| Please provide your feedback by completing this 10-15 min. survey. The CDC Office of Public Health Genomics will use this information to improve its resources. Your participation in this survey is completely voluntary and anonymous. |
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| If you have any questions or technical difficulties while taking the survey, please contact James O'Leary (joleary@geneticalliance.org). |
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| DEMOGRAPHICS |
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| 1 |
Question |
In what sector is your primary profession? |
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Answer (Multiple choice/multiple answers) |
(Choose all that apply) |
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Clinical Healthcare |
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State or Local Public Health Agency |
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Academia: Faculty / Researcher / Staff / Student |
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Federal Health Agency: CDC |
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Federal Health Agency: Other |
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Community Organization |
| 2 |
Question: |
What is your position/job title? |
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| 3 |
Question: |
Please provide the name of the State in which your primary physical work is found. |
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| Answer(Short Answer) |
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| AWARENESS |
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| 4 |
Question: |
BEFORE the webinar, which CDC Office of Public Health Genomics resource(s) were you aware of? Choose all that apply |
| Answer (Multiple Choice/Multiple Answers) |
Public Health Genomics Knowledge Base |
| Tier Table Database |
| Tier 1 Genomic Applications Toolkit for Public Health Departments |
| State Genomics Implementation Map |
| CDC Office of Public Health Genomics Website |
| None of the Above |
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| USAGE |
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| 5 |
Question: |
In the past 12 months, how often have you used the CDC Office of Public Health Genomics website? |
| Answer (Multiple Choice, One Answer) |
Daily |
| Weekly |
| Monthly |
| A few times per year |
| At least once per year |
| Never |
| Don't Know |
| Not Applicable/Not needed for my work |
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| 6 |
Question: |
In the past 12 months, how often have you used the Public Health Genomics Knowledge Base? |
| Answer (Multiple Choice, One Answer) |
Daily |
| Weekly |
| Monthly |
| A few times per year |
| At least once per year |
| Never |
| Don't Know |
| Not Applicable/Not needed for my work |
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| 7 |
Question: |
In the past 12 months, how often have you used the Tier Table Database? |
| Answer (Multiple Choice, One Answer) |
Daily |
| Weekly |
| Monthly |
| A few times per year |
| At least once per year |
| Never |
| Don't Know |
| Not Applicable/Not needed for my work |
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| 8 |
Question: |
In the past 12 months, how often have you used the Tier 1 Genomic Applications Toolkit for Public Health Departments? |
| Answer (Multiple Choice, One Answer) |
Daily |
| Weekly |
| Monthly |
| A few times per year |
| At least once per year |
| Never |
| Don't Know |
| Not Applicable/Not needed for my work |
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| 9 |
Question: |
In the past 12 months, how often have you used the State Genomics Implementation Map? |
| Answer (Multiple Choice, One Answer) |
Daily |
| Weekly |
| Monthly |
| A few times per year |
| At least once per year |
| Never |
| Don't Know |
| Not Applicable/Not needed for my work |
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| INTENT TO USE |
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| 10 |
Question |
I intend to access the Office of Public Health Genomics website in the future. |
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| Answer (Multiple Choice, One Answer) |
Extremely Likely |
| Likely |
| Neutral |
| Unlikely |
| Extremely Unlikely |
| Not Applicable/Not Needed for my work |
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| 11 |
Question |
I intend to use the Public Health Genomics Knowledge Base in the future. |
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| Answer (Multiple Choice, One Answer) |
Extremely Likely |
| Likely |
| Neutral |
| Unlikely |
| Extremely Unlikely |
| Not Applicable/Not Needed for my work |
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| 12 |
Question |
I intend to use the Office of Tier Table Database in the future. |
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| Answer (Multiple Choice, One Answer) |
Extremely Likely |
| Likely |
| Neutral |
| Unlikely |
| Extremely Unlikely |
| Not Applicable/Not Needed for my work |
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| 13 |
Question |
I intend to use the Tier 1 Genomic Applications Toolkit for Public Health Departments in the future. |
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| Answer (Multiple Choice, One Answer) |
Extremely Likely |
| Likely |
| Neutral |
| Unlikely |
| Extremely Unlikely |
| Not Applicable/Not Needed for my work |
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| 14 |
Question |
I intend to use the State Genomics Implementation Map in the future. |
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| Answer (Multiple Choice, One Answer) |
Extremely Likely |
| Likely |
| Neutral |
| Unlikely |
| Extremely Unlikely |
| Not Applicable/Not Needed for my work |
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| BARRIERS TO USE |
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| 15 |
Question |
What barries have limited you from using the CDC Office of Public Health Genomics resources? |
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| Answer (Multiple Choice, multiple answers and short answer) |
The website does not offer the type of information that I need |
| I was not aware of the resources |
| I am not aware of how the resources will be applicable to my current job function |
| I could not find the resources on the CDC Office of Public Health Genomics website |
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| I found the resources confusing |
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| I did not understand how to use the resources |
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| I do not have any extra time during my work schedule to utilize the CDC Office of Public Health Genomics website |
| I have not encountered any barriers |
| Don't Know |
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| 16 |
Question: |
Please provide suggesstions for improvement or additions to the Office of Public Health Genomics website. |
| Answer(Short Answer) |
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| 17 |
Question: |
Please provide suggestons for improvement or additions to the Public Health Genomics Knowledge Base. |
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| Answer(Short Answer) |
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| 18 |
Question: |
Please provide suggestons for improvement or additions to the Tier Table Database. |
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| Answer(Short Answer) |
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| 19 |
Question: |
Please provide sugestions for improvement to the Tier 1 Genomic Applications Toolkit for Public Health Departments. |
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| Answer(Short Answer) |
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| 20 |
Question: |
Please provide suggestion for improvement to the State Genomics Implementation Map. |
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| Answer(Short Answer) |
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| 21 |
Question: |
What additional online resources would be useful for the CDC Office of Public Health Genomics to provide? |
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| Answer(Short Answer) |
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| 22 |
Question |
Please provide information about activities in your state related to the following: |
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Family health history of breast or ovarian cancer |
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Family health history of colorectal or endometrial cancer |
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Family history of heart disease |
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Hereditary breast and ovarian cancer screening/testing |
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Hereditary colorectal and endometrial cancer screening/testing or Lynch syndrome screening/testing |
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Familial hypercholesterolemia screening/testing |
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Genetic counseling or testing for BRCA1 and BRCA2 mutations or other mutations associated with hereditary breast or ovarian cancer |
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Genetic counseling or testing in the mismatch repair genes (MLH1, MSH2, MSH6, and PMS2), the EPCAM gene, or other mutations associated with colorectal cancer |
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Tumor screening for Lynch syndrome using microsatellite instability testing or immunohistochemical staining for the mismatch repair proteins (MLH1, MSH2, MSH6 and PMS2) among newly diagnosed colorectal cancer patients |
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Any other genomics-related activities that you would like to share with us |
| Answer (Short Answer) |
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