A formative study exploring perceptions of physical activity and physical activity monitoring among children and young people with cystic fibrosis and health care professionals
Open accessAbstract
BACKGROUND: Physical activity (PA) is associated with reduced hospitalisations and maintenance of lung function in patients with Cystic Fibrosis (CF). PA is therefore recommended as part of standard care. Despite this, there is no consensus for monitoring of PA and little is known about perceptions of PA monitoring among children and young people with CF. Therefore, the research aimed to explore patients' perceptions of PA and the acceptability of using PA monitoring devices with children and young people with CF. METHODS: An action research approach was utilised, whereby findings from earlier research phases informed subsequent phases. Four phases were utilised, including patient interviews, PA monitoring, follow-up patient interviews and health care professional (HCP) interviews. Subsequently, an expert panel discussed the study to develop recommendations for practice and future research. RESULTS: Findings suggest that experiences of PA in children and young people with CF are largely comparable to their non-CF peers, with individuals engaging in a variety of activities. CF was not perceived as a barrier per se, although participants acknowledged that they could be limited by their symptoms. Maintenance of health emerged as a key facilitator, in some cases PA offered patients the opportunity to 'normalise' their condition. Participants reported enjoying wearing the monitoring devices and had good compliance. Wrist-worn devices and devices providing feedback were preferred. HCPs recognised the potential benefits of the devices in clinical practice. Recommendations based on these findings are that interventions to promote PA in children and young people with CF should be individualised and involve families to promote PA as part of an active lifestyle. Patients should receive support alongside the PA data obtained from monitoring devices. CONCLUSIONS: PA monitoring devices appear to be an acceptable method for objective assessment of PA among children and young people with CF and their clinicians. Wrist-worn devices, which are unobtrusive and can display feedback, were perceived as most acceptable. By understanding the factors impacting PA, CF health professionals will be better placed to support patients and improve health outcomes.
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Physical activity monitoring devices can contribute to better understanding of the barriers preventing exercise.
“In 2018 Shelley et al. surveyed children/adolescents with CF and their clinicians in the UK and found that physical activity monitoring devices were acceptable to both patients and medical professionals and can contribute to better understanding of the barriers preventing exercise (4).”
From Virtual monitoring in CF – the importance of continuous monitoring in a multi-organ chronic condition (2023) · cites this paper as [4]
The Discussion (Phase 2 and phase 3; page not provided) reports that monitoring devices were acceptable to both patients and clinicians. The Background says clinicians need to understand barriers to physical activity, but the paper does not establish that the devices themselves identify barriers preventing exercise; it describes their potential to provide activity data and inform interventions. (LLM, conf=0.84)
Experimental — accuracy not yet measuredPhysical activity monitoring devices were acceptable to both patients and medical professionals.
“In 2018 Shelley et al. surveyed children/adolescents with CF and their clinicians in the UK and found that physical activity monitoring devices were acceptable to both patients and medical professionals and can contribute to better understanding of the barriers preventing exercise (4).”
