page 8199

Total Estimated Annualized Burden Hours

Type of information collectionNumber of respondentsNumber of responses per respondentTotal responsesAverage burden per response (in hours)Total burden hours
Mail/email 110,000110,0000.55,000
Telephone10,000110,0000.55,000
Web-based10,000110,0000.55,000
Focus Groups10,000110,0002.020,000
In-person10,000110,0001.010,000
Automated 210,000110,0001.010,000
Cognitive Interviewing30,000130,0002.060,000
Total90,00090,000115,000
1 May include telephone non-response follow-up in which case the burden will not change.
2 May include testing of database software, CAPI software, or other automated technologies.
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Dated: February 5, 2014.

Bahar Niakan,

Director, Division of Policy and Information Coordination.

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[FR Doc. 2014-02896 Filed 2-10-14; 8:45 am]

BILLING CODE 4165-15-P