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Psychophysiologic Symptom Relief Therapy for Post-Acute Sequelae of Coronavirus Disease 2019
OBJECTIVE: To determine if psychophysiologic symptom relief therapy (PSRT) will reduce symptom burden in patients suffering from post-acute sequelae of coronavirus disease 2019 (COVID-19) (PASC) who had mild/moderate acute COVID-19 disease without objective evidence of organ injury. PATIENTS AND MET...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10196153/ https://www.ncbi.nlm.nih.gov/pubmed/37361483 http://dx.doi.org/10.1016/j.mayocpiqo.2023.05.002 |
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author | Donnino, Michael Howard, Patricia Mehta, Shivani Silverman, Jeremy Cabrera, Maria J. Yamin, Jolin B. Balaji, Lakshman Berg, Katherine M. Heydrick, Stanley Edwards, Robert Grossestreuer, Anne V. |
author_facet | Donnino, Michael Howard, Patricia Mehta, Shivani Silverman, Jeremy Cabrera, Maria J. Yamin, Jolin B. Balaji, Lakshman Berg, Katherine M. Heydrick, Stanley Edwards, Robert Grossestreuer, Anne V. |
author_sort | Donnino, Michael |
collection | PubMed |
description | OBJECTIVE: To determine if psychophysiologic symptom relief therapy (PSRT) will reduce symptom burden in patients suffering from post-acute sequelae of coronavirus disease 2019 (COVID-19) (PASC) who had mild/moderate acute COVID-19 disease without objective evidence of organ injury. PATIENTS AND METHODS: Twenty-three adults under the age of 60 years with PASC for at least 12 weeks after COVID-19 infection were enrolled in an interventional cohort study conducted via a virtual platform between May 18, 2021 and August 7, 2022. Participants received PSRT during a 13-week (approximately 44-hour) course. Participants were administered validated questionnaires at baseline and at 4, 8, and 13 weeks. The primary outcome was a change in somatic symptoms from baseline, measured using the Somatic Symptom Scale-8, at 13 weeks. RESULTS: The median duration of symptoms before joining the study was 267 days (interquartile range: 144, 460). The mean Somatic Symptom Scale-8 score of the cohort decreased from baseline by 8.5 (95% CI: 5.7-11.4), 9.4 (95% CI: 6.9-11.9), and 10.9 (95% CI: 8.3-13.5) at 4, 8, and 13 weeks, respectively (all P<.001). Participants also experienced statistically significant improvements across other secondary outcomes including changes in dyspnea, fatigue, and pain (all P<.001). CONCLUSION: PSRT may effectively decrease symptom burden in patients suffering from PASC without evidence of organ injury. The study was registered on clinicaltrials.gov |
format | Online Article Text |
id | pubmed-10196153 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
spelling | pubmed-101961532023-05-19 Psychophysiologic Symptom Relief Therapy for Post-Acute Sequelae of Coronavirus Disease 2019 Donnino, Michael Howard, Patricia Mehta, Shivani Silverman, Jeremy Cabrera, Maria J. Yamin, Jolin B. Balaji, Lakshman Berg, Katherine M. Heydrick, Stanley Edwards, Robert Grossestreuer, Anne V. Mayo Clin Proc Innov Qual Outcomes Original Article OBJECTIVE: To determine if psychophysiologic symptom relief therapy (PSRT) will reduce symptom burden in patients suffering from post-acute sequelae of coronavirus disease 2019 (COVID-19) (PASC) who had mild/moderate acute COVID-19 disease without objective evidence of organ injury. PATIENTS AND METHODS: Twenty-three adults under the age of 60 years with PASC for at least 12 weeks after COVID-19 infection were enrolled in an interventional cohort study conducted via a virtual platform between May 18, 2021 and August 7, 2022. Participants received PSRT during a 13-week (approximately 44-hour) course. Participants were administered validated questionnaires at baseline and at 4, 8, and 13 weeks. The primary outcome was a change in somatic symptoms from baseline, measured using the Somatic Symptom Scale-8, at 13 weeks. RESULTS: The median duration of symptoms before joining the study was 267 days (interquartile range: 144, 460). The mean Somatic Symptom Scale-8 score of the cohort decreased from baseline by 8.5 (95% CI: 5.7-11.4), 9.4 (95% CI: 6.9-11.9), and 10.9 (95% CI: 8.3-13.5) at 4, 8, and 13 weeks, respectively (all P<.001). Participants also experienced statistically significant improvements across other secondary outcomes including changes in dyspnea, fatigue, and pain (all P<.001). CONCLUSION: PSRT may effectively decrease symptom burden in patients suffering from PASC without evidence of organ injury. The study was registered on clinicaltrials.gov Elsevier 2023-05-19 /pmc/articles/PMC10196153/ /pubmed/37361483 http://dx.doi.org/10.1016/j.mayocpiqo.2023.05.002 Text en © 2023 Published by Elsevier Inc on behalf of Mayo Foundation for Medical Education and Research. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/). |
spellingShingle | Original Article Donnino, Michael Howard, Patricia Mehta, Shivani Silverman, Jeremy Cabrera, Maria J. Yamin, Jolin B. Balaji, Lakshman Berg, Katherine M. Heydrick, Stanley Edwards, Robert Grossestreuer, Anne V. Psychophysiologic Symptom Relief Therapy for Post-Acute Sequelae of Coronavirus Disease 2019 |
title | Psychophysiologic Symptom Relief Therapy for Post-Acute Sequelae of Coronavirus Disease 2019 |
title_full | Psychophysiologic Symptom Relief Therapy for Post-Acute Sequelae of Coronavirus Disease 2019 |
title_fullStr | Psychophysiologic Symptom Relief Therapy for Post-Acute Sequelae of Coronavirus Disease 2019 |
title_full_unstemmed | Psychophysiologic Symptom Relief Therapy for Post-Acute Sequelae of Coronavirus Disease 2019 |
title_short | Psychophysiologic Symptom Relief Therapy for Post-Acute Sequelae of Coronavirus Disease 2019 |
title_sort | psychophysiologic symptom relief therapy for post-acute sequelae of coronavirus disease 2019 |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10196153/ https://www.ncbi.nlm.nih.gov/pubmed/37361483 http://dx.doi.org/10.1016/j.mayocpiqo.2023.05.002 |
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