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Protocol of trans-Tasman feasibility randomised controlled trial of the Younger Women’s Wellness After Breast Cancer (YWWACP) lifestyle intervention

BACKGROUND: Younger women (defined as those < 50 years who are likely pre-menopausal at time of diagnosis) with breast cancer often experience persistent treatment-related side effects that adversely affect their physical and psychological wellbeing. The Women’s Wellness After Cancer Program (WWA...

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Autores principales: Sharples, K., Vear, N. K., Porter-Steele, J., Anderson, D. J., Moeke-Maxwell, T. H., Laing, B. B., Young, L., Bailey, T. G., Benge, S., Huang, Y., Crowley, E., Day, R., Cartwright, R., Findlay, M., Porter, D., Kuper, M., Campbell, I., McCarthy, A. L.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9343821/
https://www.ncbi.nlm.nih.gov/pubmed/35918737
http://dx.doi.org/10.1186/s40814-022-01114-z
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author Sharples, K.
Vear, N. K.
Porter-Steele, J.
Anderson, D. J.
Moeke-Maxwell, T. H.
Laing, B. B.
Young, L.
Bailey, T. G.
Benge, S.
Huang, Y.
Crowley, E.
Day, R.
Cartwright, R.
Findlay, M.
Porter, D.
Kuper, M.
Campbell, I.
McCarthy, A. L.
author_facet Sharples, K.
Vear, N. K.
Porter-Steele, J.
Anderson, D. J.
Moeke-Maxwell, T. H.
Laing, B. B.
Young, L.
Bailey, T. G.
Benge, S.
Huang, Y.
Crowley, E.
Day, R.
Cartwright, R.
Findlay, M.
Porter, D.
Kuper, M.
Campbell, I.
McCarthy, A. L.
author_sort Sharples, K.
collection PubMed
description BACKGROUND: Younger women (defined as those < 50 years who are likely pre-menopausal at time of diagnosis) with breast cancer often experience persistent treatment-related side effects that adversely affect their physical and psychological wellbeing. The Women’s Wellness After Cancer Program (WWACP) was adapted and piloted in Australia to address these outcomes in younger women. The aims of this feasibility study are to determine (1) the potential to translate the Younger WWACP (YWWACP) intervention to a broader population base in Aotearoa/New Zealand and Australia, and (2) the potential for success of a larger, international, phase ΙΙΙ, randomised controlled trial. METHODS: This bi-national, randomised, single-blinded controlled trial involves two main study sites in Aotearoa/New Zealand (Kōwhai study) and Australia (EMERALD study). Young women aged 18 to 50 years who completed intensive treatment (surgery, chemotherapy, and/or radiotherapy) for breast cancer in the previous 24 months are eligible. The potential to translate the YWWACP to women in these two populations will be assessed according to several feasibility outcomes. These include examining intervention accessibility, acceptability and uptake; intervention sustainability and adherence; the prevalence components of the intervention in the control group; intervention efficacy; participants’ perception of measurement burden; the effectiveness of planned recruitment strategies; and trial methods and procedures. The studies collectively aim to enrol 60 participants in the intervention group and 60 participants in the control group (total = 120 participants). DISCUSSION: Ethical approval has been received from the Southern Health and Disability Ethics Committee (Kōwhai ref: 19/STH/215), and UnitingCare Human Research Ethics Committee (EMERALD ref: 202103). This study will provide important data on the feasibility of the refined YWWACP in the trans-Tasman context. This study will account for and harmonise cross-country differences to ensure the success of a proposed international grant application for a phase ΙΙΙ randomised controlled trial of this program to improve outcomes in younger women living with breast cancer. TRIAL REGISTRATION: Australian New Zealand Clinical Trials Registry (ANZCTR): Kōwhai ACTRN12620000260921, registered on 27 February 2020. EMERALD ACTRN12621000447853, registered on 19 April 2021. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s40814-022-01114-z.
