Eligibility Module
The Eligibility Module contains detailed information about who can participate in the clinical trial. This includes eligibility criteria, age restrictions, gender requirements, healthy volunteer status, and study population descriptions, helping researchers understand who is eligible to participate in the study.
Eligibility Module path is as follows:
Study -> Protocol Section -> Eligibility Module
Eligibility Module
Ignite Creation Date:
2025-12-24 @ 11:57 PM
Ignite Modification Date:
2025-12-24 @ 11:57 PM
NCT ID:
NCT02682251
Eligibility Criteria:
FOCUS GROUPS
Inclusion Criteria:
1. Remotely monitored with CRT-CIED
* focus groups 1 \& 2: implant ≤ 12 months
* focus groups 3 \& 4: implant ≥ 12 months
2. Current patient of PPG-Cardiology
3. History of HFrEF (heart failure in the setting of reduced ejection fraction)
4. Access to computer and internet
5. \*Ability to provide informed consent
6. \*Age ≥ 18 years
* 5 and 6 must apply to caregivers, partners, and/or support persons
Exclusion Criteria:
1. Not remotely monitored with CRT-CIED
2. Not current patient of PPG-Cardiology
3. No history of HFrEF
4. Pacemaker dependent
5. Does not have access to computer and internet
6. \*Inability to provide informed consent
7. \*Age \< 18 years
8. \*Does not meet inclusion criteria
* Only 6, 7, and 8 apply to caregivers, partners, and/or support persons
TECHNOLOGY TRIAL
Inclusion Criteria:
1. Remotely monitored with Biotronik CRT-CIED for more than 60 days
2. Ability to provide informed consent
3. Age ≥ 18 years
4. Willing to have MyChart or proxy to MyChart
5. Current patient of PPG-Cardiology
6. History of HFrEF
Exclusion Criteria:
1. Do not have a Biotronik CRT
2. Have a Biotronik CRT-CIED for less than 60 days
3. Not being remotely monitored with a Biotronik CRT-CIED
4. No history of HFrEF
5. Inability to provide informed consent
6. Age \< 18 years
7. Lack of internet access or otherwise unable to access MyChart
8. Pacemaker dependency
9. Does not meet inclusion criteria
Healthy Volunteers:
False
Sex:
ALL
Minimum Age:
18 Years
Study:
NCT02682251
Study Brief:
Protocol Section:
NCT02682251