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However, peripheral nerve stimulation using\n                      <jats:styled-content style=\"fixed-case\">TENS<\/jats:styled-content>\n                      can alter muscle motor output. Few studies examine motor outcomes following\n                      <jats:styled-content style=\"fixed-case\">TENS<\/jats:styled-content>\n                      in a human pain model. Therefore, this study investigated the influence of\n                      <jats:styled-content style=\"fixed-case\">TENS<\/jats:styled-content>\n                      sensory stimulation primarily on motor output (strength) and secondarily on pain and disability following exercise\u2010induced delayed\u2010onset muscle soreness (\n                      <jats:styled-content style=\"fixed-case\">DOMS<\/jats:styled-content>\n                      ).\n                    <\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec>\n                    <jats:title>Methods<\/jats:title>\n                    <jats:p>\n                      Thirty\u2010six participants were randomized to a\n                      <jats:styled-content style=\"fixed-case\">TENS<\/jats:styled-content>\n                      treatment,\n                      <jats:styled-content style=\"fixed-case\">TENS<\/jats:styled-content>\n                      placebo, or control group after completing a standardized\n                      <jats:styled-content style=\"fixed-case\">DOMS<\/jats:styled-content>\n                      protocol. Measures included shoulder strength, pain, mechanical pain sensitivity, and disability.\n                      <jats:styled-content style=\"fixed-case\">TENS<\/jats:styled-content>\n                      treatment and\n                      <jats:styled-content style=\"fixed-case\">TENS<\/jats:styled-content>\n                      placebo groups received 90\u00a0minutes of active or sham treatment 24, 48, and 72\u00a0hours post\u2010\n                      <jats:styled-content style=\"fixed-case\">DOMS<\/jats:styled-content>\n                      . All participants were assessed daily.\n                    <\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec>\n                    <jats:title>Results<\/jats:title>\n                    <jats:p>\n                      A repeated measures analysis of variance and post\u2010hoc analysis indicated that, compared to the control group, strength remained reduced in the\n                      <jats:styled-content style=\"fixed-case\">TENS<\/jats:styled-content>\n                      treatment group (48\u00a0hours post\u2010\n                      <jats:styled-content style=\"fixed-case\">DOMS<\/jats:styled-content>\n                      ,\n                      <jats:italic>P\u00a0<\/jats:italic>\n                      &lt;\n                      <jats:italic>\u00a0<\/jats:italic>\n                      0.05) and\n                      <jats:styled-content style=\"fixed-case\">TENS<\/jats:styled-content>\n                      placebo group (48\u00a0hours post\u2010\n                      <jats:styled-content style=\"fixed-case\">DOMS<\/jats:styled-content>\n                      ,\n                      <jats:italic>P\u00a0<\/jats:italic>\n                      &lt;\n                      <jats:italic>\u00a0<\/jats:italic>\n                      0.05; 72\u00a0hours post\u2010\n                      <jats:styled-content style=\"fixed-case\">DOMS<\/jats:styled-content>\n                      ,\n                      <jats:italic>P\u00a0<\/jats:italic>\n                      &lt;\n                      <jats:italic>\u00a0<\/jats:italic>\n                      0.05). A mixed\u2010linear modeling analysis was conducted to examine the strength (motor) change. Randomization group explained 5.6% of between\u2010subject strength variance (\n                      <jats:italic>P\u00a0<\/jats:italic>\n                      &lt;\n                      <jats:italic>\u00a0<\/jats:italic>\n                      0.05). Independent of randomization group, pain explained 8.9% of within\u2010subject strength variance and disability explained 3.3% of between\u2010subject strength variance (both\n                      <jats:italic>P\u00a0<\/jats:italic>\n                      &lt;\n                      <jats:italic>\u00a0<\/jats:italic>\n                      0.05).\n                    <\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec>\n                    <jats:title>Discussion<\/jats:title>\n                    <jats:p>\n                      While active and placebo\n                      <jats:styled-content style=\"fixed-case\">TENS<\/jats:styled-content>\n                      resulted in prolonged strength inhibition, the results were nonsignificant for pain. Results indicated that higher pain and higher disability were independently related to decreased strength. Regardless of the impact on pain,\n                      <jats:styled-content style=\"fixed-case\">TENS<\/jats:styled-content>\n                      , or even the perception of\n                      <jats:styled-content style=\"fixed-case\">TENS<\/jats:styled-content>\n                      , may act as a nocebo for motor output.\n                    <\/jats:p>\n                  <\/jats:sec>","DOI":"10.1111\/papr.12690","type":"journal-article","created":{"date-parts":[[2018,3,5]],"date-time":"2018-03-05T12:38:00Z","timestamp":1520253480000},"page":"954-968","update-policy":"https:\/\/doi.org\/10.1002\/crossmark_policy","source":"Crossref","is-referenced-by-count":7,"title":["Prolonged Reduction in Shoulder Strength after Transcutaneous Electrical Nerve Stimulation Treatment of Exercise\u2010Induced Acute Muscle Pain"],"prefix":"10.1111","volume":"18","author":[{"given":"Katie A.","family":"Butera","sequence":"first","affiliation":[{"name":"Department of Physical Therapy 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