Exercise volume load in women with breast cancer: study protocol for the ABRACE randomized clinical trial
Autor(a) principal: | |
---|---|
Data de Publicação: | 2023 |
Outros Autores: | , , , , |
Tipo de documento: | Artigo |
Idioma: | eng |
Título da fonte: | Repositório Institucional da UFRGS |
Texto Completo: | http://hdl.handle.net/10183/265185 |
Resumo: | Background: An increased number of breast cancer patients are challenged by acute and persistent treatment side effects. Oncology guidelines have been establishing physical exercise to counteract several treatment-related toxicities throughout cancer care. However, evidence regarding the optimal dose-response, feasibility, and the minimal resistance exercise volume and/or intensity remains unclear. The ABRACE Study will assess the impact of different resistance training volumes (i.e., single or multiple sets) combined with aerobic exercise on physical and psychological outcomes of breast cancer patients undergoing primary treatment. Methods: This study is a randomized, controlled, three-armed parallel trial. A total of 84 participants, aged ≥18 years, with breast cancer stages I-III, initiating adjuvant or neoadjuvant chemotherapy (≤50% of sessions completed) will be randomized to multiple sets resistance training plus aerobic training group, single set resistance training plus aerobic training group or control group. Neuromuscular and cancer-related fatigue (primary outcomes), muscle strength, muscle thickness, muscle quality by echo intensity, body composition, cardiorespiratory capacity, functional performance, upper-body endurance and quality of life will be measured before and after the 12-week intervention. Our analysis will follow the intention-to-treat approach and per-protocol criteria, with additional sub-group analysis. Discussion: Findings support prescribing exercise during chemotherapy for breast cancer and elucidate the potential role of different resistance training volumes as a management strategy for physical and psychological impairments in women with early-stage breast cancer. Our main hypothesis is for superiority in physical and psychological outcomes for both training groups compared to the control group, with no difference between single or multiple sets groups. |
id |
UFRGS-2_72860b40be5c1ab2054ed1149492bae9 |
---|---|
oai_identifier_str |
oai:www.lume.ufrgs.br:10183/265185 |
network_acronym_str |
UFRGS-2 |
network_name_str |
Repositório Institucional da UFRGS |
repository_id_str |
|
spelling |
Henkin, João SaldanhaRosa, Daniela DornellesMorelle, Alessandra MenezesCaleffi, MairaPinto, Stephanie SantanaPinto, Ronei Silveira2023-09-26T03:34:50Z20232451-8654http://hdl.handle.net/10183/265185001169856Background: An increased number of breast cancer patients are challenged by acute and persistent treatment side effects. Oncology guidelines have been establishing physical exercise to counteract several treatment-related toxicities throughout cancer care. However, evidence regarding the optimal dose-response, feasibility, and the minimal resistance exercise volume and/or intensity remains unclear. The ABRACE Study will assess the impact of different resistance training volumes (i.e., single or multiple sets) combined with aerobic exercise on physical and psychological outcomes of breast cancer patients undergoing primary treatment. Methods: This study is a randomized, controlled, three-armed parallel trial. A total of 84 participants, aged ≥18 years, with breast cancer stages I-III, initiating adjuvant or neoadjuvant chemotherapy (≤50% of sessions completed) will be randomized to multiple sets resistance training plus aerobic training group, single set resistance training plus aerobic training group or control group. Neuromuscular and cancer-related fatigue (primary outcomes), muscle strength, muscle thickness, muscle quality by echo intensity, body composition, cardiorespiratory capacity, functional performance, upper-body endurance and quality of life will be measured before and after the 12-week intervention. Our analysis will follow the intention-to-treat approach and per-protocol criteria, with additional sub-group analysis. Discussion: Findings support prescribing exercise during chemotherapy for breast cancer and elucidate the potential role of different resistance training volumes as a management strategy for physical and psychological impairments in women with early-stage breast cancer. Our main hypothesis is for superiority in physical and psychological outcomes for both training groups compared to the control group, with no difference between single or multiple sets groups.application/pdfengContemporary clinical trials communications. [Amsterdam]. Vol. 31 (Feb. 2023), artigo 101053, 8 p.Neoplasias da mamaFadiga físicaExercício físicoTreinamento de forçaBreast neoplasmsCombined trainingFatiguePhysical exerciseStrength trainingExercise volume load in women with breast cancer: study protocol for the ABRACE randomized clinical trialEstrangeiroinfo:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/openAccessreponame:Repositório Institucional da UFRGSinstname:Universidade Federal do Rio Grande do Sul (UFRGS)instacron:UFRGSTEXT001169856.pdf.txt001169856.pdf.txtExtracted Texttext/plain52397http://www.lume.ufrgs.br/bitstream/10183/265185/2/001169856.pdf.txtd3eacf945c7d64e1e21188264857b6f2MD52ORIGINAL001169856.pdfTexto completo (inglês)application/pdf989734http://www.lume.ufrgs.br/bitstream/10183/265185/1/001169856.pdf449674dcd5266bfa3b5f7a0161636187MD5110183/2651852023-09-27 03:34:41.081536oai:www.lume.ufrgs.br:10183/265185Repositório de PublicaçõesPUBhttps://lume.ufrgs.br/oai/requestopendoar:2023-09-27T06:34:41Repositório Institucional da UFRGS - Universidade Federal do Rio Grande do Sul (UFRGS)false |
