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Therapist-made bubble-positive expiratory pressure: a survey of physiotherapists in Australia

Use of the Bottle/Bubble Positive Expiratory Pressure (PEP) device by Physiotherapists in Australian hospitals for treating people with respiratory disorders.

Status
Completed
Phases
Unknown
Study type
Observational
Source
ANZCTR
Registry ID
ACTRN12612000736842
Enrollment
107
Registered
2012-07-10
Start date
2012-07-25
Completion date
2013-05-31
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

It is believed that physiotherapists in Australia use the Bottle/Bubble PEP device to treat patients that have secretion clearance problems. It is unknown though to what extent it is used or the rationale behind its use. This questionnaire will assist in answering these questions at it will be sent to a representative sample of physiotherapists working in hospitals within Australia.

Interventions

The study will use a questionnaire that will be sent to all specialist paediatric hospitals in Australia and to a representative sample of public and private hospitals in Australia. The physiotherapists working in these hospitals will be invited to participate in the study. The aims of the questionnaire are to determine: 1) the extent of the Bottle/Bubble PEP use in Australia; 2) the proposed rationale for its use; 3) for which patients Bottle/Bubble PEP is used and; 4) why it is chosen rather

The study will use a questionnaire that will be sent to all specialist paediatric hospitals in Australia and to a representative sample of public and private hospitals in Australia. The physiotherapists working in these hospitals will be invited to participate in the study. The aims of the questionnaire are to determine: 1) the extent of the Bottle/Bubble PEP use in Australia; 2) the proposed rationale for its use; 3) for which patients Bottle/Bubble PEP is used and; 4) why it is chosen rather than other PEP devices. The questionnaire is to be returned 1 month after it is mailed out. If the questionnaire is not returned after a month, respondents will be invited again to participate in the study. Maximum length of this study is 6 months.

Sponsors

Mary Santos
Lead SponsorIndividual

Eligibility

Sex/Gender
All
Age
0 to No maximum
Healthy volunteers
Yes

Inclusion criteria

Physiotherapists in Australia that treat people with respiratory disorders.

Exclusion criteria

Physiotherapists not treating people with respiratory disorders; non-physiotherapists

Outcome results

None listed

Source: ANZCTR · Data processed: Feb 4, 2026