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
Department of Psychiatry, Massachusetts General Hospital, Boston, MA, United States.
Department of Psychiatry, Harvard Medical School, Boston, MA, United States.
JMIR Form Res. 2021 Dec 1;5(12):e28734. doi: 10.2196/28734.
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.
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.
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.
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.
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.
ClinicalTrials.gov NCT03307070; https://clinicaltrials.gov/ct2/show/NCT03307070.
远程医疗为许多研究人员,尤其是那些进行社会心理研究的人员,提供了在新冠疫情期间从面对面临床试验过渡到远程临床试验所需的工具。越来越多的研究支持远程心理健康服务对多种精神疾病的有效性,但很少有研究考察合并躯体疾病诊断个体的远程心理健康服务。此外,对于考察远程心理健康干预措施的临床试验的远程实施情况知之甚少。
本文概述了为促进将一项针对创伤性脑损伤(TBI)个体抑郁症的认知行为疗法(CBT)面对面随机对照试验(CBT-TBI)转换为远程实施的远程心理健康研究而进行的程序修改。
鉴于远程实施的性质以及TBI个体所经历的特定挑战,讨论了与治疗提供、远程同意、数据管理、神经心理学评估、安全监测和支持性材料提供相关的考虑因素。通过检查出勤率以及参与者对治疗满意度和自杀行为的自我报告测量的反应来评估可行性、可接受性和安全性。
完成至少一次远程心理健康CBT-TBI治疗的参与者报告了高治疗出勤率、评估完成率、研究保留率以及对干预措施和方式的满意度。
远程开展研究时需要进行研究修改,并且应特别关注合并症和特定人群的挑战(例如认知障碍)。初步数据支持远程开展CBT-TBI随机对照试验的可行性、可接受性和安全性。
ClinicalTrials.gov NCT03307070;https://clinicaltrials.gov/ct2/show/NCT033
07070。