From Virtual monitoring in CF – the importance of continuous monitoring in a multi-organ chronic condition (2023) · cites this paper as [4]
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Cites
Webb, A. K. (2006) · Cited by 4,369 · see citing works
How we design feasibility studies
Bowen, D. J., Kreuter, M., Spring, B., Cofta-Woerpel, L., Linnan, L., Weiner, D., Bakken, S., Kaplan, C. P., Squiers, L., Fabrizio, C., et al. (2009) · American Journal of Preventive Medicine · doi:10.1016/j.amepre.2009.02.002 · Cited by 3,922 · see citing works
Age Group Comparability of Raw Accelerometer Output from Wrist- and Hip-Worn Monitors
HILDEBRAND, M., VAN HEES, V. T., HANSEN, B. H., & EKELUND, U. (2014) · Medicine & Science in Sports & Exercise · doi:10.1249/mss.0000000000000289 · Cited by 1,043 · see citing works
van Hees, V. T., Gorzelniak, L., Dean‐Leon, E., Eder, M., Pias, M. R., Taherian, S., Ekelund, U., Renström, F., Franks, P. W., Horsch, A., et al. (2013) · PLoS ONE · doi:10.1371/journal.pone.0061691 · Cited by 937 · see citing works
van Hees, V. T., Fang, Z., Langford, J., Assah, F. K., Mohammad, A., Crochemore‐Silva, I., Trenell, M. I., White, T., Wareham, N. J., & Brage, S. (2014) · Journal of Applied Physiology · doi:10.1152/japplphysiol.00421.2014 · Cited by 680 · see citing works
The Prognostic Value of Exercise Testing in Patients with Cystic Fibrosis
Nixon, P. A., Orenstein, D. M., Kelsey, S. F., & Doershuk, C. F. (1992) · New England Journal of Medicine · doi:10.1056/nejm199212173272504 · Cited by 629 · see citing works
Genotype and Phenotype in Cystic Fibrosis
Zielenski, J. (2000) · Respiration · doi:10.1159/000029497 · Cited by 483 · see citing works
Ferguson, T., Rowlands, A. V., Olds, T., & Maher, C. (2015) · International Journal of Behavioral Nutrition and Physical Activity · doi:10.1186/s12966-015-0201-9 · Cited by 468 · see citing works
The Youth Physical Activity Promotion Model: A Conceptual Bridge Between Theory and Practice
Welk, G. J. (1999) · Quest · doi:10.1080/00336297.1999.10484297 · Cited by 464 · see citing works
Davies, J. C., Alton, E. W. F. W., & Bush, A. (2007) · BMJ · doi:10.1136/bmj.39391.713229.ad · Cited by 306 · see citing works
Wear Compliance and Activity in Children Wearing Wrist- and Hip-Mounted Accelerometers
Fairclough, S. J., Noonan, R. J., Rowlands, A. V., van Hees, V. T., Knowles, Z. R., & Boddy, L. M. (2015) · Medicine & Science in Sports & Exercise · doi:10.1249/mss.0000000000000771 · Cited by 301 · see citing works
Self-citationQuality Control Methods in Accelerometer Data Processing: Defining Minimum Wear Time
Rich, C. S., Geraci, M., Griffiths, L. J., Sera, F., Dezateux, C. A., & Cortina‐Borja, M. (2013) · PLoS ONE · doi:10.1371/journal.pone.0067206 · Cited by 295 · see citing works
Borde, R., Smith, J. J., Sutherland, R., Nathan, N., & Lubans, D. R. (2017) · Obesity Reviews · doi:10.1111/obr.12517 · Cited by 177 · see citing works
Physical activity is independently related to aerobic capacity in cystic fibrosis
Hebestreit, H. U., Kieser, S., Rüdiger, S., Schenk, T., Junge, S., Hebestreit, A., Ballmann, M., Posselt, H., & Kriemler, S. (2006) · European Respiratory Journal · doi:10.1183/09031936.06.00128605 · Cited by 141 · see citing works
Longitudinal relationship between physical activity and lung health in patients with cystic fibrosis
Schneiderman, J. E., Wilkes, D. L., Atenafu, E. G., Nguyen, T., Wells, G. D., Alarie, N., Tullis, E. D., Lands, L. C., Coates, A. L., Corey, M. L., et al. (2013) · European Respiratory Journal · doi:10.1183/09031936.00055513 · Cited by 135 · see citing works
Fereday, J. A., MacDougall, C., Spizzo, M., Darbyshire, P., & Schiller, W. (2009) · BMC Pediatrics · doi:10.1186/1471-2431-9-1 · Cited by 113 · see citing works
