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Review
. 2020 Oct;2(10):e549-e560.
doi: 10.1016/S2589-7500(20)30219-3. Epub 2020 Sep 9.

Guidelines for clinical trial protocols for interventions involving artificial intelligence: the SPIRIT-AI extension

Collaborators, Affiliations
Review

Guidelines for clinical trial protocols for interventions involving artificial intelligence: the SPIRIT-AI extension

Samantha Cruz Rivera et al. Lancet Digit Health. 2020 Oct.

Abstract

The SPIRIT 2013 statement aims to improve the completeness of clinical trial protocol reporting by providing evidence-based recommendations for the minimum set of items to be addressed. This guidance has been instrumental in promoting transparent evaluation of new interventions. More recently, there has been a growing recognition that interventions involving artificial intelligence (AI) need to undergo rigorous, prospective evaluation to demonstrate their impact on health outcomes. The SPIRIT-AI (Standard Protocol Items: Recommendations for Interventional Trials-Artificial Intelligence) extension is a new reporting guideline for clinical trial protocols evaluating interventions with an AI component. It was developed in parallel with its companion statement for trial reports: CONSORT-AI (Consolidated Standards of Reporting Trials-Artificial Intelligence). Both guidelines were developed through a staged consensus process involving literature review and expert consultation to generate 26 candidate items, which were consulted upon by an international multi-stakeholder group in a two-stage Delphi survey (103 stakeholders), agreed upon in a consensus meeting (31 stakeholders) and refined through a checklist pilot (34 participants). The SPIRIT-AI extension includes 15 new items that were considered sufficiently important for clinical trial protocols of AI interventions. These new items should be routinely reported in addition to the core SPIRIT 2013 items. SPIRIT-AI recommends that investigators provide clear descriptions of the AI intervention, including instructions and skills required for use, the setting in which the AI intervention will be integrated, considerations for the handling of input and output data, the human-AI interaction and analysis of error cases. SPIRIT-AI will help promote transparency and completeness for clinical trial protocols for AI interventions. Its use will assist editors and peer reviewers, as well as the general readership, to understand, interpret, and critically appraise the design and risk of bias for a planned clinical trial.

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Conflict of interest statement

Declaration of interests

MJC has received personal fees from Astellas, Takeda, Merck, Daiichi Sankyo, Glaukos, GlaxoSmithKline, and the Patient-Centered Outcomes Research Institute (PCORI), outside the submitted work. ADa is an advisor for Google DeepMind, outside the submitted work. LF reports personal fees from Allergan, Bayer, and Novartis, outside the submitted work. JF reports personal fees from British Medical Journal, during the conduct of the study. HH reports that he is Managing Director at Hardian Health, consultancy for health technology firms. PAK reports personal fees from DeepMind Technologies, Roche, Novartis, Apellis, Bayer, Allergan, Topcon, and Heidelberg Engineering, outside the submitted work. AYL reports personal fees from Genentech, US Food and Drug Administration, and Verana Health, grants from Microsoft, NVIDIA, Carl Zeiss Meditec, and Santen, outside the submitted work. CSL reports grants from National Institute of Health/National Institute on Aging, outside the submitted work. CJK is an employee of Google and owns Alphabet stock. AE is an employee of Salesforce CRM. RiS is an employee of Pinpoint Science. JMa was an employee of AstraZeneca PLC at the time of this study. RuS is Editor-in-Chief of The Lancet Digital Health and reports personal fees from The Lancet Group, during the conduct of the study. JMo is Chief Editor of the journal Nature Medicine; he has recused himself from any aspect of decision-making on this manuscript and played no part in the assignment of this manuscript to in-house editors or peer reviewers, and was also separated and blinded from the editorial process from submission inception to decision. SJV reports funding from IQVIA. All other authors declare no competing interests.

Figures

Figure 1:
Figure 1:. SPIRIT-AI checklist
aIt is strongly recommended that this checklist be read in conjunction with the SPIRIT 2013 Explanation & Elaboration for important clarification on the items. bIndicates page numbers to be completed by authors during protocol development.
Figure 1:
Figure 1:. SPIRIT-AI checklist
aIt is strongly recommended that this checklist be read in conjunction with the SPIRIT 2013 Explanation & Elaboration for important clarification on the items. bIndicates page numbers to be completed by authors during protocol development.
Figure 1:
Figure 1:. SPIRIT-AI checklist
aIt is strongly recommended that this checklist be read in conjunction with the SPIRIT 2013 Explanation & Elaboration for important clarification on the items. bIndicates page numbers to be completed by authors during protocol development.
Figure 1:
Figure 1:. SPIRIT-AI checklist
aIt is strongly recommended that this checklist be read in conjunction with the SPIRIT 2013 Explanation & Elaboration for important clarification on the items. bIndicates page numbers to be completed by authors during protocol development.
Figure 1:
Figure 1:. SPIRIT-AI checklist
aIt is strongly recommended that this checklist be read in conjunction with the SPIRIT 2013 Explanation & Elaboration for important clarification on the items. bIndicates page numbers to be completed by authors during protocol development.
Figure 2:
Figure 2:. CONSORT 2010 flow diagram, adapted for AI clinical trials
AI=artificial intelligence. SPIRIT-AI 10 (i): State the inclusion and exclusion criteria at the level of participants. SPIRIT-AI 10 (ii): State the inclusion and exclusion criteria at the level of the input data. SPIRIT 13 (core CONSORT item): Time schedule of enrollment, interventions (including any run-ins and washouts), assessments, and visits for participants. A schematic diagram is highly recommended.

References

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