Effect of progressive resistance training on health-related quality of life in the first year after breast cancer surgery - results from a randomized controlled trial

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Standard

Effect of progressive resistance training on health-related quality of life in the first year after breast cancer surgery - results from a randomized controlled trial. / Ammitzbøll, Gunn; Kristina Kjær, Trille; Johansen, Christoffer; Lanng, Charlotte; Wreford Andersen, Elisabeth; Kroman, Niels; Zerahn, Bo; Hyldegaard, Ole; Envold Bidstrup, Pernille; Oksbjerg Dalton, Susanne.

I: Acta Oncologica, Bind 58, Nr. 5, 05.2019, s. 665-672.

Publikation: Bidrag til tidsskriftTidsskriftartikelForskningfagfællebedømt

Harvard

Ammitzbøll, G, Kristina Kjær, T, Johansen, C, Lanng, C, Wreford Andersen, E, Kroman, N, Zerahn, B, Hyldegaard, O, Envold Bidstrup, P & Oksbjerg Dalton, S 2019, 'Effect of progressive resistance training on health-related quality of life in the first year after breast cancer surgery - results from a randomized controlled trial', Acta Oncologica, bind 58, nr. 5, s. 665-672. https://doi.org/10.1080/0284186X.2018.1563718

APA

Ammitzbøll, G., Kristina Kjær, T., Johansen, C., Lanng, C., Wreford Andersen, E., Kroman, N., Zerahn, B., Hyldegaard, O., Envold Bidstrup, P., & Oksbjerg Dalton, S. (2019). Effect of progressive resistance training on health-related quality of life in the first year after breast cancer surgery - results from a randomized controlled trial. Acta Oncologica, 58(5), 665-672. https://doi.org/10.1080/0284186X.2018.1563718

Vancouver

Ammitzbøll G, Kristina Kjær T, Johansen C, Lanng C, Wreford Andersen E, Kroman N o.a. Effect of progressive resistance training on health-related quality of life in the first year after breast cancer surgery - results from a randomized controlled trial. Acta Oncologica. 2019 maj;58(5):665-672. https://doi.org/10.1080/0284186X.2018.1563718

Author

Ammitzbøll, Gunn ; Kristina Kjær, Trille ; Johansen, Christoffer ; Lanng, Charlotte ; Wreford Andersen, Elisabeth ; Kroman, Niels ; Zerahn, Bo ; Hyldegaard, Ole ; Envold Bidstrup, Pernille ; Oksbjerg Dalton, Susanne. / Effect of progressive resistance training on health-related quality of life in the first year after breast cancer surgery - results from a randomized controlled trial. I: Acta Oncologica. 2019 ; Bind 58, Nr. 5. s. 665-672.

Bibtex

@article{28a68268c2414deb8e92d38e0bb0c04d,
title = "Effect of progressive resistance training on health-related quality of life in the first year after breast cancer surgery - results from a randomized controlled trial",
abstract = "Aims: To examine the effect of progressive resistance training (PRT) on health related quality of life and a predefined symptom cluster of pain-sleep-fatigue. Methods: This study was a planned secondary analysis of a randomized controlled trial examining the effect of PRT on prevention of arm lymphedema in a population of women between 18 and 75 years undergoing breast cancer surgery with axillary lymph node dissection. Participants were allocated by computer randomization to usual care control or a PRT intervention in a 1:1 ratio. The intervention, initiated in the third post-operative week, consisted of three times PRT per week, supervised in groups in the first 20 weeks, and self-administered in the following 30 weeks. Questionnaire assessments were made at baseline, 20 weeks and 12 months, with the European Organization for Research and Treatment in Cancer Core questionnaire (EORTC QLQ C30) and the Functional Assessment of Chronic Illness Therapy-(FACIT) fatigue questionnaire. The symptom cluster of pain-sleep-fatigue was measured with a constructed score adding EORTC C30 subscales of insomnia, pain, and fatigue. Data were treated as repeated measurements and analyzed with mixed models. Results: Among 158 recruited participants, we found a clinically relevant increased emotional functioning with nine points at both follow-ups (p = .02), and 16 and 11 points at 20 weeks and 12 months respectively (p = .04) in social functioning. Furthermore, in the subgroup of women with the symptom cluster pain-sleep-fatigue present at baseline, a significant effect was found for global health status (p = .01) and social functioning (p = .02). Conclusion: To our knowledge, this is the first study to report clinically relevant effects of PRT on social and emotional functioning in the first postoperative year after breast cancer surgery. Furthermore, a subgroup of women with the pain-sleep-fatigue symptom cluster had particular benefit from PRT on global health status and social functioning.",
keywords = "Adult, Aged, Breast Neoplasms/surgery, Fatigue/etiology, Female, Humans, Lymphedema/prevention & control, Mastectomy/adverse effects, Middle Aged, Postoperative Complications/etiology, Quality of Life, Resistance Training, Treatment Outcome",
author = "Gunn Ammitzb{\o}ll and {Kristina Kj{\ae}r}, Trille and Christoffer Johansen and Charlotte Lanng and {Wreford Andersen}, Elisabeth and Niels Kroman and Bo Zerahn and Ole Hyldegaard and {Envold Bidstrup}, Pernille and {Oksbjerg Dalton}, Susanne",
year = "2019",
month = may,
doi = "10.1080/0284186X.2018.1563718",
language = "English",
volume = "58",
pages = "665--672",
journal = "Acta Oncologica",
issn = "1100-1704",
publisher = "Taylor & Francis",
number = "5",

