Navigating physical activity engagement following a diagnosis of cancer: A qualitative exploration

This qualitative descriptive study explored cancer survivors' experiences of barriers and facilitators to undertaking physical activity to inform how services and professionals might offer better support. Purposive and theoretical sampling was used to recruit 25 people who were up to 5 years po...

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Published inEuropean journal of cancer care Vol. 26; no. 4; pp. e12608 - n/a
Main Authors Cummins, C., Kayes, N.M., Reeve, J., Smith, G., MacLeod, R., McPherson, K.M.
Format Journal Article
LanguageEnglish
Published England Hindawi Limited 01.07.2017
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Abstract This qualitative descriptive study explored cancer survivors' experiences of barriers and facilitators to undertaking physical activity to inform how services and professionals might offer better support. Purposive and theoretical sampling was used to recruit 25 people who were up to 5 years post‐cancer diagnosis. Participants took part in face to face, semi‐structured interviews, and transcripts were analysed using thematic analysis. The analysis identified five interrelated themes which represented cancer survivors' views: 1) You're on your own–a sense of abandonment post‐treatment, and lack of sufficient and tailored information; 2) Dis‐ease–disruption to self and identity, and a heightened awareness of physical self and fragility; 3) Becoming acclimatised–physical activity in the face of treatment‐related side effects and residual impairment; 4) Importance of others–encouragement and support from health professionals, family and friends, and cancer‐specific exercise groups; 5) Meanings people ascribed to physical activity—these were central and could help or hinder engagement. Our findings suggest being able to live well and re‐engage in meaningful activities following a diagnosis of cancer is both complex and challenging. There appear to be gaps in current service provision in supporting the broader health and well‐being of cancer survivors.
AbstractList This qualitative descriptive study explored cancer survivors' experiences of barriers and facilitators to undertaking physical activity to inform how services and professionals might offer better support. Purposive and theoretical sampling was used to recruit 25 people who were up to 5 years post‐cancer diagnosis. Participants took part in face to face, semi‐structured interviews, and transcripts were analysed using thematic analysis. The analysis identified five interrelated themes which represented cancer survivors' views: 1) You're on your own–a sense of abandonment post‐treatment, and lack of sufficient and tailored information; 2) Dis‐ease–disruption to self and identity, and a heightened awareness of physical self and fragility; 3) Becoming acclimatised–physical activity in the face of treatment‐related side effects and residual impairment; 4) Importance of others–encouragement and support from health professionals, family and friends, and cancer‐specific exercise groups; 5) Meanings people ascribed to physical activity—these were central and could help or hinder engagement. Our findings suggest being able to live well and re‐engage in meaningful activities following a diagnosis of cancer is both complex and challenging. There appear to be gaps in current service provision in supporting the broader health and well‐being of cancer survivors.
This qualitative descriptive study explored cancer survivors' experiences of barriers and facilitators to undertaking physical activity to inform how services and professionals might offer better support. Purposive and theoretical sampling was used to recruit 25 people who were up to 5 years post-cancer diagnosis. Participants took part in face to face, semi-structured interviews, and transcripts were analysed using thematic analysis. The analysis identified five interrelated themes which represented cancer survivors' views: 1) You're on your own-a sense of abandonment post-treatment, and lack of sufficient and tailored information; 2) Dis-ease-disruption to self and identity, and a heightened awareness of physical self and fragility; 3) Becoming acclimatised-physical activity in the face of treatment-related side effects and residual impairment; 4) Importance of others-encouragement and support from health professionals, family and friends, and cancer-specific exercise groups; 5) Meanings people ascribed to physical activity--these were central and could help or hinder engagement. Our findings suggest being able to live well and re-engage in meaningful activities following a diagnosis of cancer is both complex and challenging. There appear to be gaps in current service provision in supporting the broader health and well-being of cancer survivors.
Author Cummins, C.
Smith, G.
Kayes, N.M.
Reeve, J.
McPherson, K.M.
MacLeod, R.
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Issue 4
Keywords rehabilitation
cancer
barriers
facilitators
qualitative
physical activity
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Snippet This qualitative descriptive study explored cancer survivors' experiences of barriers and facilitators to undertaking physical activity to inform how services...
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pubmed
wiley
SourceType Aggregation Database
Index Database
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StartPage e12608
SubjectTerms Abandonment
Adaptation, Psychological - classification
Adult
Aged
Aged, 80 and over
barriers
Cancer
Cancer Survivors - psychology
Diagnosis
Disruption
Exercise
Exercise - psychology
facilitators
Female
Fragility
Humans
Interpersonal Relations
Male
Medical diagnosis
Medical personnel
Middle Aged
Motivation
Neoplasms - psychology
Nursing
Patient Navigation - methods
Personal Satisfaction
Physical activity
Physical training
qualitative
rehabilitation
Sampling
Side effects
Social Support
Title Navigating physical activity engagement following a diagnosis of cancer: A qualitative exploration
URI https://onlinelibrary.wiley.com/doi/abs/10.1111%2Fecc.12608
https://www.ncbi.nlm.nih.gov/pubmed/27925326
https://www.proquest.com/docview/1914137179
https://search.proquest.com/docview/1846722726
Volume 26
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