Cardiff University | Prifysgol Caerdydd ORCA
Online Research @ Cardiff 
WelshClear Cookie - decide language by browser settings

Clinical trial simulation: planning with the OCTAVE framework, implementation and validation principles

Lee, Kim May, Choodari-Oskooei, Babak, Grayling, Michael J, Jacko, Peter, Kimani, Peter K, Mukherjee, Aritra, Pallmann, Philip ORCID: https://orcid.org/0000-0001-8274-9696, Parke, Tom, Robertson, David S, Wang, Ziyan, Yap, Christina and Jaki, Thomas 2026. Clinical trial simulation: planning with the OCTAVE framework, implementation and validation principles. Statistics in Medicine 45 (6-7) , e70449. 10.1002/sim.70449

[thumbnail of Statistics in Medicine - 2026 - Lee - Clinical Trial Simulation  Planning With the OCTAVE Framework  Implementation and.pdf]
Preview
PDF - Published Version
Available under License Creative Commons Attribution.

Download (726kB) | Preview

Abstract

The adoption of complex innovative clinical trial designs has steadily increased in recent years. These are trial designs that have one or more unconventional features—often resulting in multiple stages—with the goal of improving on conventional single-stage, fixed-setting designs in terms of efficiency, for example, by reducing the required sample size or the time to establish findings about an intervention. The motivation for these designs may not be difficult to follow, but their set-up and implementation is usually more challenging. Statistical properties of these designs can also be difficult to compute. Clinical trial simulation (CTS), which uses software to generate artificial data for learning, can be conducted to identify the (optimal) setting of a clinical trial, evaluate the design's statistical properties under some hypothetical scenarios for sensitivity analysis, and compare different design set-ups and data analysis strategies, all of which contribute to a better understanding of the value of unconventional features before implementing the design in an actual clinical trial. Existing literature on simulation primarily focuses on the evaluation of statistical analysis methods, with less attention on the detailed specification and planning of CTS. This tutorial presents a new framework, called OCTAVE, for outlining the details of CTS, provides practical recommendations for their implementation, and addresses key computational considerations. The target audience is trial statisticians who are involved in designing and analyzing clinical trials. This tutorial covers a range of complex innovative designs, without the expectation that readers are familiar with the mentioned examples.

Item Type: Article
Date Type: Publication
Status: Published
Schools: Schools > Medicine
Research Institutes & Centres > Centre for Trials Research (CNTRR)
Publisher: Wiley
ISSN: 0277-6715
Date of First Compliant Deposit: 16 March 2026
Date of Acceptance: 4 February 2026
Last Modified: 17 Mar 2026 10:00
URI: https://orca.cardiff.ac.uk/id/eprint/185744

Actions (repository staff only)

Edit Item Edit Item

Downloads

Downloads per month over past year

View more statistics