Effects of Exercise on Respiratory Flow and Sputum Properties in Patients With Cystic Fibrosis
Dwyer, T., Alison, J. A., McKeough, Z. J., Daviskas, E., & Bye, P. T. P. (2010) · CHEST Journal · doi:10.1378/chest.10-1158 · Cited by 105 · see citing works
Factors that influence adherence to exercise and their effectiveness: Application to cystic fibrosis
Prasad, S. A., & Cerny, F. (2002) · Pediatric Pulmonology · doi:10.1002/ppul.10126 · Cited by 102 · see citing works
Comment on “Estimating Activity and Sedentary Behavior from an Accelerometer on the Hip and Wrist”
Freedson, P. S., & John, D. (2013) · Medicine & Science in Sports & Exercise · doi:10.1249/mss.0b013e31827f024d · Cited by 90 · see citing works
A survey of exercise testing and training in UK cystic fibrosis clinics
Stevens, D. J., OADES, P. J., Armstrong, N., et al. (2010) · Journal of Cystic Fibrosis · doi:10.1016/j.jcf.2010.03.004 · Cited by 77 · see citing works
Bone Health, Daily Physical Activity, and Exercise Tolerance in Patients With Cystic Fibrosis
Tejero, S., Sánchez, M. Á. G., Cejudo, P., Quintana‐Gallego, E., Dapena, J., Jiménez, R. G., Luis, P. C., & de Terreros, I. G. (2011) · CHEST Journal · doi:10.1378/chest.10-1508 · Cited by 71 · see citing works
Physical activity participation by adults with cystic fibrosis: An observational study
Cox, N. S., Alison, J. A., Button, B., Wilson, J. W., Morton, J. M., & Holland, A. E. (2015) · Respirology · doi:10.1111/resp.12719 · Cited by 56 · see citing works
Combined Exercise Training Improves Glycemic Control in Adult with Cystic Fibrosis
Beaudoin, N., Bouvet, G. F., Coriati, A., et al. (2016) · Medicine & Science in Sports & Exercise · doi:10.1249/mss.0000000000001104 · Cited by 56 · see citing works
The evolution of exercise capacity and its limiting factors in Cystic Fibrosis
Almajed, A., & Lands, L. C. (2012) · Paediatric Respiratory Reviews · doi:10.1016/j.prrv.2012.01.001 · Cited by 49 · see citing works
"No Time to Play": Perceptions Toward Physical Activity in Youth With Cystic Fibrosis
Moola, F. J., Faulkner, G., & Schneiderman, J. E. (2012) · Adapted Physical Activity Quarterly · doi:10.1123/apaq.29.1.44 · Cited by 48 · see citing works
Verloigne, M., Bere, E. T., Lippevelde, W. V., Maes, L., Lien, N., Vik, F. N., Brug, J., Cardon, G., & Bourdeaudhuij, I. D. (2012) · BMC Public Health · doi:10.1186/1471-2458-12-805 · Cited by 46 · see citing works
First Dinosaurs from Saudi Arabia
Kear, B. P., Rich, T. H., Vickers-Rich, P., et al. (2013) · PLoS ONE · doi:10.1371/journal.pone.0084041 · Cited by 45 · see citing works
Physical activity assessment in cystic fibrosis: A position statement
Bradley, J. M., O'Neill, B. M., Kent, L., et al. (2015) · Journal of Cystic Fibrosis · doi:10.1016/j.jcf.2015.05.011 · Cited by 44 · see citing works
Exercise and Habitual Physical Activity for People With Cystic Fibrosis
Swisher, A. K., Hebestreit, H. U., Mejia-Downs, A., Lowman, J. D., Gruber, W., Nippins, M., Alison, J. A., & Schneiderman, J. E. (2015) · Cardiopulmonary Physical Therapy Journal · doi:10.1097/cpt.0000000000000016 · Cited by 44 · see citing works
Quality Control Methods in Accelerometer Data Processing: Identifying Extreme Counts
Rich, C. S., Geraci, M., Griffiths, L. J., Sera, F., Dezateux, C. A., & Cortina‐Borja, M. (2014) · PLoS ONE · doi:10.1371/journal.pone.0085134 · Cited by 36 · see citing works
Jantzen, A., Opoku‐Pare, M., Bieli, C., et al. (2016) · Pediatric Pulmonology · doi:10.1002/ppul.23532 · Cited by 21 · see citing works
Motion sensors for monitoring physical activity in cystic fibrosis: what is the next step?
