Form #4 Pre-Focus Group Questionnaire - Group2

Generic Clearance for the Collection of Qualitative Feedback on Agency Service Delivery

Attachment C2 -- Pre-Focus Group Questionnaire Group2

Customer Satisfaction with AHRQ's Patient-Centered Outcomes Research (PCOR) Educational Materials

OMB: 0935-0179

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Form Approved
OMB No. 0935-0179
Exp. Date 7/31/2014



ATTACHMENT C2

Pre-Focus Group Questionnaire (Group 2)

Definition: Shared decision-making is a process where both the patient and clinician share information, participate in the decisionmaking process, and agree on the best strategy for treatment. The clinician provides personalized information, tools, and/or decision aids to help the patient understand available treatment options, and encourages the patient to consider his or her personal values in making treatment-related decisions.



  1. Keeping in mind the definition of shared decisionmaking above, how often would you say you involve your patients in the decisionmaking process regarding their care in each of the following situations?



Every time

Almost every time

Occasionally

Almost never

Never

Changing their lifestyle behaviors

Deciding on their medicines (e.g., blood pressure, cholesterol, depression)

Whether or not to undergo cancer screening tests (e.g., colon, breast, prostate)

Having surgery (e.g., back surgery, knee or hip replacements)

Choosing between various cardiac procedures

Managing chronic conditions

Having an MRI or CT Scan



  1. When the subject of medical treatments, procedures, or medicine regime comes up, how much time per visit are you able to spend with individual patients discussing options or in decisionmaking processes?


    • 3 minutes or less

    • 4 to 5 minutes

    • 6 to 10 minutes

    • 11 to 15 minutes

    • More than 15 minutes





Public reporting burden for this collection of information is estimated to average 2 minutes per response, the estimated time required to complete the survey. An agency may not conduct or sponsor, and a person is not required to respond to, a collection of information unless it displays a currently valid OMB control number. Send comments regarding this burden estimate or any other aspect of this collection of information, including suggestions for reducing this burden, to: AHRQ Reports Clearance Officer Attention: PRA, Paperwork Reduction Project (0935-XXXX) AHRQ, 540 Gaither Road, Room # 5036, Rockville, MD 20850.











  1. To what extent have you found that the following situations prohibit you from fully engaging patients as much as you would like in the decisionmaking process or educating about the patient’s health care options?



To a great extent

Somewhat

Not at all

Not having enough time with patients

Not having access to trusted sources of information that can be used in this process

Not being able to stay up-to-date on current clinical research

Patients/caregivers having difficulty understanding the information

Patients not being interested in participating in this process

Patients not being confident in participating in this process

Coming from a different culture

Not speaking the same language

Other reasons (Please specify other reasons) ________________________________________


  1. When you engage in shared decision making with patients, how do you do it (please select all that apply)?


  • At the point of care, through one-on-one conversations with the patient

  • At the point of care with family or other caregivers present

  • By phone before their visit

  • Directing patients to a Web site that provides patient decision aids online prior to their visit

  • Directing patients to a Web site that provides patient decision aids online after their visit

  • In a group setting

  • Some other way (please specify)__________________


  1. How valuable would you find each of the following topics in a training course on educating patients about their health care options:



Very valuable

Somewhat valuable

Not very valuable

Not valuable at all

How to communicate technical information about health care options with patients

How to discuss harms and benefits of various health care options

How to address different cultural sensitivities of my patients

How to convey information to patients with who speak little English

How to convey information about likely outcomes of different health care options

How to engage patients to better understand their preferences and values

Where I can find and access information that would be useful to me in my practice

Other topics that would be valuable (Please specify)_____________________


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AuthorLola Oguntomilade
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File Modified2013-05-17
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