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Effect of an exercise program on function, activity and participation of young people with cystic fibrosis

Effect of a targeted exercise program versus current exercise practice on function, activity and participation of young people with cystic fibrosis: a randomised controlled trial

Status
Completed
Phases
Unknown
Study type
Interventional
Source
ANZCTR
Registry ID
ACTRN12607000612415
Enrollment
32
Registered
2007-11-28
Start date
2007-04-02
Completion date
2008-01-31
Last updated
2021-06-14

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

Conditions

None listed

Brief summary

Exercise is a vital component of the physiotherapy management for young people with cystic fibrosis (CF). The overall aim of this research is to strengthen knowledge about best practice exercise programs for this population. This study compares effects of two exercise programs (the current exercise practice versus a novel targeted exercise program). Ultimately, it is expected that with improved exercise programs, young people with CF may have improved body structure and function, and activity and participation levels, leading to enhanced quality of life.

Interventions

Participants allocated to the intervention group receive usual inpatient treatment, including medical, nutritional and physiotherapy. In place of the usual physiotherapy exercise program, participants in this group receive a targeted exercise program, addressing components of strength, flexibility and aerobic and anaerobic activities. This supervised program is performed five days per week (for up to 60 minutes), and is encouraged to be continued over the weekend (supervised by parent / guardian

Participants allocated to the intervention group receive usual inpatient treatment, including medical, nutritional and physiotherapy. In place of the usual physiotherapy exercise program, participants in this group receive a targeted exercise program, addressing components of strength, flexibility and aerobic and anaerobic activities. This supervised program is performed five days per week (for up to 60 minutes), and is encouraged to be continued over the weekend (supervised by parent / guardian). Participants receive an exercise pack which includes items to encourage physical activity. A log is used for documentation of activities and relevant measures (for example: heart rate, breathlessness score, shuttle level attained or number of jumps performed in 30 seconds etc). A pedometer is provided to count the number of steps taken during the session and between sessions. Prior to discharge from hospital, advice is given regarding continuation of the program at home, aiming for 30 minutes on three days per week. This program is continued for 12 weeks following discharge. Strategies to encourage adherence to the home program include contact via telephone and email.

Sponsors

Allison Mandrusiak
Lead SponsorIndividual

Study design

Allocation
Randomised controlled trial
Intervention model
Parallel
Primary purpose
Treatment
Masking
Blinded (masking used)

Eligibility

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

Inclusion criteria

Diagnosis of Cystic Fibrosis; Hospitalised due to acute exacerbation of respiratory symptoms; Cognitively and physically able to perform the study tasks.

Exclusion criteria

Musculoskeletal impairments (present or in the twelve months preceding testing).

Outcome results

None listed

Source: ANZCTR · Data processed: Feb 4, 2026