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Transitioning From In-Person to Remote Clinical Research on Depression and Traumatic Brain Injury During the COVID-19 Pandemic: Study Modifications and Preliminary Feasibility From a Randomized Controlled Pilot Study.
Fisher, Lauren B; Tuchman, Sylvie; Curreri, Andrew J; Markgraf, Maggie; Nyer, Maren B; Cassano, Paolo; Iverson, Grant L; Fava, Maurizio; Zafonte, Ross D; Pedrelli, Paola.
Afiliação
  • Fisher LB; Department of Psychiatry, Massachusetts General Hospital, Boston, MA, United States.
  • Tuchman S; Department of Psychiatry, Harvard Medical School, Boston, MA, United States.
  • Curreri AJ; Department of Psychiatry, Massachusetts General Hospital, Boston, MA, United States.
  • Markgraf M; Department of Psychological & Brain Sciences, Boston University, Boston, MA, United States.
  • Nyer MB; Department of Psychiatry, Massachusetts General Hospital, Boston, MA, United States.
  • Cassano P; Department of Psychiatry, Massachusetts General Hospital, Boston, MA, United States.
  • Iverson GL; Department of Psychiatry, Harvard Medical School, Boston, MA, United States.
  • Fava M; Department of Psychiatry, Massachusetts General Hospital, Boston, MA, United States.
  • Zafonte RD; Department of Psychiatry, Harvard Medical School, Boston, MA, United States.
  • Pedrelli P; Department of Physical Medicine and Rehabilitation, Harvard Medical School, Boston, MA, United States.
JMIR Form Res ; 5(12): e28734, 2021 Dec 01.
Article em En | MEDLINE | ID: mdl-34662285
BACKGROUND: Telehealth has provided many researchers, especially those conducting psychosocial research, with the tools necessary to transition from in-person to remote clinical trials during the COVID-19 pandemic. A growing body of research supports the effectiveness of telemental health for a variety of psychiatric conditions, but few studies have examined telemental health for individuals with comorbid medical diagnoses. Furthermore, little is known about the remote implementation of clinical trials examining telemental health interventions. OBJECTIVE: This paper outlines the procedural modifications used to facilitate conversion of an in-person randomized controlled trial of cognitive behavioral therapy (CBT) for depression in individuals with traumatic brain injury (TBI; CBT-TBI) to a telemental health study administered remotely. METHODS: Given the nature of remote implementation and specific challenges experienced by individuals with TBI, considerations related to treatment delivery, remote consent, data management, neuropsychological assessment, safety monitoring, and delivery of supportive material have been discussed. Feasibility, acceptability, and safety were evaluated by examining attendance and participant responses on self-report measures of treatment satisfaction and suicidal behavior. RESULTS: High rates of treatment attendance, assessment completion, study retention, and satisfaction with the intervention and modality were reported by participants who completed at least one telemental health CBT-TBI session. CONCLUSIONS: Study modifications are necessary when conducting a study remotely, and special attention should be paid to comorbidities and population-specific challenges (eg, cognitive impairment). Preliminary data support the feasibility, acceptability, and safety of remotely conducting a randomized controlled trial of CBT-TBI. TRIAL REGISTRATION: ClinicalTrials.gov NCT03307070; https://clinicaltrials.gov/ct2/show/NCT03307070.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Tipo de estudo: Clinical_trials Idioma: En Revista: JMIR Form Res Ano de publicação: 2021 Tipo de documento: Article País de afiliação: Estados Unidos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Tipo de estudo: Clinical_trials Idioma: En Revista: JMIR Form Res Ano de publicação: 2021 Tipo de documento: Article País de afiliação: Estados Unidos