Remote Cardiac Monitoring Survey

This survey will be used to identify present knowledge level and experience with remote cardiac monitoring to inform content of the DIA-CSRC think tank entitled, “CSRC/DIA Think Tank: Evaluation of Mobile Technologies in CV Medicine.” 

Are presently working for a/an:

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* 1. Are presently working for a/an:

What is your primary role? (Check all that apply)

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* 2. What is your primary role? (Check all that apply)

Which of the following modalities have you or your organization implemented in a clinical trial in a remote/ambulatory setting?

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* 3. Which of the following modalities have you or your organization implemented in a clinical trial in a remote/ambulatory setting?

Please indicate your level of familiarity with the indications, capabilities and limitations of the following cardiac monitoring device types: (Scale 1-4 --with 1 = no familiarity and 4= significant familiarity)

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* 4. Please indicate your level of familiarity with the indications, capabilities and limitations of the following cardiac monitoring device types: (Scale 1-4 --with 1 = no familiarity and 4= significant familiarity)

  1 2 3 4
Standard Holter Monitor
Extended Holter Monitor
Standard Event Recorder
Autotrigger Event Recorder
Wireless Event Recorder
Mobile Cardiac Telemetry
Implantable Loop Recorder
Phone App Monitor
Who chooses the type of device that will be used for a study in your organization?

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* 5. Who chooses the type of device that will be used for a study in your organization?

Who evaluates the cardiac monitoring data generated by a study done by your organization?

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* 6. Who evaluates the cardiac monitoring data generated by a study done by your organization?

Has your organization implemented outpatient continuous ECG monitoring or other remote monitoring in a clinical trial?

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* 7. Has your organization implemented outpatient continuous ECG monitoring or other remote monitoring in a clinical trial?

If you responded yes to question seven, what clinical phase and indication was it included for?

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* 8. If you responded yes to question seven, what clinical phase and indication was it included for?

Do you see your organization implementing outpatient extended continuous monitoring in a clinical trial in the next 1-2 years?

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* 9. Do you see your organization implementing outpatient extended continuous monitoring in a clinical trial in the next 1-2 years?

Outpatient continuous ECG monitoring is most likely to be implemented in a clinical trial for:

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* 10. Outpatient continuous ECG monitoring is most likely to be implemented in a clinical trial for:

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