Department of Psychology, University of California, Berkeley, CA, Berkeley, USA.
RAND Corporation, Santa Monica, CA, USA.
Trials. 2023 Mar 17;24(1):198. doi: 10.1186/s13063-023-07148-9.
Serious mental illness (SMI) can have devastating consequences. Unfortunately, many patients with SMI do not receive evidence-based psychological treatment (EBPTs) in routine practice settings. One barrier is poor "fit" between EBPTs and contexts in which they are implemented. The present study will evaluate implementation and effectiveness outcomes of the Transdiagnostic Intervention for Sleep and Circadian Dysfunction (TranS-C) implemented in community mental health centers (CMHCs). TranS-C was designed to target a range of SMI diagnoses by addressing a probable mechanism and predictor of SMI: sleep and circadian problems. We will investigate whether adapting TranS-C to fit CMHC contexts improves providers' perceptions of fit and patient outcomes.
TranS-C will be implemented in at least ten counties in California, USA (N = 96 providers; N = 576 clients), via facilitation. CMHC sites are cluster-randomized by county to Adapted TranS-C or Standard TranS-C. Within each county, patients are randomized to immediate TranS-C or usual care followed by delayed treatment with TranS-C (UC-DT). Aim 1 will compare TranS-C (combined Adapted and Standard) with UC-DT on improvements in sleep and circadian problems, functional impairment, and psychiatric symptoms. Sleep and circadian problems will also be tested as a mediator between treatment condition (combined TranS-C versus UC-DT) and functional impairment/psychiatric symptoms. Aim 2 will evaluate whether Adapted TranS-C is superior to Standard TranS-C with respect to provider perceptions of fit. Aim 3 will evaluate whether the relation between TranS-C treatment condition (Adapted versus Standard) and patient outcomes is mediated by better provider perceptions of fit in the Adapted condition. Exploratory analyses will (1) compare Adapted versus Standard TranS-C on patient perceptions of credibility/improvement and select PhenX Toolkit outcomes and (2) evaluate possible moderators.
This trial has the potential to (a) expand support for TranS-C, a promising transdiagnostic treatment delivered to patients with SMI in CMHCs; (b) take steps toward addressing challenges faced by providers in delivering EBPTs (i.e., high caseloads, complex patients, poor fit); and (c) advance evidence on causal strategies (i.e., adapting treatments to fit context) in implementation science.
Clinicaltrials.gov NCT04154631. Registered on 6 November 2019. https://clinicaltrials.gov/ct2/show/NCT04154631.
严重的精神疾病(SMI)可能会产生毁灭性的后果。不幸的是,许多患有 SMI 的患者在常规实践环境中并未接受基于证据的心理治疗(EBPT)。其中一个障碍是 EBPT 与实施它们的环境之间的“适配性”差。本研究将评估在社区心理健康中心(CMHC)中实施的跨诊断睡眠和昼夜节律障碍干预(TranS-C)的实施和效果结果。TranS-C 通过解决精神疾病的一个可能机制和预测因素:睡眠和昼夜节律问题,旨在针对一系列 SMI 诊断。我们将研究是否通过调整 TranS-C 以适应 CMHC 环境来改善提供者对适应度的感知和患者的结果。
TranS-C 将通过促进至少在加利福尼亚州的十个县(N=96 名提供者;N=576 名患者)实施。CMHC 站点按县进行集群随机分配,接受适应性 TranS-C 或标准 TranS-C。在每个县内,患者随机接受即时 TranS-C 或常规治疗,然后延迟接受 TranS-C(UC-DT)治疗。目的 1 将比较 TranS-C(综合适应性和标准性)与 UC-DT 在睡眠和昼夜节律问题、功能障碍和精神症状方面的改善。睡眠和昼夜节律问题也将作为治疗条件(综合 TranS-C 与 UC-DT)与功能障碍/精神症状之间的中介进行测试。目的 2 将评估适应性 TranS-C 在提供者对适应性的感知方面是否优于标准 TranS-C。目的 3 将评估 TranS-C 治疗条件(适应性与标准)与患者结果之间的关系是否通过适应性条件下提供者对适应性的更好感知来介导。探索性分析将(1)比较适应性与标准 TranS-C 对患者对可信度/改善的看法和选择 PhenX 工具包结果;(2)评估可能的调节因素。
这项试验有可能(a)扩大对 TranS-C 的支持,这是一种针对 CMHC 中患有 SMI 的患者的有前途的跨诊断治疗方法;(b)采取措施应对提供者在提供 EBPT 时面临的挑战(即,高工作量、复杂患者、适配性差);(c)推进实施科学中因果策略(即,调整治疗以适应环境)的证据。
Clinicaltrials.gov NCT04154631。于 2019 年 11 月 6 日注册。https://clinicaltrials.gov/ct2/show/NCT04154631。