Best practices to reduce COVID-19 in group homes for individuals with serious mental illness and intellectual and developmental disabilities: Protocol for a hybrid type 1 effectiveness-implementation cluster randomized trial.


Journal

Contemporary clinical trials
ISSN: 1559-2030
Titre abrégé: Contemp Clin Trials
Pays: United States
ID NLM: 101242342

Informations de publication

Date de publication:
02 2023
Historique:
received: 25 08 2022
revised: 29 11 2022
accepted: 13 12 2022
pubmed: 21 12 2022
medline: 15 2 2023
entrez: 20 12 2022
Statut: ppublish

Résumé

People with serious mental illness (SMI) and intellectual disabilities and/or developmental disabilities (ID/DD) living in group homes (GHs) and residential staff are at higher risk for COVID-19 infection, hospitalization, and death compared with the general population. We describe a hybrid type 1 effectiveness-implementation cluster randomized trial to assess evidence-based infection prevention practices to prevent COVID-19 for residents with SMI or ID/DD and the staff in GHs. The trial will use a cluster randomized design in 400 state-funded GHs in Massachusetts for adults with SMI or ID/DD to compare effectiveness and implementation of "Tailored Best Practices" (TBP) consisting of evidence-based COVID-19 infection prevention practices adapted for residents with SMI and ID/DD and GH staff; to "General Best Practices" (GBP), consisting of required standard of care reflecting state and federal standard general guidelines for COVID-19 prevention in GHs. External (i.e., community-based research staff) and internal (i.e., GH staff leadership) personnel will facilitate implementation of TBP. The primary effectiveness outcome is incident SARS-CoV-2 infection and secondary effectiveness outcomes include COVID-19-related hospitalizations and mortality in GHs. The primary implementation outcomes are fidelity to TBP and rates of COVID-19 vaccination. Secondary implementation outcomes are adoption, adaptation, reach, and maintenance. Outcomes will be assessed at baseline, 3-, 6-, 9-, 12-, and 15-months post-randomization. This study will advance knowledge on comparative effectiveness and implementation of two different strategies to prevent COVID-19-related infection, morbidity, and mortality and promote fidelity and adoption of these interventions in high-risk GHs for residents with SMI or ID/DD and staff. NCT04726371.

Sections du résumé

BACKGROUND
People with serious mental illness (SMI) and intellectual disabilities and/or developmental disabilities (ID/DD) living in group homes (GHs) and residential staff are at higher risk for COVID-19 infection, hospitalization, and death compared with the general population.
METHODS
We describe a hybrid type 1 effectiveness-implementation cluster randomized trial to assess evidence-based infection prevention practices to prevent COVID-19 for residents with SMI or ID/DD and the staff in GHs. The trial will use a cluster randomized design in 400 state-funded GHs in Massachusetts for adults with SMI or ID/DD to compare effectiveness and implementation of "Tailored Best Practices" (TBP) consisting of evidence-based COVID-19 infection prevention practices adapted for residents with SMI and ID/DD and GH staff; to "General Best Practices" (GBP), consisting of required standard of care reflecting state and federal standard general guidelines for COVID-19 prevention in GHs. External (i.e., community-based research staff) and internal (i.e., GH staff leadership) personnel will facilitate implementation of TBP. The primary effectiveness outcome is incident SARS-CoV-2 infection and secondary effectiveness outcomes include COVID-19-related hospitalizations and mortality in GHs. The primary implementation outcomes are fidelity to TBP and rates of COVID-19 vaccination. Secondary implementation outcomes are adoption, adaptation, reach, and maintenance. Outcomes will be assessed at baseline, 3-, 6-, 9-, 12-, and 15-months post-randomization.
CONCLUSIONS
This study will advance knowledge on comparative effectiveness and implementation of two different strategies to prevent COVID-19-related infection, morbidity, and mortality and promote fidelity and adoption of these interventions in high-risk GHs for residents with SMI or ID/DD and staff.
CLINICAL TRIAL REGISTRATION NUMBER
NCT04726371.

Identifiants

pubmed: 36539061
pii: S1551-7144(22)00379-2
doi: 10.1016/j.cct.2022.107053
pmc: PMC9758744
pii:
doi:

Substances chimiques

COVID-19 Vaccines 0

Banques de données

ClinicalTrials.gov
['NCT04726371']

Types de publication

Clinical Trial Protocol Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

107053

Informations de copyright

Copyright © 2022 Elsevier Inc. All rights reserved.

Déclaration de conflit d'intérêts

Declaration of Competing Interest The authors declare the following financial interests/personal relationships which may be considered as potential competing interests: Dr. Skotko occasionally consults on the topic of Down syndrome through Gerson Lehrman Group. He receives remuneration from Down syndrome non-profit organizations for speaking engagements and associated travel expenses. Dr. Skotko receives annual royalties from Woodbine House, Inc., for the publication of his book, Fasten Your Seatbelt: A Crash Course on Down Syndrome for Brothers and Sisters. Within the past two years, he has received research funding from F. Hoffmann-La Roche, Inc., AC Immune, and LuMind Research Down Syndrome Foundation to conduct clinical trials for people with Down syndrome. Dr. Skotko is occasionally asked to serve as an expert witness for legal cases where Down syndrome is discussed. Dr. Skotko serves in a non-paid capacity on the Honorary Board of Directors for the Massachusetts Down Syndrome Congress and the Professional Advisory Committee for the National Center for Prenatal and Postnatal Down Syndrome Resources. Dr. Skotko has a sister with Down syndrome.

