Please use this identifier to cite or link to this item: http://hdl.handle.net/11328/3250
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dc.contributor.authorOhrtman, Emily A.-
dc.contributor.authorZaninotto, Ana Luiza-
dc.contributor.authorCarvalho, Sandra-
dc.contributor.authorShie, Vivian L.-
dc.contributor.authorLeite, Jorge-
dc.contributor.authorIanni, Corinne Rose-
dc.contributor.authorKazis, Lewis E.-
dc.contributor.authorRoss Zafonte, Ross Zafonte-
dc.contributor.authorRyan, Colleen M.-
dc.contributor.authorSchneider, Jeffrey C.-
dc.contributor.authorFregni, Felipe-
dc.date.accessioned2020-11-04T12:35:06Z-
dc.date.available2020-11-04T12:35:06Z-
dc.date.issued2019-
dc.identifier.citationOhrtman, E. A., Zaninotto, A. L., Carvalho, S., Shie, V. L., Leite, J., Ianni, C. R., Kazis, L. E., Zafonte, R., Ryan, C. M., Schneider, J. C., & Fregni, F. (2019). Longitudinal Clinical Trial Recruitment and Retention Challenges in the Burn Population: Lessons Learned From a Trial Examining a Novel Intervention for Chronic Neuropathic Symptoms. Journal of Burn Care & Research, 40(6), 792-795. doi: 10.1093/jbcr/irz084. Disponível no Repositório UPT, http://hdl.handle.net/11328/3250pt_PT
dc.identifier.issn1559-0488-
dc.identifier.urihttp://hdl.handle.net/11328/3250-
dc.description.abstractLong-term trials are key to understanding chronic symptoms such as pain and itch. However, challenges such as high attrition rates and poor recruitment are common when conducting research. The aim of this work was to explore these issues within a long-term randomized control trial using transcranial direct current stimulation to treat pain and itch. This parallel double blinded, placebo-controlled randomized trial was comprised of 15 transcranial direct current stimulation visits and 7 follow-up visits. Participants were over the age of 18, had a burn injury that occurred at least 3 weeks before enrollment, and reported having pain and/or itch that was moderate to severe in intensity. A total of 31 subjects were randomized into either an active or sham transcranial direct current stimulation groups. There were no significant differences between the groups in terms of age, race, education, baseline depression, or anxiety. The median dropout time was at visit 19 (visit 16 [SE = 1.98] for the sham group and visit 19 [SE = 1.98] for the active group). Analysis showed no differences in the dropout rate between groups [χ2(1) = 0.003, P = .954]. The dropout rate was 46.7% for the sham group and 43.8% for the active group. Overall, 45.2% of the subjects dropped out of the trial. Long-term clinical trials are an essential part of evaluating interventions for symptoms such as chronic pain and itch. However, as seen in this trial, long-term studies in the burn population often face recruitment and adherence challenges.pt_PT
dc.language.isoengpt_PT
dc.publisherOxford University Presspt_PT
dc.rightsopenAccesspt_PT
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/pt_PT
dc.titleLongitudinal Clinical Trial Recruitment and Retention Challenges in the Burn Population: Lessons Learned from a Trial Examining a Novel Intervention for Chronic Neuropathic Symptomspt_PT
dc.typearticlept_PT
dc.relation.publisherversionhttps://pubmed.ncbi.nlm.nih.gov/31102438/pt_PT
dc.peerreviewedyespt_PT
degois.publication.firstPage792pt_PT
degois.publication.lastPage795pt_PT
degois.publication.volume40pt_PT
degois.publication.issue6pt_PT
degois.publication.titleJournal of Burn Care & Researchpt_PT
degois.publication.locationUSApt_PT
dc.identifier.doi10.1093/jbcr/irz084pt_PT
Appears in Collections:INPP - Artigos em Revistas Internacionais / Papers in International Journals

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