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spelling pubmed-93438212022-08-02 Protocol of trans-Tasman feasibility randomised controlled trial of the Younger Women’s Wellness After Breast Cancer (YWWACP) lifestyle intervention Sharples, K. Vear, N. K. Porter-Steele, J. Anderson, D. J. Moeke-Maxwell, T. H. Laing, B. B. Young, L. Bailey, T. G. Benge, S. Huang, Y. Crowley, E. Day, R. Cartwright, R. Findlay, M. Porter, D. Kuper, M. Campbell, I. McCarthy, A. L. Pilot Feasibility Stud Study Protocol BACKGROUND: Younger women (defined as those < 50 years who are likely pre-menopausal at time of diagnosis) with breast cancer often experience persistent treatment-related side effects that adversely affect their physical and psychological wellbeing. The Women’s Wellness After Cancer Program (WWACP) was adapted and piloted in Australia to address these outcomes in younger women. The aims of this feasibility study are to determine (1) the potential to translate the Younger WWACP (YWWACP) intervention to a broader population base in Aotearoa/New Zealand and Australia, and (2) the potential for success of a larger, international, phase ΙΙΙ, randomised controlled trial. METHODS: This bi-national, randomised, single-blinded controlled trial involves two main study sites in Aotearoa/New Zealand (Kōwhai study) and Australia (EMERALD study). Young women aged 18 to 50 years who completed intensive treatment (surgery, chemotherapy, and/or radiotherapy) for breast cancer in the previous 24 months are eligible. The potential to translate the YWWACP to women in these two populations will be assessed according to several feasibility outcomes. These include examining intervention accessibility, acceptability and uptake; intervention sustainability and adherence; the prevalence components of the intervention in the control group; intervention efficacy; participants’ perception of measurement burden; the effectiveness of planned recruitment strategies; and trial methods and procedures. The studies collectively aim to enrol 60 participants in the intervention group and 60 participants in the control group (total = 120 participants). DISCUSSION: Ethical approval has been received from the Southern Health and Disability Ethics Committee (Kōwhai ref: 19/STH/215), and UnitingCare Human Research Ethics Committee (EMERALD ref: 202103). This study will provide important data on the feasibility of the refined YWWACP in the trans-Tasman context. This study will account for and harmonise cross-country differences to ensure the success of a proposed international grant application for a phase ΙΙΙ randomised controlled trial of this program to improve outcomes in younger women living with breast cancer. TRIAL REGISTRATION: Australian New Zealand Clinical Trials Registry (ANZCTR): Kōwhai ACTRN12620000260921, registered on 27 February 2020. EMERALD ACTRN12621000447853, registered on 19 April 2021. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s40814-022-01114-z. BioMed Central 2022-08-02 /pmc/articles/PMC9343821/ /pubmed/35918737 http://dx.doi.org/10.1186/s40814-022-01114-z Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Study Protocol
Sharples, K.
Vear, N. K.
Porter-Steele, J.
Anderson, D. J.
Moeke-Maxwell, T. H.
Laing, B. B.
Young, L.
Bailey, T. G.
Benge, S.
Huang, Y.
Crowley, E.
Day, R.
Cartwright, R.
Findlay, M.
Porter, D.
Kuper, M.
Campbell, I.
McCarthy, A. L.
Protocol of trans-Tasman feasibility randomised controlled trial of the Younger Women’s Wellness After Breast Cancer (YWWACP) lifestyle intervention
title Protocol of trans-Tasman feasibility randomised controlled trial of the Younger Women’s Wellness After Breast Cancer (YWWACP) lifestyle intervention
title_full Protocol of trans-Tasman feasibility randomised controlled trial of the Younger Women’s Wellness After Breast Cancer (YWWACP) lifestyle intervention
title_fullStr Protocol of trans-Tasman feasibility randomised controlled trial of the Younger Women’s Wellness After Breast Cancer (YWWACP) lifestyle intervention
title_full_unstemmed Protocol of trans-Tasman feasibility randomised controlled trial of the Younger Women’s Wellness After Breast Cancer (YWWACP) lifestyle intervention
title_short Protocol of trans-Tasman feasibility randomised controlled trial of the Younger Women’s Wellness After Breast Cancer (YWWACP) lifestyle intervention
title_sort protocol of trans-tasman feasibility randomised controlled trial of the younger women’s wellness after breast cancer (ywwacp) lifestyle intervention
topic Study Protocol
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9343821/
https://www.ncbi.nlm.nih.gov/pubmed/35918737
http://dx.doi.org/10.1186/s40814-022-01114-z
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