SARS-COV-2 Screening in Dialysis Facilities
Primary Purpose
End-stage Renal Disease, SARS-CoV-2 Acute Respiratory Disease, Dialysis; Complications
Status
Active
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Offering SARS-CoV-2 test
Sponsored by
About this trial
This is an interventional screening trial for End-stage Renal Disease focused on measuring Screening, Underserved communities, RADx-UP
Eligibility Criteria
Inclusion Criteria:
Facility
- An established US Renal Care in-center hemodialysis facility located in a county with at least two US Renal Care facilities
- Facility governing board (Medical Director, Facility Manager, Social Worker and Charge Nurses) willingness to participate Patient
- Treatment at US Renal Care in-center hemodialysis facility
- Age ≥ 18 years
Exclusion Criteria:
Patient
- Unwillingness to share anonymized clinical (electronic health record) or serum samples drawn during routine dialysis care (i.e., without an additional needlestick). If a patient declines offered testing he/she will still be part of the analyses as long as he/she is willing to share clinical data
- Dementia or cognitive impairment, with inability to comprehend 'opting out' of participation
Sites / Locations
- US Renal Care
Arms of the Study
Arm 1
Arm 2
Arm Type
Active Comparator
Active Comparator
Arm Label
Static frequency
Dynamic frequency
Arm Description
Test based screening for SARS-CoV-2 every two weeks
Test based screening for SARS-CoV-2 ranging from once a week to once every four weeks anchored to county COVID-19 case rates
Outcomes
Primary Outcome Measures
Test acceptance rate
Secondary Outcome Measures
Deaths
Hospitalizations
Change in facility scores on In-Center Hemodialysis Consumer Assessment of Healthcare Providers and Systems (ICH CAHPS) Survey
this survey is administered annually at each dialysis facility dialysis facility (based on Centers for Medicare Services regulation)
Full Information
NCT ID
NCT05225298
First Posted
January 24, 2022
Last Updated
September 18, 2023
Sponsor
Stanford University
Collaborators
National Institute on Minority Health and Health Disparities (NIMHD), National Institute of Allergy and Infectious Diseases (NIAID)
1. Study Identification
Unique Protocol Identification Number
NCT05225298
Brief Title
SARS-COV-2 Screening in Dialysis Facilities
Official Title
SARS-COV-2 Screening in Dialysis Facilities: Building an Optimal Strategy to Protect High Risk Populations
Study Type
Interventional
2. Study Status
Record Verification Date
September 2023
Overall Recruitment Status
Active, not recruiting
Study Start Date
February 6, 2023 (Actual)
Primary Completion Date
March 2024 (Anticipated)
Study Completion Date
March 2026 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Stanford University
Collaborators
National Institute on Minority Health and Health Disparities (NIMHD), National Institute of Allergy and Infectious Diseases (NIAID)
4. Oversight
Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Product Manufactured in and Exported from the U.S.
No
Data Monitoring Committee
Yes
5. Study Description
Brief Summary
Patients receiving dialysis are one of the highest risk groups for serious illness with SARS-CoV-2 infection. In addition to the inherent risks of travel to and dialysis within indoor facilities, patients receiving dialysis are more likely to be older, non-white, from disadvantaged backgrounds, and have impaired immune responses to viral infections and vaccinations. Universal testing offered at hemodialysis facilities could shield this vulnerable population from exposure, enable early identification and treatment for those affected, and reduce transmission to other patients and family members. In this pragmatic cluster randomized controlled trial as part of NIH RADx-UP Consortium, we will randomize 62 US Renal Care facilities with an estimated 2480 patients to static versus dynamic universal screening testing strategies. Static universal screening will involve offering patients SARS-CoV-2 screening tests every two weeks; the dynamic universal screening strategy will vary the frequency of testing from once every week to once every four weeks, depending on community COVID-19 case rates. We hypothesize that patients dialyzing at facilities randomized to a dynamic testing frequency responsive to community case rates will have higher test acceptability (primary outcome), experience lower rates of COVID-19 death and hospitalization, and report better experience-of-care metrics.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
End-stage Renal Disease, SARS-CoV-2 Acute Respiratory Disease, Dialysis; Complications
Keywords
Screening, Underserved communities, RADx-UP
7. Study Design
Primary Purpose
Screening
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
2389 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Static frequency
Arm Type
Active Comparator
Arm Description
Test based screening for SARS-CoV-2 every two weeks
Arm Title
Dynamic frequency
Arm Type
Active Comparator
Arm Description
Test based screening for SARS-CoV-2 ranging from once a week to once every four weeks anchored to county COVID-19 case rates
Intervention Type
Behavioral
Intervention Name(s)
Offering SARS-CoV-2 test
Intervention Description
A pragmatic cluster (facility-level) randomized clinical trial, comparing test-based screening performed at a static (every two weeks) frequency versus a dynamic frequency (ranging from once a week to once every four weeks) anchored to county COVID-19 case rates
Primary Outcome Measure Information:
Title
Test acceptance rate
Time Frame
3 months
Secondary Outcome Measure Information:
Title
Deaths
Time Frame
2 years
Title
Hospitalizations
Time Frame
2 years
Title
Change in facility scores on In-Center Hemodialysis Consumer Assessment of Healthcare Providers and Systems (ICH CAHPS) Survey
Description
this survey is administered annually at each dialysis facility dialysis facility (based on Centers for Medicare Services regulation)
Time Frame
18 months
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Facility
An established US Renal Care in-center hemodialysis facility located in a county with at least two US Renal Care facilities
Facility governing board (Medical Director, Facility Manager, Social Worker and Charge Nurses) willingness to participate Patient
Treatment at US Renal Care in-center hemodialysis facility
Age ≥ 18 years
Exclusion Criteria:
Patient
Unwillingness to share anonymized clinical (electronic health record) or serum samples drawn during routine dialysis care (i.e., without an additional needlestick). If a patient declines offered testing he/she will still be part of the analyses as long as he/she is willing to share clinical data
Dementia or cognitive impairment, with inability to comprehend 'opting out' of participation
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Shuchi Anand, MD
Organizational Affiliation
Stanford University
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Julie Parsonnet, MD
Organizational Affiliation
Stanford University
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Glenn Chertow, MD
Organizational Affiliation
Stanford University
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Geoff Block, MD
Organizational Affiliation
US Renal Care
Official's Role
Study Director
Facility Information:
Facility Name
US Renal Care
City
Plano
State/Province
Texas
ZIP/Postal Code
75024
Country
United States
12. IPD Sharing Statement
Plan to Share IPD
Yes
IPD Sharing Plan Description
Anonymized data will be shared with NIH Radx-UP data repository.
Learn more about this trial
SARS-COV-2 Screening in Dialysis Facilities
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