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Efficacy of the PRO-CTCAE mobile application for improving patient participation in symptom management during cancer treatment: a randomized controlled trial

PURPOSE: Although mobile-based symptom monitoring is expected to improve patient participation in symptom management during anticancer therapy, previous trials have not evaluated its effectiveness. Therefore, this study aims to evaluate the impact of a symptom monitoring mobile application on improv...

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Autores principales: Lee, Mangyeong, Kang, Danbee, Kang, Eunjee, Kim, Sooyeon, Kim, Youngha, Ahn, Jin Seok, Park, Sehhoon, Lee, Yoo-Young, Oh, Dongryul, Noh, Jae Myung, Cho, Juhee
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Berlin Heidelberg 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10163577/
https://www.ncbi.nlm.nih.gov/pubmed/37148373
http://dx.doi.org/10.1007/s00520-023-07779-3
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author Lee, Mangyeong
Kang, Danbee
Kang, Eunjee
Kim, Sooyeon
Kim, Youngha
Ahn, Jin Seok
Park, Sehhoon
Lee, Yoo-Young
Oh, Dongryul
Noh, Jae Myung
Cho, Juhee
author_facet Lee, Mangyeong
Kang, Danbee
Kang, Eunjee
Kim, Sooyeon
Kim, Youngha
Ahn, Jin Seok
Park, Sehhoon
Lee, Yoo-Young
Oh, Dongryul
Noh, Jae Myung
Cho, Juhee
author_sort Lee, Mangyeong
collection PubMed
description PURPOSE: Although mobile-based symptom monitoring is expected to improve patient participation in symptom management during anticancer therapy, previous trials have not evaluated its effectiveness. Therefore, this study aims to evaluate the impact of a symptom monitoring mobile application on improving patient participation in symptom management during anticancer therapy. METHODS: We conducted a single-center, open-label, randomized controlled trial that enrolled patients with breast, lung, head and neck, esophageal, or gynecologic cancer who were scheduled to receive anticancer therapy (oral or intravenous) between October 2020 and March 2021. We excluded patients with physical or psychological problems. The intervention group received a symptom monitoring application for 8 weeks, and the control group received the usual clinical practice. At 8 weeks, the improvement in patient participation in symptom management was assessed, and additionally quality of life and unplanned clinical visits were assessed. RESULTS: A total of 222 patients were included in the analysis, of whom 142 were randomly assigned to the intervention group and 71 to the control group. The intervention group reported better outcome in patient participation in symptom management than the control group at 8 weeks (mean scores of 8.5 vs. 8.0; P = 0.01). There were no significant differences between the groups in Quality of life (P = 0.88) and unplanned clinical visits (P = 0.39–0.76). CONCLUSIONS: This study is meaningful in figuring out that the mobile-based symptom monitoring made them more engaged in their management. Future research should continue to evaluate the effects of patient participation as mediators of clinical outcomes. TRIAL REGISTRATION: ClinicalTrials.gov NCT04568278. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s00520-023-07779-3.
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spelling pubmed-101635772023-05-09 Efficacy of the PRO-CTCAE mobile application for improving patient participation in symptom management during cancer treatment: a randomized controlled trial Lee, Mangyeong Kang, Danbee Kang, Eunjee Kim, Sooyeon Kim, Youngha Ahn, Jin Seok Park, Sehhoon Lee, Yoo-Young Oh, Dongryul Noh, Jae Myung Cho, Juhee Support Care Cancer Research PURPOSE: Although mobile-based symptom monitoring is expected to improve patient participation in symptom management during anticancer therapy, previous trials have not evaluated its effectiveness. Therefore, this study aims to evaluate the impact of a symptom monitoring mobile application on improving patient participation in symptom management during anticancer therapy. METHODS: We conducted a single-center, open-label, randomized controlled trial that enrolled patients with breast, lung, head and neck, esophageal, or gynecologic cancer who were scheduled to receive anticancer therapy (oral or intravenous) between October 2020 and March 2021. We excluded patients with physical or psychological problems. The intervention group received a symptom monitoring application for 8 weeks, and the control group received the usual clinical practice. At 8 weeks, the improvement in patient participation in symptom management was assessed, and additionally quality of life and unplanned clinical visits were assessed. RESULTS: A total of 222 patients were included in the analysis, of whom 142 were randomly assigned to the intervention group and 71 to the control group. The intervention group reported better outcome in patient participation in symptom management than the control group at 8 weeks (mean scores of 8.5 vs. 8.0; P = 0.01). There were no significant differences between the groups in Quality of life (P = 0.88) and unplanned clinical visits (P = 0.39–0.76). CONCLUSIONS: This study is meaningful in figuring out that the mobile-based symptom monitoring made them more engaged in their management. Future research should continue to evaluate the effects of patient participation as mediators of clinical outcomes. TRIAL REGISTRATION: ClinicalTrials.gov NCT04568278. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s00520-023-07779-3. Springer Berlin Heidelberg 2023-05-06 2023 /pmc/articles/PMC10163577/ /pubmed/37148373 http://dx.doi.org/10.1007/s00520-023-07779-3 Text en © The Author(s), under exclusive licence to Springer-Verlag GmbH Germany, part of Springer Nature 2023. Springer Nature or its licensor (e.g. a society or other partner) holds exclusive rights to this article under a publishing agreement with the author(s) or other rightsholder(s); author self-archiving of the accepted manuscript version of this article is solely governed by the terms of such publishing agreement and applicable law. This article is made available via the PMC Open Access Subset for unrestricted research re-use and secondary analysis in any form or by any means with acknowledgement of the original source. These permissions are granted for the duration of the World Health Organization (WHO) declaration of COVID-19 as a global pandemic.
spellingShingle Research
Lee, Mangyeong
Kang, Danbee
Kang, Eunjee
Kim, Sooyeon
Kim, Youngha
Ahn, Jin Seok
Park, Sehhoon
Lee, Yoo-Young
Oh, Dongryul
Noh, Jae Myung
Cho, Juhee
Efficacy of the PRO-CTCAE mobile application for improving patient participation in symptom management during cancer treatment: a randomized controlled trial
title Efficacy of the PRO-CTCAE mobile application for improving patient participation in symptom management during cancer treatment: a randomized controlled trial
title_full Efficacy of the PRO-CTCAE mobile application for improving patient participation in symptom management during cancer treatment: a randomized controlled trial
title_fullStr Efficacy of the PRO-CTCAE mobile application for improving patient participation in symptom management during cancer treatment: a randomized controlled trial
title_full_unstemmed Efficacy of the PRO-CTCAE mobile application for improving patient participation in symptom management during cancer treatment: a randomized controlled trial
title_short Efficacy of the PRO-CTCAE mobile application for improving patient participation in symptom management during cancer treatment: a randomized controlled trial
title_sort efficacy of the pro-ctcae mobile application for improving patient participation in symptom management during cancer treatment: a randomized controlled trial
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10163577/
https://www.ncbi.nlm.nih.gov/pubmed/37148373
http://dx.doi.org/10.1007/s00520-023-07779-3
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