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This randomised controlled clinical trial included 40 patients who were clinically diagnosed with myofascial pain according to Research Diagnostic Criteria for Temporomandibular Disorders (<jats:styled-content style=\"fixed-case\">RDC<\/jats:styled-content>\/<jats:styled-content style=\"fixed-case\">TMD<\/jats:styled-content>). Patients were randomly divided into two groups: the first group comprised patients who received guidance, assurance, counselling and behavioural changes; an <jats:styled-content style=\"fixed-case\">NTI<\/jats:styled-content>\u2010tss device was integrated to this protocol in the second group. Both groups exhibited reduction in pain levels and improvement of jaw function compared with baseline values, but the difference was not significant. Both groups demonstrated improvements in 6 weeks; however, the integration of <jats:styled-content style=\"fixed-case\">NTI<\/jats:styled-content>\u2010tss device into the therapy protocol did not provide any additional benefit in relieving symptoms of myofascial pain.<\/jats:p>","DOI":"10.1111\/joor.12524","type":"journal-article","created":{"date-parts":[[2017,5,18]],"date-time":"2017-05-18T15:59:48Z","timestamp":1495123188000},"page":"589-593","source":"Crossref","is-referenced-by-count":22,"title":["Can an <scp>NTI<\/scp>\u2010tss device be effective as a first\u2010line therapy in patients with <scp>TMD<\/scp> myofascial pain?"],"prefix":"10.1111","volume":"44","author":[{"ORCID":"https:\/\/orcid.org\/0000-0003-0743-199X","authenticated-orcid":false,"given":"G. 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