Literature DB >> 20848576

Determining the minimum clinically important differences for outcomes in the DOMINO trial.

Robert Howard1, Patrick Phillips, Tony Johnson, John O'Brien, Bart Sheehan, James Lindesay, Peter Bentham, Alistair Burns, Clive Ballard, Clive Holmes, Ian McKeith, Robert Barber, Tom Dening, Craig Ritchie, Rob Jones, Ashley Baldwin, Peter Passmore, David Findlay, Alan Hughes, Ajay Macharouthu, Sube Banerjee, Roy Jones, Martin Knapp, Richard G Brown, Robin Jacoby, Jessica Adams, Mary Griffin, Richard Gray.   

Abstract

BACKGROUND: Although less likely to be reported in clinical trials than expressions of the statistical significance of differences in outcomes, whether or not a treatment has delivered a specified minimum clinically important difference (MCID) is also relevant to patients and their caregivers and doctors. Many dementia treatment randomised controlled trials (RCTs) have not reported MCIDs and, where they have been done, observed differences have not reached these.
METHODS: As part of the development of the Statistical Analysis Plan for the DOMINO trial, investigators met to consider expert opinion- and distribution-based values for the MCID and triangulated these to provide appropriate values for three outcome measures, the Standardised Mini-mental State Examination (sMMSE), Bristol Activities of Daily Living Scale (BADLS) and Neuropsychiatric Inventory (NPI). Only standard deviations (SD) were presented to investigators who remained blind to treatment allocation.
RESULTS: Adoption of values for MCIDs based upon 0.4 of the SD of the change in score from baseline on the sMMSE, BADLS and NPI in the first 127 participants to complete DOMINO yielded MCIDs of 1.4 points for sMMSE, 3.5 for BADLS and 8.0 for NPI.
CONCLUSIONS: Reference to MCIDs is important for the full interpretation of the results of dementia trials and those conducting such trials should be open about the way in which they have determined and chosen their values for the MCIDs.
Copyright © 2010 John Wiley & Sons, Ltd.

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Year:  2010        PMID: 20848576     DOI: 10.1002/gps.2607

Source DB:  PubMed          Journal:  Int J Geriatr Psychiatry        ISSN: 0885-6230            Impact factor:   3.485


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