4.4 Article

The MOBID-2 pain scale: Reliability and responsiveness to pain in patients with dementia

Journal

EUROPEAN JOURNAL OF PAIN
Volume 18, Issue 10, Pages 1419-1430

Publisher

WILEY
DOI: 10.1002/ejp.507

Keywords

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Funding

  1. Norwegian Research Council [189439]
  2. University of Bergen [09/1568]

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BackgroundMobilization-Observation-Behavior-Intensity-Dementia-2 (MOBID-2) pain scale is a staff-administered pain tool for patients with dementia. This study explores MOBID-2's test-retest reliability, measurement error and responsiveness to change. MethodsAnalyses are based upon data from a cluster randomized trial including 352 patients with advanced dementia from 18 Norwegian nursing homes. Test-retest reliability between baseline and week 2 (n=163), and weeks 2 and 4 (n=159) was examined in patients not expected to change (controls), using intraclass correlation coefficient (ICC2.1), standard error of measurement (SEM) and smallest detectable change (SDC). Responsiveness was examined by testing six priori-formulated hypotheses about the association between change scores on MOBID-2 and other outcome measures. ResultsICCs of the total MOBID-2 scores were 0.81 (0-2 weeks) and 0.85 (2-4 weeks). SEM and SDC were 1.9 and 3.1 (0-2 weeks) and 1.4 and 2.3 (2-4 weeks), respectively. Five out of six hypotheses were confirmed: MOBID-2 discriminated (p<0.001) between change in patients with and without a stepwise protocol for treatment of pain (SPTP). Moderate association (r=0.35) was demonstrated with Cohen-Mansfield Agitation Inventory, and no association with Mini-Mental State Examination, Functional Assessment Staging and Activity of Daily Living. Expected associations between change scores of MOBID-2 and Neuropsychiatric Inventory - Nursing Home version were not confirmed. ConclusionThe SEM and SDC in connection with the MOBID-2 pain scale indicate that the instrument is responsive to a decrease in pain after a SPTP. Satisfactory test-retest reliability across test periods was demonstrated. Change scores3 on total and subscales are clinically relevant and are beyond measurement error.

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