dc.title.pt_BR.fl_str_mv |
Exercise volume load in women with breast cancer: study protocol for the ABRACE randomized clinical trial |
title |
Exercise volume load in women with breast cancer: study protocol for the ABRACE randomized clinical trial |
spellingShingle |
Exercise volume load in women with breast cancer: study protocol for the ABRACE randomized clinical trial Henkin, João Saldanha Neoplasias da mama Fadiga física Exercício físico Treinamento de força Breast neoplasms Combined training Fatigue Physical exercise Strength training |
title_short |
Exercise volume load in women with breast cancer: study protocol for the ABRACE randomized clinical trial |
title_full |
Exercise volume load in women with breast cancer: study protocol for the ABRACE randomized clinical trial |
title_fullStr |
Exercise volume load in women with breast cancer: study protocol for the ABRACE randomized clinical trial |
title_full_unstemmed |
Exercise volume load in women with breast cancer: study protocol for the ABRACE randomized clinical trial |
title_sort |
Exercise volume load in women with breast cancer: study protocol for the ABRACE randomized clinical trial |
author |
Henkin, João Saldanha |
author_facet |
Henkin, João Saldanha Rosa, Daniela Dornelles Morelle, Alessandra Menezes Caleffi, Maira Pinto, Stephanie Santana Pinto, Ronei Silveira |
author_role |
author |
author2 |
Rosa, Daniela Dornelles Morelle, Alessandra Menezes Caleffi, Maira Pinto, Stephanie Santana Pinto, Ronei Silveira |
author2_role |
author author author author author |
dc.contributor.author.fl_str_mv |
Henkin, João Saldanha Rosa, Daniela Dornelles Morelle, Alessandra Menezes Caleffi, Maira Pinto, Stephanie Santana Pinto, Ronei Silveira |
dc.subject.por.fl_str_mv |
Neoplasias da mama Fadiga física Exercício físico Treinamento de força |
topic |
Neoplasias da mama Fadiga física Exercício físico Treinamento de força Breast neoplasms Combined training Fatigue Physical exercise Strength training |
dc.subject.eng.fl_str_mv |
Breast neoplasms Combined training Fatigue Physical exercise Strength training |
description |
Background: An increased number of breast cancer patients are challenged by acute and persistent treatment side effects. Oncology guidelines have been establishing physical exercise to counteract several treatment-related toxicities throughout cancer care. However, evidence regarding the optimal dose-response, feasibility, and the minimal resistance exercise volume and/or intensity remains unclear. The ABRACE Study will assess the impact of different resistance training volumes (i.e., single or multiple sets) combined with aerobic exercise on physical and psychological outcomes of breast cancer patients undergoing primary treatment. Methods: This study is a randomized, controlled, three-armed parallel trial. A total of 84 participants, aged ≥18 years, with breast cancer stages I-III, initiating adjuvant or neoadjuvant chemotherapy (≤50% of sessions completed) will be randomized to multiple sets resistance training plus aerobic training group, single set resistance training plus aerobic training group or control group. Neuromuscular and cancer-related fatigue (primary outcomes), muscle strength, muscle thickness, muscle quality by echo intensity, body composition, cardiorespiratory capacity, functional performance, upper-body endurance and quality of life will be measured before and after the 12-week intervention. Our analysis will follow the intention-to-treat approach and per-protocol criteria, with additional sub-group analysis. Discussion: Findings support prescribing exercise during chemotherapy for breast cancer and elucidate the potential role of different resistance training volumes as a management strategy for physical and psychological impairments in women with early-stage breast cancer. Our main hypothesis is for superiority in physical and psychological outcomes for both training groups compared to the control group, with no difference between single or multiple sets groups. |
publishDate |
2023 |
dc.date.accessioned.fl_str_mv |
2023-09-26T03:34:50Z |
dc.date.issued.fl_str_mv |
2023 |
dc.type.driver.fl_str_mv |
Estrangeiro info:eu-repo/semantics/article |
dc.type.status.fl_str_mv |
info:eu-repo/semantics/publishedVersion |
format |
article |
status_str |
publishedVersion |
dc.identifier.uri.fl_str_mv |
http://hdl.handle.net/10183/265185 |
dc.identifier.issn.pt_BR.fl_str_mv |
2451-8654 |
dc.identifier.nrb.pt_BR.fl_str_mv |
001169856 |
identifier_str_mv |
2451-8654 001169856 |
url |
http://hdl.handle.net/10183/265185 |
dc.language.iso.fl_str_mv |
eng |
language |
eng |
dc.relation.ispartof.pt_BR.fl_str_mv |
Contemporary clinical trials communications. [Amsterdam]. Vol. 31 (Feb. 2023), artigo 101053, 8 p. |
dc.rights.driver.fl_str_mv |
info:eu-repo/semantics/openAccess |
eu_rights_str_mv |
openAccess |
dc.format.none.fl_str_mv |
application/pdf |
dc.source.none.fl_str_mv |
reponame:Repositório Institucional da UFRGS instname:Universidade Federal do Rio Grande do Sul (UFRGS) instacron:UFRGS |
instname_str |
Universidade Federal do Rio Grande do Sul (UFRGS) |
instacron_str |
UFRGS |
institution |
UFRGS |
reponame_str |
Repositório Institucional da UFRGS |
collection |
Repositório Institucional da UFRGS |
bitstream.url.fl_str_mv |
http://www.lume.ufrgs.br/bitstream/10183/265185/2/001169856.pdf.txt http://www.lume.ufrgs.br/bitstream/10183/265185/1/001169856.pdf |
bitstream.checksum.fl_str_mv |
d3eacf945c7d64e1e21188264857b6f2 449674dcd5266bfa3b5f7a0161636187 |
bitstream.checksumAlgorithm.fl_str_mv |
MD5 MD5 |
repository.name.fl_str_mv |
Repositório Institucional da UFRGS - Universidade Federal do Rio Grande do Sul (UFRGS) |
repository.mail.fl_str_mv |
|
_version_ |
1815447839498567680 |