Bradley, J. M., Kent, L., Elborn, J. S., & O'Neill, B. M. (2010) · Physical Therapy Reviews · doi:10.1179/1743288x10y.0000000005 · Cited by 13 · see citing works
Moola, F. J., Faulkner, G., & Schneiderman, J. E. (2011) · Open Journal of Preventive Medicine · doi:10.4236/ojpm.2011.13016 · Cited by 12 · see citing works
Experiences of physical activity: A phenomenological study of individuals with cystic fibrosis
Street, R., Mercer, J., Mills-Bennett, R., et al. (2014) · Journal of Health Psychology · doi:10.1177/1359105314527141 · Cited by 8 · see citing works
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Curran, M., Tierney, A. C., Collins, L., Kennedy, L., McDonnell, C., Jurascheck, A. J., Sheikhi, A., Walsh, C., Button, B., Casserly, B., et al. (2023) · Journal of Cystic Fibrosis · doi:10.1016/j.jcf.2022.11.002 · Cited by 15 · see citing works
Vagg, T., Deasy, K. F., Chapman, W. W., Ranganathan, S. C., Plant, B. J., & Shanthikumar, S. (2023) · Frontiers in Digital Health · doi:10.3389/fdgth.2023.1196442 · Cited by 1 · see citing works
“surveyed children/ adolescents with CF and their clinicians in the UK and found that physical activity monitoring devices were acceptable to both patients and medical professionals and can contribute to better understanding of the barriers preventing exercise (4).”
Background
- Authors
- Shelley, J., Fairclough, S. J., Knowles, Z. R., Southern, K. W., McCormack, P., Dawson, E. A., Graves, L. E. F., & Hanlon, C.
- Affiliations
- Liverpool John Moores University (GB)
- Edge Hill University (GB)
- University of Liverpool (GB)
- Alder Hey Children's NHS Foundation Trust (GB)
- Corresponding author
- Shelley, James
- ORCID
- Venue
- BMC Pediatrics
- Published
- 2018-10-23
- Volume
- 18
- Issue
- 1
- Pages
- 335-335
- ISSN
- 1471-2431 (ISSN-L)
- PMC
- PMC6198445
- OpenAlex
- W2897789466
- Cited by
- 31
- References
- 34
- Citations by year
- 2026: 1 · 2025: 2 · 2024: 4 · 2023: 3 · 2022: 14 · 2021: 3 · 2020: 4
- FWCI
- 1.20
- Type
- journal article
- Language
- en
- Open access
- gold
- doi.org
- Licence
- Locations
- BMC Pediatrics (publishedVersion, cc-by)
- Europe PMC (PubMed Central) (publishedVersion, other-oa)
- PubMed Central (publishedVersion, cc-by)
- PubMed (publishedVersion)
- Liverpool John Moores University (acceptedVersion)
- DOAJ (DOAJ: Directory of Open Access Journals) (submittedVersion, cc-by-sa)
- Lancaster EPrints (Lancaster University) (submittedVersion)
- Edge Hill University Research Information Repository (Edge Hill University) (submittedVersion, cc-by)
- Funders
- Bupa Foundation
- Topics
- Health Sciences › Medicine › Physiology › Physical Activity and Health
- Health Sciences › Medicine › Pulmonary and Respiratory Medicine › Cystic Fibrosis Research Advances
- Health Sciences › Health Professions › General Health Professions › Mobile Health and mHealth Applications
- Keywords
- cystic fibrosis, physical activity, physical activity monitoring, wearable activity trackers, children and young people, patient perspectives, healthcare workers, acceptability, wrist-worn devices, feedback devices, family involvement, individualised intervention, lung function
- MeSH terms
- Fitness Trackers, Attitude of Health Personnel, Attitude to Health, Cystic Fibrosis, Humans, Interviews as Topic, Patient Compliance, Perception, Exercise
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