Efficient designs for three-sequence stepped wedge trials with continuous recruitment.

IF 2.2 3区 医学 Q3 MEDICINE, RESEARCH & EXPERIMENTAL Clinical Trials Pub Date : 2024-12-01 Epub Date: 2024-05-21 DOI:10.1177/17407745241251780
Richard Hooper, Olivier Quintin, Jessica Kasza
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Abstract

Background/aims: The standard approach to designing stepped wedge trials that recruit participants in a continuous stream is to divide time into periods of equal length. But the choice of design in such cases is infinitely more flexible: each cluster could cross from the control to the intervention at any point on the continuous time-scale. We consider the case of a stepped wedge design with clusters randomised to just three sequences (designs with small numbers of sequences may be preferred for their simplicity and practicality) and investigate the choice of design that minimises the variance of the treatment effect estimator under different assumptions about the intra-cluster correlation.

Methods: We make some simplifying assumptions in order to calculate the variance: in particular that we recruit the same number of participants, m, from each cluster over the course of the trial, and that participants present at regularly spaced intervals. We consider an intra-cluster correlation that decays exponentially with separation in time between the presentation of two individuals from the same cluster, from a value of ρ for two individuals who present at the same time, to a value of ρτ for individuals presenting at the start and end of the trial recruitment interval. We restrict attention to three-sequence designs with centrosymmetry - the property that if we reverse time and swap the intervention and control conditions then the design looks the same. We obtain an expression for the variance of the treatment effect estimator adjusted for effects of time, using methods for generalised least squares estimation, and we evaluate this expression numerically for different designs, and for different parameter values.

Results: There is a two-dimensional space of possible three-sequence, centrosymmetric stepped wedge designs with continuous recruitment. The variance of the treatment effect estimator for given ρ and τ can be plotted as a contour map over this space. The shape of this variance surface depends on τ and on the parameter mρ/(1-ρ), but typically indicates a broad, flat region of close-to-optimal designs. The 'standard' design with equally spaced periods and 1:1:1 allocation rarely performs well, however.

Conclusions: In many different settings, a relatively simple design can be found (e.g. one based on simple fractions) that offers close-to-optimal efficiency in that setting. There may also be designs that are robustly efficient over a wide range of settings. Contour maps of the kind we illustrate can help guide this choice. If efficiency is offered as one of the justifications for using a stepped wedge design, then it is worth designing with optimal efficiency in mind.

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连续招募的三序列阶梯式楔形试验的高效设计。
背景/目的:设计连续招募参与者的阶梯式楔形试验的标准方法是将时间划分为等长的时段。但在这种情况下,设计方案的选择具有无限的灵活性:每个群组都可以在连续时间尺度上的任何一点从对照组转向干预组。我们考虑了阶梯式楔形设计的情况,即分组随机分配到三个序列(序列数量少的设计可能更简单实用),并研究了在分组内相关性的不同假设下,如何选择设计才能使治疗效果估计值的方差最小:为了计算方差,我们做了一些简化假设:特别是在试验过程中,我们从每个群组招募相同数量的参与者(m),并且参与者按固定间隔出现。我们考虑的群组内相关性是随着来自同一群组的两个个体出现的时间间隔呈指数衰减,从两个同时出现的个体的 ρ 值,到在试验招募间隔开始和结束时出现的个体的 ρτ 值。我们将注意力限制在具有中心对称性的三序列设计上,即如果我们颠倒时间并交换干预和对照条件,设计看起来是一样的。我们利用广义最小二乘法估算方法,得到了根据时间效应调整后的治疗效果估计方差表达式,并针对不同设计和不同参数值对该表达式进行了数值评估:结果:存在一个二维空间,其中可能包含连续招募的三序列、中心对称阶梯楔形设计。给定 ρ 和 τ 时,治疗效果估计值的方差可以绘制成该空间的等高线图。该方差曲面的形状取决于 τ 和参数 mρ/(1-ρ),但通常表示一个接近最优设计的宽阔平坦区域。然而,等间距周期和 1:1:1 分配的 "标准 "设计很少有好的表现:在许多不同的环境中,都可以找到一种相对简单的设计(如基于简单分数的设计),在该环境中提供接近最优的效率。也可能有一些设计在各种情况下都能保持稳定的效率。我们举例说明的这种等高线图可以帮助指导这种选择。如果效率是使用阶梯楔形设计的理由之一,那么在设计时就应该考虑到最佳效率。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Clinical Trials
Clinical Trials 医学-医学:研究与实验
CiteScore
4.10
自引率
3.70%
发文量
82
审稿时长
6-12 weeks
期刊介绍: Clinical Trials is dedicated to advancing knowledge on the design and conduct of clinical trials related research methodologies. Covering the design, conduct, analysis, synthesis and evaluation of key methodologies, the journal remains on the cusp of the latest topics, including ethics, regulation and policy impact.
期刊最新文献
Challenges in conducting efficacy trials for new COVID-19 vaccines in developed countries. Society for Clinical Trials Data Monitoring Committee initiative website: Closing the gap. A comparison of computational algorithms for the Bayesian analysis of clinical trials. Comparison of Bayesian and frequentist monitoring boundaries motivated by the Multiplatform Randomized Clinical Trial. Efficient designs for three-sequence stepped wedge trials with continuous recruitment.
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