THE DEVELOPMENT AND VALIDATION OF A QUALITY OF LIFE MEASURE FOR PEOPLE WITH MILD COGNITIVE IMPAIRMENT (THE MCQ)
Author(s)
Dean K1;Walker Z2;Churchman D*3;Wilcock G4, Jenkinson C4 1Royal Berkshire NHS Foundation Trust, London, United Kingdom, 2University College London, London, United Kingdom, 3Isis Outcomes, Oxford, United Kingdom, 4University of Oxford, Oxford, United Kingdom
OBJECTIVES: Mild cognitive impairment (MCI) is a state that lies between normal cognition and dementia, and the number of cases with the condition is rising as the population ages. However, to date, no validated patient reported outcome measure (PRO) exists specifically in MCI. We report on a study to develop a PRO for use in MCI. METHODS: Semi-structured in-depth interviews were carried out with people with MCI in order to determine the questionnaire items. These interviews were audio-recorded, transcribed and content analysed. The draft questionnaire was refined following feedback from a focus group of patients with a diagnosis of MCI. Questionnaires were posted to subjects recruited from memory clinics and research databases, the completed questionnaires were analysed using factor analytic techniques to produce the final measure; construct validity was assessed by correlation with a generic patient reported outcome measure, the SF-12. RESULTS: Interviews were carried out with 23 people with MCI. 280 questionnaires were sent to subjects, with a response rate of 56% i.e.146 were included in the analysis. Factor analysis produced a 13 item measure tapping two domains of patient reported quality of life (‘Emotional Effects’ and ‘Practical Concerns’ ). Internal consistency reliability was high for both domains (alpha was 0.91 and 0.85 respectively). Both dimensions were found to be highly and significantly correlated with the Mental Component Summary score of the SF-12. CONCLUSIONS: The Mild Cognitive Impairment Questionnaire (MCQ) is a short 13 item measure developed specifically to measure patient reported outcomes in people with MCI. It was created on the basis of patient report, and has been shown to have good psychometric properties. It is likely to prove valuable in the evaluation of treatment regimes in this important and growing patient group.
Conference/Value in Health Info
2013-11, ISPOR Europe 2013, The Convention Centre Dublin
Value in Health, Vol. 16, No. 7 (November 2013)
Code
PMH51
Topic
Patient-Centered Research
Topic Subcategory
Patient-reported Outcomes & Quality of Life Outcomes
Disease
Mental Health