Skip to content

Advertisement

  • Poster presentation
  • Open Access

TINNET COST Action BM1306: an international standard for outcome measurements in clinical trials of tinnitus

Trials201516 (Suppl 1) :P18

https://doi.org/10.1186/1745-6215-16-S1-P18

  • Published:

Keywords

  • Cost Action
  • Consensus Meeting
  • Survey Methodology
  • Outcome Domain
  • Delphi Survey

Background

Over 70 million people in Europe experience tinnitus, for 7 million it creates a debilitating condition. In spite of its enormous socioeconomic relevance, research funding is somewhat limited. The European Union has approved funding for a COST Action TINNET (2014-2018) to create a pan-European tinnitus research network. One of the Working Groups will address outcome measurement; building upon the 2006 consensus meeting organised by the Tinnitus Research Initiative [1]. This Working Group seeks to embrace inclusivity and brings together clinicians, experts on clinical research methodology, statisticians, and representatives of the health industry. The primary objective is to establish an international standard for outcome measurements in clinical trials of tinnitus.

Methods

The first step towards the objective is to seek a consensus about appropriate and relevant outcome domains, using Delphi survey methodology. Details of the study design and collaborative approach will be confirmed at the first Working Group management team on November 14th. On November 13th, we are also holding a COST Action workshop in Amsterdam, “Agreed Standards for Measurement : An International Perspective” with invited talks on the COSMIN and the HOME initiatives, and the World Health Organisation International Classification of Functioning, Disability and Health (ICF) core sets for assessment of hearing loss.

Conclusion

Once our methodology is confirmed we will register our work on the COMET database. Furthermore, by working with the COST Action Clinical and Database Working Groups we can achieve standards for outcome measurement both in clinical trials and in clinical routine and support data collection of treatment results in a centralised database.

Declarations

Acknowledgements

Winifred Schlee (Action Chair), University Hospital Regensburg, Germany, on behalf of all participants of the EU COST Action BM1306.

Alain Londero (Working Group co-chair) Hôpital Européen Georges-Pompidou, Paris 5 University, France.

Authors’ Affiliations

(1)
National Institute for Health Research (NIHR) Nottingham Hearing Biomedical Research Unit, Nottingham, NG1 5DU, UK
(2)
University of Nottingham, NG7 2RD, UK
(3)
Hôpital Européen Georges-Pompidou, Paris 5 University, France

References

  1. Langguth B, Goodey R, Azevedo A, et al: Consensus for tinnitus patient assessment and treatment outcome measurement: Tinnitus Research Initiative meeting, Regensburg, July 2006. Progress in Brain Research. 2007, 166: 525-536.View ArticlePubMedPubMed CentralGoogle Scholar

Copyright

© Hall et al; licensee BioMed Central Ltd. 2015

This article is published under license to BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.

Comments

By submitting a comment you agree to abide by our Terms and Community Guidelines. If you find something abusive or that does not comply with our terms or guidelines please flag it as inappropriate. Please note that comments may be removed without notice if they are flagged by another user or do not comply with our community guidelines.

Advertisement