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MOESM1 of How to help researchers in palliative care improve responsiveness to migrants and other underrepresented populations: developing and testing a self-assessment instrument

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posted on 2019-10-22, 19:04 authored by M. Torensma, B. Onwuteaka-Philipsen, K. Strackee, M. Oosterveld-Vlug, X. Voogd, D. Willems, J. Suurmond
Additional file 1. Final list of Delphi questionnaire items with mean scores and percentages. The Delphi questionnaire was established by translating the content of a pilot self-assessment instrument for diversity responsiveness in palliative care projects into a questionnaire. The questionnaire consisted of 33 items, subdivided into four sections. One section with three items on the groups included in the instrument’s focus and three sections with items on the measures from the pilot instrument according to the project stages: set-up; execution, and follow-up. The questionnaire was sent to a panel of experts who were asked to score the questionnaire items’ relevance and feasibility on a 5-point scale (1:not relevant/feasible; 5:entirely relevant/feasible). A priori set consensus rate of 75% were used, where at least 75% of the scores given by the experts should be 4 ≤ (relevance), or 3 ≤ (feasibility) in order to uphold the item in the instrument. Listed here are the final items, after revisions suggested by experts, the mean scores and consensus rate percentages.

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