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 @ 11:53 PM
Ignite Modification Date:
2025-12-24 @ 11:53 PM
NCT ID:
NCT04086251
Eligibility Criteria:
Inclusion Criteria:
1. Adult oncology patients over the age of 18 who are receiving chemotherapy.
2. Adult oncology in-patients over the age of 18 who are being being discharged.
3. Patients who have the mental capacity to understand how to use the devices and phone App; or patients who have a 24-hour caregiver who can manage the devices and complete patient surveys.
4. Patients who speak, read, and understand English.
5. Patients who have access to a smart phone.
Exclusion Criteria:
1. Non-English speaking patients.
2. Pregnant women.
3. Tattoos on outer side of upper arm (where the heart rate device will be worn).
4. Infant or pediatric (age less than 18).
5. Dementia, unless accompanied by a full-time caregiver.
6. Physically unable to wear the associated wearable devices; for example, amputees (preventing the placement of wearable devices worn on the arm).
7. Existence of open wounds or skin breakdown in the designated area for wearable device placement or on patients with conditions of irritable skin, per clinician judgment based on patient assessment.
8. Body mass index (BMI) \>35 kg/m2, with conical shaped upper arms with significant adipose tissue (BP measurements might not perform properly).
9. Hospice patients who have an 'advanced directive'.
Healthy Volunteers:
False
Sex:
ALL
Minimum Age:
18 Years
Study:
NCT04086251
Study Brief:
Protocol Section:
NCT04086251