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Physical activity in adults with Cystic Fibrosis.

Longitudinal assessment of physical activity in adults with Cystic Fibrosis.

Status
Completed
Phases
Unknown
Study type
Observational
Source
ANZCTR
Registry ID
ACTRN12610000949088
Enrollment
65
Registered
2010-11-05
Start date
2011-02-03
Completion date
2012-09-06
Last updated
2020-01-13

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

None listed

Brief summary

Regular physical activity has many health benefits. More specifically, physical inactivity is an identified risk factor for global mortality, and can contribute to the incidence of non-communicable diseases such as obesity and heart disease. In generally healthy adults at least 150 minutes of moderate-vigorous intensity physical activity each week is required to improve cardiorespiratory fitness, bone health and reduce the risk of non-communicable diseases and depression. In individuals with CF there are no established targets for physical activity participation. Consequently, physical activity interventions are shaped around guidelines for healthy adults. Improving and maintaining physical activity is a cornerstone of therapy for CF patients. Aerobic fitness is associated with improved survival and those with better physical fitness have better quality of life. Despite this, participation in exercise decreases with increasing perception of disease severity, with patients ascribing decreased importance and increased burden to exercise over other therapies. In previous studies of physical activity in CF, both children and adults have been found to undertake less moderate-vigorous physical activity than their healthy peers. It is hypothesised that: 1. Physical activity decreases over time in CF and is more marked in particular sub-groups such as females and those with repeated need for intravenous (IV) antibiotics. 2. Factors such as higher baseline respiratory function, fulltime employment/study, higher fitness levels, younger age and male gender will all be associated with better long-term participation in physical activity. 3. Physical activity is decreased after respiratory exacerbation requiring IV antibiotics, and does not return to baseline after 4 weeks. 4. Decline in physical activity is associated with a more rapid decline in respiratory function over 12 months.

Interventions

This study will assess habitual physical activity participation in adults with Cystic Fibrosis over a 12 month period. Physical activity will be assessed using a bi-axial accelerometer (Sensewear Armband [Bodymedia]). Participants will be assessed at baseline and 12 months. Measures of respiratory function, quality of life, intention to exercise and exercise capacity will be performed prior to the wearing of the activity monitor for a period of 5 to 7 days. By measuring physical activity in

This study will assess habitual physical activity participation in adults with Cystic Fibrosis over a 12 month period. Physical activity will be assessed using a bi-axial accelerometer (Sensewear Armband [Bodymedia]). Participants will be assessed at baseline and 12 months. Measures of respiratory function, quality of life, intention to exercise and exercise capacity will be performed prior to the wearing of the activity monitor for a period of 5 to 7 days. By measuring physical activity in this way we will be able to objectively quantify physical activity participation in adults with CF over a prolonged period. Additionally, we hope to identify the presence of clinical or demographic characteristics which determine long-term participation in physical activity; To examine the effect of a respiratory exacerbation requiring IV antibiotics on physical activity participation, as compared to baseline, in adults with CF; and, to ascertain what relationship exists between change in respiratory function and change in physical activity participation over time.

Sponsors

Narelle Cox
Lead SponsorIndividual

Eligibility

Sex/Gender
All
Age
18 Years to 60 Years
Healthy volunteers
No

Inclusion criteria

Diagnosis of Cystic Fibrosis Age greater than 18 years Able to provide informed consent

Exclusion criteria

Presence of severe co-morbidity limiting mobilisation or physical activity participation (eg. orthopaedic, cardiac or neurological condition). Colonization with Burkholderia cepacia. Adults with Cystic Fibrosis who have had or are actively awaiting lung transplantation. Respiratory exacerbation requiring intravenous antibiotics in the previous 6 weeks.

Outcome results

None listed

Source: ANZCTR · Data processed: Feb 4, 2026