Multiple Myeloma Clinical Trial
ImmunoCARE: Rapid, Accurate COVID Testing to Reduce Hospitalization of Immunocompromised Individuals
Summary
The investigators will examine whether a combination of at-home nucleic acid amplification tests, on-demand telemedicine, and delivery of prescriptions such as Paxlovid quickly after testing positive for COVID-19, can reduce severe outcomes and hospitalization of immunocompromised patients and those who are 65 years and older. They will also analyze whether these efforts lower the cost of care compared to standard of care.
Full Description
This study is a randomized control trial with 10,000 participants. Participation will last for a minimum of 3 months and maximum of 8 months, depending upon COVID-19 case rates. Half of participants will be randomized to the control group and continue their existing testing and healthcare practices. The remaining participants will be randomized into the intervention arm. Participants in the intervention will receive one Cue Cartridge Reader for the duration of the study and up to 10 Cue COVID Molecular tests per month for their own use and to share with others in their household. In the case that a Cue Flu+COVID Molecular Test is available through FDA EUA or other authorization, participants may be provided this multiplex test in lieu of the Cue COVID Molecular Test. All intervention participants will be asked to test themselves if they are exposed or when symptoms arise and share tests with members of their household who are exposed to COVID or symptoms arise. The primary outcome will be the number of hospitalizations. This study will also compare infection rates, ICU admissions, deaths, and cost of care between the control and intervention group. The hypothesis is that access to high sensitivity portable molecular testing and subsequent telemedicine and prescription delivery can significantly decrease hospitalization and thereby the cost of care.
Interested individuals will access the study via the MyDataHelps platform by web or app to complete the eligibility and informed consent process. Within the MyDataHelps experience, participants will complete study activities such as surveys and sharing of claims data. Participants who are randomized to the intervention group will have the option to use Cue Care should they test positive for COVID-19. Cue Care contracts licensed Healthcare providers to deliver telemedicine and treatment for COVID-19. In the case that the COVID Flu+COVID test is available, the intervention group will also have the option to use Cue Care should they test positive for Influenza.
To learn more and take the eligibility survey, visit https://ImmunoCARE.scripps.edu/
Eligibility Criteria
Inclusion Criteria:
Living in the United States
18 years or older
Can read and understand English
Use of smartphone with bluetooth, a camera and a compatible operating system (Android OS 9.0 or higher, Apple iOS 13.0 or higher)
Vaccinated against COVID-19 (completed at least the initial course, e.g. at least 2 doses of -Moderna or Pfizer, one dose of J&J)
Willing and able to participate in study interventions including:
Use of smartphone, including camera and bluetooth
Upload verification of diagnosis, if needed
Completing Surveys
Use of Cue Health App
Use of MyDataHelps Web or App
Immunocompromised due to disease or therapy, including:
Symptomatic HIV
Graft versus host disease
Immunoglobulin deficiency/Immunodeficiency
Immunosuppressive therapy
Leukemia
Lymphoma (Hodgkin or non-Hodgkin)
Metastatic Cancer
Multiple Myeloma
Solid organ malignancy
Transplant, hematopoietic stem cell
Transplant, solid organ
Age
1. 65 years and older
Able to share claims data as a member of one of the following insurance providers:
Anthem BlueCross and BlueShield
Anthem BlueCross
Empire BlueCross BlueShield
Empire BlueCross
Wellpoint
Carelon
Unicare
Simply Healthcare Plans
National Government Services, Inc.
MMM
Health Sun
HealthLink
Amerigroup
Medicare
Medicaid
Or another partner that can provide claims data on participant's behalf
Exclusion Criteria:
Unable to meet inclusion criteria
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