dc.contributor.author
Fackrell, Kathryn
dc.contributor.author
Smith, Harriet
dc.contributor.author
Colley, Veronica
dc.contributor.author
Thacker, Brian
dc.contributor.author
Horobin, Adele
dc.contributor.author
Haider, Haula F.
dc.contributor.author
Londero, Alain
dc.contributor.author
Mazurek, Birgit
dc.contributor.author
Hall, Deborah A.
dc.date.accessioned
2018-06-08T10:42:19Z
dc.date.available
2017-10-12T07:28:20.624Z
dc.identifier.uri
https://refubium.fu-berlin.de/handle/fub188/20919
dc.identifier.uri
http://dx.doi.org/10.17169/refubium-24218
dc.description.abstract
Background The reporting of outcomes in clinical trials of subjective tinnitus
indicates that many different tinnitus-related complaints are of interest to
investigators, from perceptual attributes of the sound (e.g. loudness) to
psychosocial impacts (e.g. quality of life). Even when considering one type of
intervention strategy for subjective tinnitus, there is no agreement about
what is critically important for deciding whether a treatment is effective.
The main purpose of this observational study is, therefore to, develop Core
Outcome Domain Sets for the three different intervention strategies (sound,
psychological, and pharmacological) for adults with chronic subjective
tinnitus that should be measured and reported in every clinical trial of these
interventions. Secondary objectives are to identify the strengths and
limitations of our study design for recruiting and reducing attrition of
participants, and to explore uptake of the core outcomes. Methods The ‘Core
Outcome Measures in Tinnitus: International Delphi’ (COMIT’ID) study will use
a mixed-methods approach that incorporates input from health care users at the
pre-Delphi stage, a modified three-round Delphi survey and final consensus
meetings (one for each intervention). The meetings will generate
recommendations by stakeholder representatives on agreed Core Outcome Domain
Sets specific to each intervention. A subsequent step will establish a common
cross-cutting Core Outcome Domain Set by identifying the common outcome
domains included in all three intervention-specific Core Outcome Domain Sets.
To address the secondary objectives, we will gather feedback from participants
about their experience of taking part in the Delphi process. We aspire to
conduct an observational cohort study to evaluate uptake of the core outcomes
in published studies at 7 years following Core Outcome Set publication.
Discussion The COMIT’ID study aims to develop a Core Outcome Domain Set that
is agreed as critically important for deciding whether a treatment for
subjective tinnitus is effective. Such a recommendation would help to
standardise future clinical trials worldwide and so we will determine if
participation increases use of the Core Outcome Set in the long term. Trial
registration This project has been registered (November 2014) in the database
of the Core Outcome Measures in Effectiveness Trials (COMET) initiative.
en
dc.rights.uri
http://creativecommons.org/licenses/by/4.0/
dc.subject
Consensus methods
dc.subject
Core outcome set
dc.subject
Delphi process
dc.subject.ddc
600 Technik, Medizin, angewandte Wissenschaften::610 Medizin und Gesundheit
dc.title
Core Outcome Domains for early phase clinical trials of sound-, psychology-,
and pharmacology-based interventions to manage chronic subjective tinnitus in
adults
dc.type
Wissenschaftlicher Artikel
dc.title.subtitle
the COMIT’ID study protocol for using a Delphi process and face-to-face
meetings to establish consensus
dcterms.bibliographicCitation.doi
10.1186/s13063-017-2123-0
dcterms.bibliographicCitation.url
http://doi.org/10.1186/s13063-017-2123-0
refubium.affiliation
Charité - Universitätsmedizin Berlin
de
refubium.mycore.fudocsId
FUDOCS_document_000000028286
refubium.note.author
Der Artikel wurde in einer reinen Open-Access-Zeitschrift publiziert.
refubium.resourceType.isindependentpub
no
refubium.mycore.derivateId
FUDOCS_derivate_000000008965
dcterms.accessRights.openaire
open access