Request for Approval under the “Generic Clearance for the Collection of Routine Customer Feedback” (OMB Control Number: 0920-105

CDC DHQP_CDIFF IDI Gen IC Request Form_HCPs_4.12.24_Final.docx

[OS] CDC/ATSDR Formative Research and Tool Development

Request for Approval under the “Generic Clearance for the Collection of Routine Customer Feedback” (OMB Control Number: 0920-105

OMB: 0920-1154

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Request for genIC Approval

CDC/ATSDR Formative Research and Tool Development

0920-1154



CIO: National Center for Emerging and Zoonotic Infectious Diseases

PROJECT TITLE: In-Depth Interviews with Healthcare Professionals about C. Diff Materials

PURPOSE AND USE OF COLLECTION: The Centers for Disease Control and Prevention (CDC) is requesting approval for a new generic information collection (gen-IC). The goals of this evaluation are to test a set of draft C. diff communications materials among healthcare professionals (HCPs) to ensure materials effectively communicate information about C. diff risks, answer questions about C. diff risk factors, and are useful in assessing patient risk for C. diff and discussing it with patients.

DESCRIPTION OF RESPONDENTS: Dentists, physicians, physician associates/assistants (PAs), and nurse practitioners (NPs) in dental, primary care, urgent care, hospital, and emergency department settings.

CERTIFICATION:

I certify the following to be true:

  1. The collection is voluntary.

  2. The collection is low-burden for respondents and low-cost for the Federal Government.

  3. The collection is non-controversial and does not raise issues of concern to other federal agencies.

  4. Information gathered will not be used to substantially inform influential policy decisions.

  5. The study is not intended to produce results that can be generalized beyond its scope.

Name: Mike Ruddell, Vice President, KRC Research

To assist review, please answer the following questions:

Personally Identifiable Information:

  1. Is personally identifiable information (PII) collected? [X] Yes [ ] No

  2. If Yes, is the information that will be collected included in records that are subject to the Privacy Act of 1974? [ ] Yes [X] No

  3. If Applicable, has a System or Records Notice been published? [ ] Yes [X] No



Gifts or Payments:

Is an incentive (e.g., money or reimbursement of expenses, token of appreciation) provided to participants? [X] Yes [ ] No



Focus group participants will receive a monetary incentive of $75 for their participation. Such an incentive is a standard practice in the market research industry and helps to ensure efficient recruitment and ultimate participation among the qualified and scheduled participants. The incentive is also intended to offset the cost of personal or professional time taken to participate.

BURDEN HOURS

Form Name

Type of Respondent

No. of Respondents

No. of Responses per Respondent

Average Burden Per Response (hours)

Total Burden Hours

Screener for C. diff Materials Testing Interviews (Attachment 1)

Dentist

20

1

5/60

2

Primary care physician

10

1

5/60

1

Primary care NP or PA

10

1

1

1

Urgent care physician

10

1

5/60

1

Urgent care NP or PA

10

1

5/60

1

Emergency physician

10

1

5/60

1

Emergency NP or PA

10

1

5/60

1

Hospitalist physician

30

1

5/60

3

Discussion Guide for C. diff Materials Testing Interviews

(Attachment 3)

Dentist

2

1

1

2

Primary care physician

1

1

1

1

Primary care NP or PA

1

1

1

1

Urgent care physician

1

1

1

1

Urgent care NP or PA

1

1

1

1

Emergency physician

1

1

1

1

Emergency NP or PA

1

1

1

1

Hospitalist physician

3

1

1

3

Total


22


FEDERAL COST: The estimated annual cost to the Federal government is $30,614,94.

If you are conducting a focus group, survey, or plan to employ statistical methods, please provide answers to the following questions:

The selection of your targeted respondents

  1. Do you have a customer list or something similar that defines the universe of potential respondents and do you have a sampling plan for selecting from this universe? [X] Yes [ ] No

If the answer is yes, please provide a description of both below (or attach the sampling plan)? If the answer is no, please provide a description of how you plan to identify your potential group of respondents and how you will select them?

Potential participants are drawn from a national panel of individuals who have opted in to participate in interviews on various topics. The contractor KRC Research will direct a vendor panel provider to distribute an invitation to screen for the interviews to members of its panel, starting with those individuals whose panel profiles suggest they are most likely to qualify (e.g., known to be physicians or NPs or PAs, have known specialties). When an individual receives the invitation to screen, they will either complete a screening questionnaire online (Attachment 1) or via the phone in a call with a panel provider staff member. Individuals must pass the screening questionnaire without being disqualified based on their answers or due to quotas reached on certain characteristics.

Eleven participants will be purposively selected from this pool of eligible participants for a total of 11 interviews. In addition to requirements about healthcare provider role and work setting, participants will also be selected to maximize variability across geographic region, age, sex, and race and ethnicity.

Administration of the Instrument

  1. How will you collect the information? (Check all that apply)

[X] Web-based or other forms of Social Media

[ ] Telephone

[ ] In-person

[ ] Mail

[ ] Other, Explain

  1. Will interviewers or facilitators be used? [X] Yes [ ] No

Please make sure all instruments, instructions, and scripts are submitted with the request.





Instructions for completing genIC Request for Approval for

CDC/ATSDR Formative Research and Tool Development



Shape1 TITLE OF INFORMATION COLLECTION: Provide the name of the collection that is requested.

PURPOSE and USE: Provide a brief description of the purpose of this collection and how it will be used. If this is part of a larger study or effort, please include this in your explanation.

DESCRIPTION OF RESPONDENTS: Briefly describe the targeted group/groups for this collection.

CERTIFICATION: Please read the certification carefully. If you incorrectly certify, the collection will be returned as improperly submitted or it will be disapproved.

Personally Identifiable Information: Provide answers to the questions.

Gifts or Payments: If you answer yes to the question, please describe the incentive and provide a justification for the amount.

BURDEN HOURS:

Category of Respondents: Identify who you expect the respondents to be in terms of the following categories: (1) Individuals or Households; (2) Private Sector; (3) State, local, or tribal governments; or (4) Federal Government. Only one type of respondent can be selected.

Form: Provide the title of the information collection form.

No. of Respondents: Provide an estimate of the Number of respondents.

Participation Time: Provide an estimate of the amount of time required for a respondent to participate (e.g. fill out a survey or participate in a focus group).

Burden in Minutes: Multiply the Number of responses and the participation time and divide by 60.

FEDERAL COST: Estimate the annual cost to the Federal government for this collection.

If you are conducting a focus group, survey, or plan to employ statistical methods, please provide answers to the following questions:

The selection of your targeted respondents. Please provide a description of how you plan to identify your potential group of respondents and how you will select them. If the answer is yes, to the first question, you may provide the sampling plan in an attachment.

Administration of the Instrument: Identify how the information will be collected. More than one box may be checked. Indicate whether there will be interviewers (e.g. for surveys) or facilitators (e.g., for focus groups) used.

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File TitleDOCUMENTATION FOR THE GENERIC CLEARANCE
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