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Using virtual multiteam systems to conduct a multisite randomized clinical trial in the part C early intervention system: Benefits, challenges, and lessons learned.
Ingersoll, Brooke; Espinel, Anthuanet; Nauman, Julia; Broder-Fingert, Sarabeth; Carter, Alice S; Sheldrick, R Christopher; Stone, Wendy L; Wainer, Allison L.
Afiliação
  • Ingersoll B; Department of Psychology, Michigan State University, 316 Physics Rd., Room 105B, East Lansing, MI 48824, USA. Electronic address: ingers19@msu.edu.
  • Espinel A; Department of Psychology, Michigan State University, 316 Physics Rd., Room 105B, East Lansing, MI 48824, USA.
  • Nauman J; Department of Psychology, Michigan State University, 316 Physics Rd., Room 105B, East Lansing, MI 48824, USA.
  • Broder-Fingert S; University of Massachusetts Chan Medical School, Worcester, MA, USA.
  • Carter AS; Department of Psychology, University of Massachusetts Boston, 100 Morrissey Boulevard, Boston, MA 02125, USA.
  • Sheldrick RC; University of Massachusetts Chan Medical School, Worcester, MA, USA.
  • Stone WL; Department of Psychology, University of Washington, Guthrie Hall Box 351525, Seattle, WA 98195, USA.
  • Wainer AL; Autism Assessment, Research, and Treatment Center, Department of Psychiatry and Behavioral Sciences, Rush University Medical Center, 1645 W. Jackson Blvd., Suite 603, Chicago, IL 60612, USA.
Contemp Clin Trials ; 143: 107585, 2024 Aug.
Article em En | MEDLINE | ID: mdl-38821261
ABSTRACT
BACKGROUND/

AIMS:

COVID-19 necessitated a shift to virtual data collection for many research projects, providing the opportunity for novel approaches to carrying out multi-site clinical trials. Virtual multiteam systems (VMTS) are a type of team structure in which multiple geographically dispersed teams collaborate using technology-mediated communication. The article presents a case study of our use of VMTS, in response to COVID-19, to carry out a multisite randomized hybrid effectiveness-implementation trial of a caregiver-implemented intervention.

METHODS:

We describe how we modified our team structure from predominantly site-specific, co-located teams to predominantly cross-site, virtual teams. We then present examples of how we have conducted the two primary data collection activities virtually. To demonstrate the feasibility of this approach, we present participant demographic information, the percent of cross-site data collection activities, and fidelity data.

RESULTS:

In the first 20 months of data collection, we have enrolled 108 EI providers and 132 families, with 17% and 9% attrition respectively. The family sample is highly diverse in terms of race/ethnicity, parent education, and household income. The majority of provider training activities and roughly 50% of family assessment activities have been conducted cross-site. Fidelity is high, with no differences across site.

CONCLUSIONS:

Our data illustrate the feasibility of using virtual teams, training, and assessment in a multisite clinical trial in the Part C system. We discuss the strengths and challenges of this approach, as well as lessons learned to facilitate the planning of future multisite randomized clinical trials which may benefit from this approach. CLINICAL TRIALS NCT05114538.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: COVID-19 Limite: Female / Humans / Male Idioma: En Revista: Contemp Clin Trials Assunto da revista: MEDICINA / TERAPEUTICA Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: COVID-19 Limite: Female / Humans / Male Idioma: En Revista: Contemp Clin Trials Assunto da revista: MEDICINA / TERAPEUTICA Ano de publicação: 2024 Tipo de documento: Article