{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,10,8]],"date-time":"2026-10-08T14:02:25Z","timestamp":1791468145207,"version":"4.3.4"},"reference-count":51,"publisher":"Wiley","issue":"10","license":[{"start":{"date-parts":[[2014,5,13]],"date-time":"2014-05-13T00:00:00Z","timestamp":1399939200000},"content-version":"vor","delay-in-days":0,"URL":"http:\/\/creativecommons.org\/licenses\/by-nc-nd\/3.0\/"}],"funder":[{"DOI":"10.13039\/501100005416","name":"Norwegian Research Council","doi-asserted-by":"crossref","award":["protocol code 189439"],"award-info":[{"award-number":["protocol code 189439"]}],"id":[{"id":"10.13039\/501100005416","id-type":"DOI","asserted-by":"crossref"}]}],"content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":["European Journal of Pain"],"published-print":{"date-parts":[[2014,11]]},"abstract":"<jats:title>Abstract<\/jats:title>\n                  <jats:sec>\n                    <jats:title>Background<\/jats:title>\n                    <jats:p>Pain is frequent and distressing in people with dementia, but no randomized controlled trials have evaluated the effect of analgesic treatment on pain intensity as a key outcome.<\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec>\n                    <jats:title>Methods<\/jats:title>\n                    <jats:p>\n                      Three hundred fifty\u2010two people with dementia and significant agitation from 60 nursing home units were included in this study. These units, representing 18 nursing homes in western\n                      <jats:styled-content style=\"fixed-case\">N<\/jats:styled-content>\n                      orway, were randomized to a stepwise protocol of treating pain (\n                      <jats:styled-content style=\"fixed-case\">SPTP<\/jats:styled-content>\n                      ) or usual care. The\n                      <jats:styled-content style=\"fixed-case\">SPTP<\/jats:styled-content>\n                      group received acetaminophen, morphine, buprenorphine transdermal patch and pregabalin for 8 weeks, with a 4\u2010week washout period. Medications were governed by the\n                      <jats:styled-content style=\"fixed-case\">SPTP<\/jats:styled-content>\n                      and each participant's existing prescriptions. We obtained pain intensity scores from 327 patients (intervention\n                      <jats:italic>n<\/jats:italic>\n                      \u2009=\u2009164, control\n                      <jats:italic>n<\/jats:italic>\n                      \u2009=\u2009163) at five time points assessed by the primary outcome measure, Mobilization\u2010Observation\u2010Behaviour\u2010Intensity\u2010Dementia\u20102 (\n                      <jats:styled-content style=\"fixed-case\">MOBID<\/jats:styled-content>\n                      \u20102) Pain Scale. The secondary outcome was activities of daily living (\n                      <jats:styled-content style=\"fixed-case\">ADL<\/jats:styled-content>\n                      ). We used a linear intercept mixed model in a two\u2010way repeated measures configuration to assess change over time and between groups.\n                    <\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec>\n                    <jats:title>Results<\/jats:title>\n                    <jats:p>\n                      The\n                      <jats:styled-content style=\"fixed-case\">SPTP<\/jats:styled-content>\n                      conferred significant benefit in\n                      <jats:styled-content style=\"fixed-case\">MOBID<\/jats:styled-content>\n                      \u20102 scores compared with the control group [average treatment effect (\n                      <jats:styled-content style=\"fixed-case\">ATE<\/jats:styled-content>\n                      ) \u22121.388;\n                      <jats:italic>p<\/jats:italic>\n                      \u2009&lt;\u20090.001] at week 8, and\n                      <jats:styled-content style=\"fixed-case\">MOBID<\/jats:styled-content>\n                      \u20102 scores worsened during the washout period (\n                      <jats:styled-content style=\"fixed-case\">ATE<\/jats:styled-content>\n                      \u2009=\u2009\u22120.701;\n                      <jats:italic>p<\/jats:italic>\n                      \u2009=\u20090.022). Examining different analgesic treatments, benefit was conferred to patients receiving acetaminophen compared with the controls at week 2 (\n                      <jats:styled-content style=\"fixed-case\">ATE<\/jats:styled-content>\n                      \u2009=\u2009\u22120.663;\n                      <jats:italic>p<\/jats:italic>\n                      \u2009=\u20090.010), continuing to increase until week 8 (\n                      <jats:styled-content style=\"fixed-case\">ATE<\/jats:styled-content>\n                      \u2009=\u2009\u22121.297;\n                      <jats:italic>p<\/jats:italic>\n                      \u2009&lt;\u20090.001). Although there were no overall improvements in\n                      <jats:styled-content style=\"fixed-case\">ADL<\/jats:styled-content>\n                      , an increase was seen in the group receiving acetaminophen (\n                      <jats:styled-content style=\"fixed-case\">ATE<\/jats:styled-content>\n                      \u2009=\u2009+1.0;\n                      <jats:italic>p<\/jats:italic>\n                      \u2009=\u20090.022).\n                    <\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec>\n                    <jats:title>Conclusion<\/jats:title>\n                    <jats:p>\n                      Pain medication significantly improved pain in the intervention group, with indications that acetaminophen also improved\n                      <jats:styled-content style=\"fixed-case\">ADL<\/jats:styled-content>\n                      function.\n                    <\/jats:p>\n                  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