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Transcutaneous electrical nerve stimulation (\n                      <jats:styled-content style=\"fixed-case\">TENS<\/jats:styled-content>\n                      ) activates endogenous pain inhibitory mechanisms. This study was undertaken to investigate if using\n                      <jats:styled-content style=\"fixed-case\">TENS<\/jats:styled-content>\n                      during activity would improve movement\u2010evoked pain and other patient\u2010reported outcomes in women with\n                      <jats:styled-content style=\"fixed-case\">FM<\/jats:styled-content>\n                      .\n                    <\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec>\n                    <jats:title>Methods<\/jats:title>\n                    <jats:p>\n                      Participants were randomly assigned to receive active\n                      <jats:styled-content style=\"fixed-case\">TENS<\/jats:styled-content>\n                      (n = 103), placebo\n                      <jats:styled-content style=\"fixed-case\">TENS<\/jats:styled-content>\n                      (n = 99), or no\n                      <jats:styled-content style=\"fixed-case\">TENS<\/jats:styled-content>\n                      (n = 99) and instructed to use it at home during activity 2 hours each day for 4 weeks.\n                      <jats:styled-content style=\"fixed-case\">TENS<\/jats:styled-content>\n                      was applied to the lumbar and cervicothoracic regions using a modulated frequency (2\u2013125 Hz) at the highest tolerable intensity. Participants rated movement\u2010evoked pain (primary outcome measure) and fatigue on an 11\u2010point scale before and during application of\n                      <jats:styled-content style=\"fixed-case\">TENS<\/jats:styled-content>\n                      . The primary outcome measure and secondary patient\u2010reported outcomes were assessed at baseline (time of randomization) and at 4 weeks.\n                    <\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec>\n                    <jats:title>Results<\/jats:title>\n                    <jats:p>\n                      After 4 weeks, a greater reduction in movement\u2010evoked pain was reported in the active\n                      <jats:styled-content style=\"fixed-case\">TENS<\/jats:styled-content>\n                      group versus the placebo\n                      <jats:styled-content style=\"fixed-case\">TENS<\/jats:styled-content>\n                      group (group mean difference \u20131.0 [95% confidence interval \u20131.8, \u20130.2];\n                      <jats:italic>P<\/jats:italic>\n                      = 0.008) and versus the no\n                      <jats:styled-content style=\"fixed-case\">TENS<\/jats:styled-content>\n                      group (group mean difference \u20131.8 [95% confidence interval \u20132.6, \u20131.0];\n                      <jats:italic>P<\/jats:italic>\n                      &lt; 0.0001). A reduction in movement\u2010evoked fatigue was also reported in the active\n                      <jats:styled-content style=\"fixed-case\">TENS<\/jats:styled-content>\n                      group versus the placebo\n                      <jats:styled-content style=\"fixed-case\">TENS<\/jats:styled-content>\n                      group (group mean difference \u20131.4 [95% confidence interval \u20132.4, \u20130.4];\n                      <jats:italic>P<\/jats:italic>\n                      = 0.001) and versus the no\n                      <jats:styled-content style=\"fixed-case\">TENS<\/jats:styled-content>\n                      group (group mean difference \u20131.9 [95% confidence interval \u20132.9, \u20130.9];\n                      <jats:italic>P<\/jats:italic>\n                      = &lt;0.0001). A greater percentage of the patients in the active\n                      <jats:styled-content style=\"fixed-case\">TENS<\/jats:styled-content>\n                      group reported improvement on the global impression of change compared to the placebo\n                      <jats:styled-content style=\"fixed-case\">TENS<\/jats:styled-content>\n                      group (70% versus 31%;\n                      <jats:italic>P<\/jats:italic>\n                      &lt; 0.0001) and the no\n                      <jats:styled-content style=\"fixed-case\">TENS<\/jats:styled-content>\n                      group (9%;\n                      <jats:italic>P<\/jats:italic>\n                      &lt; 0.0001). There were no\n                      <jats:styled-content style=\"fixed-case\">TENS<\/jats:styled-content>\n                      \u2010related serious adverse events, and &lt;5% of participants experienced minor adverse events from\n                      <jats:styled-content style=\"fixed-case\">TENS<\/jats:styled-content>\n                      .\n                    <\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec>\n                    <jats:title>Conclusion<\/jats:title>\n                    <jats:p>\n                      Among women who had\n                      <jats:styled-content style=\"fixed-case\">FM<\/jats:styled-content>\n                      and were on a stable medication regimen, 4 weeks of active\n                      <jats:styled-content style=\"fixed-case\">TENS<\/jats:styled-content>\n                      use compared to placebo\n                      <jats:styled-content style=\"fixed-case\">TENS<\/jats:styled-content>\n                      or no\n                      <jats:styled-content style=\"fixed-case\">TENS<\/jats:styled-content>\n                      resulted in a significant improvement in movement\u2010evoked pain and other clinical outcomes. Further research is needed to examine effectiveness in a real\u2010world setting to establish the clinical importance of these findings.\n                    <\/jats:p>\n                  <\/jats:sec>","DOI":"10.1002\/art.41170","type":"journal-article","created":{"date-parts":[[2019,11,18]],"date-time":"2019-11-18T08:28:30Z","timestamp":1574065710000},"page":"824-836","update-policy":"https:\/\/doi.org\/10.1002\/crossmark_policy","source":"Crossref","is-referenced-by-count":103,"title":["Transcutaneous Electrical Nerve Stimulation Reduces Movement\u2010Evoked Pain and Fatigue: A Randomized, Controlled Trial"],"prefix":"10.1002","volume":"72","author":[{"given":"Dana L.","family":"Dailey","sequence":"first","affiliation":[{"name":"University of Iowa, Iowa City, and St. Ambrose University  Davenport Iowa"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Carol G. 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