}

RIS

TY - JOUR

T1 - Effect of progressive resistance training on health-related quality of life in the first year after breast cancer surgery - results from a randomized controlled trial

AU - Ammitzbøll, Gunn

AU - Kristina Kjær, Trille

AU - Johansen, Christoffer

AU - Lanng, Charlotte

AU - Wreford Andersen, Elisabeth

AU - Kroman, Niels

AU - Zerahn, Bo

AU - Hyldegaard, Ole

AU - Envold Bidstrup, Pernille

AU - Oksbjerg Dalton, Susanne

PY - 2019/5

Y1 - 2019/5

N2 - Aims: To examine the effect of progressive resistance training (PRT) on health related quality of life and a predefined symptom cluster of pain-sleep-fatigue. Methods: This study was a planned secondary analysis of a randomized controlled trial examining the effect of PRT on prevention of arm lymphedema in a population of women between 18 and 75 years undergoing breast cancer surgery with axillary lymph node dissection. Participants were allocated by computer randomization to usual care control or a PRT intervention in a 1:1 ratio. The intervention, initiated in the third post-operative week, consisted of three times PRT per week, supervised in groups in the first 20 weeks, and self-administered in the following 30 weeks. Questionnaire assessments were made at baseline, 20 weeks and 12 months, with the European Organization for Research and Treatment in Cancer Core questionnaire (EORTC QLQ C30) and the Functional Assessment of Chronic Illness Therapy-(FACIT) fatigue questionnaire. The symptom cluster of pain-sleep-fatigue was measured with a constructed score adding EORTC C30 subscales of insomnia, pain, and fatigue. Data were treated as repeated measurements and analyzed with mixed models. Results: Among 158 recruited participants, we found a clinically relevant increased emotional functioning with nine points at both follow-ups (p = .02), and 16 and 11 points at 20 weeks and 12 months respectively (p = .04) in social functioning. Furthermore, in the subgroup of women with the symptom cluster pain-sleep-fatigue present at baseline, a significant effect was found for global health status (p = .01) and social functioning (p = .02). Conclusion: To our knowledge, this is the first study to report clinically relevant effects of PRT on social and emotional functioning in the first postoperative year after breast cancer surgery. Furthermore, a subgroup of women with the pain-sleep-fatigue symptom cluster had particular benefit from PRT on global health status and social functioning.

AB - Aims: To examine the effect of progressive resistance training (PRT) on health related quality of life and a predefined symptom cluster of pain-sleep-fatigue. Methods: This study was a planned secondary analysis of a randomized controlled trial examining the effect of PRT on prevention of arm lymphedema in a population of women between 18 and 75 years undergoing breast cancer surgery with axillary lymph node dissection. Participants were allocated by computer randomization to usual care control or a PRT intervention in a 1:1 ratio. The intervention, initiated in the third post-operative week, consisted of three times PRT per week, supervised in groups in the first 20 weeks, and self-administered in the following 30 weeks. Questionnaire assessments were made at baseline, 20 weeks and 12 months, with the European Organization for Research and Treatment in Cancer Core questionnaire (EORTC QLQ C30) and the Functional Assessment of Chronic Illness Therapy-(FACIT) fatigue questionnaire. The symptom cluster of pain-sleep-fatigue was measured with a constructed score adding EORTC C30 subscales of insomnia, pain, and fatigue. Data were treated as repeated measurements and analyzed with mixed models. Results: Among 158 recruited participants, we found a clinically relevant increased emotional functioning with nine points at both follow-ups (p = .02), and 16 and 11 points at 20 weeks and 12 months respectively (p = .04) in social functioning. Furthermore, in the subgroup of women with the symptom cluster pain-sleep-fatigue present at baseline, a significant effect was found for global health status (p = .01) and social functioning (p = .02). Conclusion: To our knowledge, this is the first study to report clinically relevant effects of PRT on social and emotional functioning in the first postoperative year after breast cancer surgery. Furthermore, a subgroup of women with the pain-sleep-fatigue symptom cluster had particular benefit from PRT on global health status and social functioning.

KW - Adult

KW - Aged

KW - Breast Neoplasms/surgery

KW - Fatigue/etiology

KW - Female

KW - Humans

KW - Lymphedema/prevention & control

KW - Mastectomy/adverse effects

KW - Middle Aged

KW - Postoperative Complications/etiology

KW - Quality of Life

KW - Resistance Training

KW - Treatment Outcome

U2 - 10.1080/0284186X.2018.1563718

DO - 10.1080/0284186X.2018.1563718

M3 - Journal article

C2 - 30702006

VL - 58

SP - 665

EP - 672

JO - Acta Oncologica

JF - Acta Oncologica

SN - 1100-1704

IS - 5

ER -

ID: 232910205