Clinical Trials Logo

Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT05270980
Other study ID # 20-01281
Secondary ID 3U54AG063546-02S
Status Completed
Phase N/A
First received
Last updated
Start date August 11, 2021
Est. completion date February 4, 2022

Study information

Verified date March 2023
Source NYU Langone Health
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The COVID-19 pandemic ravaged United States skilled-nursing facilities (SNFs). Novel strategies that maximize the safety and quality of life for SNF residents with ADRD and staff who care for them are urgently needed. Thus, the study's objectives are: 1. To rapidly plan and pilot test an intervention that leverages COVID-19 antibody and PCR status to pair SNF staff with residents in the safest way possible 2. To reduce reduced COVID-19 incidence rate compared to SNFs not using this novel staff-resident assignment strategy.


Recruitment information / eligibility

Status Completed
Enrollment 87
Est. completion date February 4, 2022
Est. primary completion date February 4, 2022
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria for Staff Stakeholders: - Must be employees of ArchCare - Must be members of included unit staff or those that float on those designated units - Willing to participate in focus groups or semi-structured interviews with study team Inclusion Criteria for Family Participants: - Family members of residents who reside at either TCC or MMW (ArchCare facilities) - Family member of resident who is on designated study unit or eligible to be transferred to such unit - Willing to participate in focus groups or semi-structured interviews with study team Inclusion Criteria for Resident Participants: - Resident has ability to communicate and follow simple commands - Resident has ability to communicate and follow simple commands - English- or Spanish-speaking - Resident has capacity to consent assessed with standard questions used to assess capacity or having a surrogate who can provide consent. - Must agree to have serologic testing for COVID-19 - Agrees to remain on one of the facility units of study or to be transferred to such unit Exclusion Criteria for Staff Stakeholders: - Not employees of ArchCare - Not members of included unit staff or those that float on those designated units - Not willing to participate in focus groups or semi-structured interviews with study team Exclusion Criteria for Family Participants: - Not family members of residents who reside at either TCC or MMW (ArchCare facilities) - Not family member of resident who is on designated study unit or eligible to be transferred to such unit - Not willing to participate in focus groups or semi-structured interviews with study team Exclusion Criteria for Resident Participants: - Resident is not living in the unit of intervention - Resident does not have ability to communicate and follow simple commands - Not English- or Spanish-speaking - Resident lacks capacity to consent assessed with standard questions used to assess capacity and does not have a surrogate who can provide consent. - If resident lacks capacity, that resident does not assent with surrogate who provides assent - Does not agree to have serologic testing for COVID-19 - Refuses to agree to remain on one of the facility units of study or to be transferred to such unit

Study Design


Related Conditions & MeSH terms


Intervention

Other:
Cohorting
The cohorting strategy will result in "pairing" serology-positive staff with serology-negative residents and serology-negative staff and serology-positive residents to the degree that penetration of serologic presumed immunity allows this pairing to be positive. Any resident who refuses serology testing will be treated as if they are serology negative as the safest strategy for risk of unwanted exposure.

Locations

Country Name City State
United States ArchCare at Mary Manning Walsh Home (MMW) New York New York
United States ArchCare at Terence Cardinal Cooke Health Care Center (TCC) New York New York

Sponsors (3)

Lead Sponsor Collaborator
NYU Langone Health Brown University, National Institute on Aging (NIA)

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Number of New COVID-19 Detected Infections Among Residents Up to Month 5
Secondary Number of New COVID-19 Detected Infections Among Staff Up to Month 5
Secondary Number of Hospitalizations Over Time Up to Month 5
See also
  Status Clinical Trial Phase
Withdrawn NCT06065033 - Exercise Interventions in Post-acute Sequelae of Covid-19 N/A
Completed NCT06267534 - Mindfulness-based Mobile Applications Program N/A
Completed NCT05047601 - A Study of a Potential Oral Treatment to Prevent COVID-19 in Adults Who Are Exposed to Household Member(s) With a Confirmed Symptomatic COVID-19 Infection Phase 2/Phase 3
Recruiting NCT05323760 - Functional Capacity in Patients Post Mild COVID-19 N/A
Recruiting NCT04481633 - Efficacy of Pre-exposure Treatment With Hydroxy-Chloroquine on the Risk and Severity of COVID-19 Infection N/A
Completed NCT04612972 - Efficacy, Safety and Immunogenicity of Inactivated SARS-CoV-2 Vaccines (Vero Cell) to Prevent COVID-19 in Healthy Adult Population In Peru Healthy Adult Population In Peru Phase 3
Completed NCT04537949 - A Trial Investigating the Safety and Effects of One BNT162 Vaccine Against COVID-19 in Healthy Adults Phase 1/Phase 2
Recruiting NCT05494424 - Cognitive Rehabilitation in Post-COVID-19 Condition N/A
Active, not recruiting NCT06039449 - A Study to Investigate the Prevention of COVID-19 withVYD222 in Adults With Immune Compromise and in Participants Aged 12 Years or Older Who Are at Risk of Exposure to SARS-CoV-2 Phase 3
Enrolling by invitation NCT05589376 - You and Me Healthy
Completed NCT05158816 - Extracorporal Membrane Oxygenation for Critically Ill Patients With COVID-19
Recruiting NCT04341506 - Non-contact ECG Sensor System for COVID19
Completed NCT04384445 - Zofin (Organicell Flow) for Patients With COVID-19 Phase 1/Phase 2
Completed NCT04512079 - FREEDOM COVID-19 Anticoagulation Strategy Phase 4
Completed NCT05975060 - A Study to Evaluate the Safety and Immunogenicity of an (Omicron Subvariant) COVID-19 Vaccine Booster Dose in Previously Vaccinated Participants and Unvaccinated Participants. Phase 2/Phase 3
Active, not recruiting NCT05542862 - Booster Study of SpikoGen COVID-19 Vaccine Phase 3
Terminated NCT05487040 - A Study to Measure the Amount of Study Medicine in Blood in Adult Participants With COVID-19 and Severe Kidney Disease Phase 1
Withdrawn NCT05621967 - Phonation Therapy to Improve Symptoms and Lung Physiology in Patients Referred for Pulmonary Rehabilitation N/A
Terminated NCT04498273 - COVID-19 Positive Outpatient Thrombosis Prevention in Adults Aged 40-80 Phase 3
Active, not recruiting NCT06033560 - The Effect of Non-invasive Respiratory Support on Outcome and Its Risks in Severe Acute Respiratory Syndrome Coronavirus 2 (SARS-COV-2)-Related Hypoxemic Respiratory Failure