Cargando…
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...
Autores principales: | , , , , , , , , , , |
---|---|
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 |
_version_ | 1785037912171085824 |
---|---|
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. |
format | Online Article Text |
id | pubmed-10163577 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Springer Berlin Heidelberg |
record_format | MEDLINE/PubMed |
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 |
work_keys_str_mv | AT leemangyeong efficacyoftheproctcaemobileapplicationforimprovingpatientparticipationinsymptommanagementduringcancertreatmentarandomizedcontrolledtrial AT kangdanbee efficacyoftheproctcaemobileapplicationforimprovingpatientparticipationinsymptommanagementduringcancertreatmentarandomizedcontrolledtrial AT kangeunjee efficacyoftheproctcaemobileapplicationforimprovingpatientparticipationinsymptommanagementduringcancertreatmentarandomizedcontrolledtrial AT kimsooyeon efficacyoftheproctcaemobileapplicationforimprovingpatientparticipationinsymptommanagementduringcancertreatmentarandomizedcontrolledtrial AT kimyoungha efficacyoftheproctcaemobileapplicationforimprovingpatientparticipationinsymptommanagementduringcancertreatmentarandomizedcontrolledtrial AT ahnjinseok efficacyoftheproctcaemobileapplicationforimprovingpatientparticipationinsymptommanagementduringcancertreatmentarandomizedcontrolledtrial AT parksehhoon efficacyoftheproctcaemobileapplicationforimprovingpatientparticipationinsymptommanagementduringcancertreatmentarandomizedcontrolledtrial AT leeyooyoung efficacyoftheproctcaemobileapplicationforimprovingpatientparticipationinsymptommanagementduringcancertreatmentarandomizedcontrolledtrial AT ohdongryul efficacyoftheproctcaemobileapplicationforimprovingpatientparticipationinsymptommanagementduringcancertreatmentarandomizedcontrolledtrial AT nohjaemyung efficacyoftheproctcaemobileapplicationforimprovingpatientparticipationinsymptommanagementduringcancertreatmentarandomizedcontrolledtrial AT chojuhee efficacyoftheproctcaemobileapplicationforimprovingpatientparticipationinsymptommanagementduringcancertreatmentarandomizedcontrolledtrial |