How to use the Harmonising Outcome Measures for Eczema Core Outcome Set for atopic dermatitis trials: a users’ guide

Author:

Thomas Kim S1ORCID,Howells Laura1ORCID,Leshem Yael A23ORCID,Simpson Eric L4,Apfelbacher Christian56ORCID,Spuls Phyllis I7,Gerbens Louise A A7,Jacobson Michael E4ORCID,Katoh Norito8,Williams Hywel C1,Stuart Beth L9

Affiliation:

1. Centre of Evidence Based Dermatology, School of Medicine, University of Nottingham , Nottingham , UK

2. Division of Dermatology, Rabin Medical Center , Petach-Tikva , Israel

3. School of Medicine, Tel-Aviv University , Tel-Aviv , Israel

4. Department of Dermatology, Oregon Health and Science University , Portland, OR , USA

5. Institute of Social Medicine and Health Systems Research, Otto von Guericke University Magdeburg , Magdeburg , Germany

6. Lee Kong Chian School of Medicine, Nanyang Technological University Singapore , Singapore

7. Department of Dermatology, Amsterdam UMC, location Academic Medical Center, University of Amsterdam, Amsterdam Public Health, Infection and Immunity , Amsterdam , the Netherlands

8. Department of Dermatology, Kyoto Prefectural University of Medicine , Kyoto , Japan

9. Wolfston Institute of Population Health, Queen Mary University of London , London , UK

Abstract

Abstract Background The Harmonising Outcome Measures for Eczema (HOME) initiative has agreed upon the Core Outcome Set (COS) for use in atopic dermatitis (AD) clinical trials, but additional guidance is needed to maximize its uptake. Objectives To provide answers to some of the commonly asked questions about using the HOME COS; to provide data to help with the interpretation of trial results; and to support sample size calculations for future trials. Methods and results We provide practical guidance on the use of the HOME COS for investigators planning clinical trials in patients with AD. It answers some of the common questions about using the HOME COS, how to access the outcome measurement instruments, what training/resources are needed to use them appropriately and clarifies when the COS is applicable. We also provide exemplar data to inform sample size calculations for eczema trials and encourage standardized data collection and reporting of the COS. Conclusions By encouraging adoption of the COS and facilitating consistent reporting of outcome data, it is hoped that the results of eczema trials will be more comprehensive and readily combined in meta-analyses and that patient care will subsequently be improved.

Publisher

Oxford University Press (OUP)

Subject

Dermatology

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