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Auteurs

Julie H Levison (JH)

Harvard Medical School, Massachusetts General Hospital, Mongan Institute, 100 Cambridge St, Suite 1600, Boston, MA 02114, USA; Harvard Medical School, Massachusetts General Hospital, Department of Medicine, 55 Fruit St, Gray 7-730, Boston, MA 02114, USA. Electronic address: jlevison@partners.org.

David Krane (D)

Harvard Medical School, Massachusetts General Hospital, Mongan Institute, 100 Cambridge St, Suite 1600, Boston, MA 02114, USA.

Karen Donelan (K)

Harvard Medical School, Massachusetts General Hospital, Mongan Institute, 100 Cambridge St, Suite 1600, Boston, MA 02114, USA.

Kelly Aschbrenner (K)

Geisel School of Medicine at Dartmouth, Dartmouth-Hitchcock Medical Center, Department of Psychiatry, One Medical Center Drive, Lebanon, NH 03756, USA.

Hao D Trieu (HD)

Harvard Medical School, Massachusetts General Hospital, Mongan Institute, 100 Cambridge St, Suite 1600, Boston, MA 02114, USA.

Cindy Chau (C)

Harvard Medical School, Massachusetts General Hospital, Mongan Institute, 100 Cambridge St, Suite 1600, Boston, MA 02114, USA.

Anna Wilson (A)

Harvard Medical School, Massachusetts General Hospital, Mongan Institute, 100 Cambridge St, Suite 1600, Boston, MA 02114, USA.

Nicolas M Oreskovic (NM)

Harvard Medical School, Massachusetts General Hospital, Department of Medicine, 55 Fruit St, Gray 7-730, Boston, MA 02114, USA; Harvard Medical School, Massachusetts General Hospital, Department of Pediatrics, Division of Medical Genetics and Metabolism, Down Syndrome Program, 125 Nashua Street, Suite 821, Boston, MA 02114, USA.

Kelly Irwin (K)

Harvard Medical School, Massachusetts General Hospital, Department of Psychiatry, 55 Fruit Street, Boston, MA 02114, USA.

Lisa I Iezzoni (LI)

Harvard Medical School, Massachusetts General Hospital, Mongan Institute, 100 Cambridge St, Suite 1600, Boston, MA 02114, USA.

Haiyi Xie (H)

Geisel School of Medicine at Dartmouth, Department of Biomedical Data Science, Williamson Translational Research Building, Third Floor, HB 7261, 1 Medical Center Drive, Lebanon, NH 03756, USA.

Ronita Samuels (R)

Harvard Medical School, Massachusetts General Hospital, Mongan Institute, 100 Cambridge St, Suite 1600, Boston, MA 02114, USA.

Paula Silverman (P)

Vinfen Corporation, 950 Cambridge Street, Cambridge, MA 02141, USA.

Joey Batson (J)

Vinfen Corporation, 950 Cambridge Street, Cambridge, MA 02141, USA.

Ahmed Fathi (A)

Vinfen Corporation, 950 Cambridge Street, Cambridge, MA 02141, USA.

Stefanie Gamse (S)

Vinfen Corporation, 950 Cambridge Street, Cambridge, MA 02141, USA.

Sibyl Holland (S)

Vinfen Corporation, 950 Cambridge Street, Cambridge, MA 02141, USA.

Jessica Wolfe (J)

Vinfen Corporation, 950 Cambridge Street, Cambridge, MA 02141, USA.

Kim Shellenberger (K)

Vinfen Corporation, 950 Cambridge Street, Cambridge, MA 02141, USA.

Elizabeth Cella (E)

Vinfen Corporation, 950 Cambridge Street, Cambridge, MA 02141, USA.

Bruce Bird (B)

Vinfen Corporation, 950 Cambridge Street, Cambridge, MA 02141, USA.

Brian G Skotko (BG)

Harvard Medical School, Massachusetts General Hospital, Department of Pediatrics, Division of Medical Genetics and Metabolism, Down Syndrome Program, 125 Nashua Street, Suite 821, Boston, MA 02114, USA; Harvard Medical School, Massachusetts General Hospital, Department of Pediatrics, 55 Fruit Street, Boston, MA 02214, USA.

Stephen Bartels (S)

Harvard Medical School, Massachusetts General Hospital, Mongan Institute, 100 Cambridge St, Suite 1600, Boston, MA 02114, USA; Harvard Medical School, Massachusetts General Hospital, Department of Medicine, 55 Fruit St, Gray 7-730, Boston, MA 02114, USA.

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