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Inhaler technique mastery and maintenance in general medical practitioners: Easy Low Instruction Over Time (Dr ELIOT)

Inhaler technique mastery and maintenance in general medical practitioners: Easy Low Instruction Over Time (Dr ELIOT)

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ANZCTR
Registry ID
ACTRN12618001478202
Acronym
Dr ELIOT
Enrollment
208
Registered
2018-09-04
Start date
2018-08-31
Completion date
2019-09-30
Last updated
2019-08-26

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

Conditions

None listed

Brief summary

Poor inhaler technique has been a major problem in managing respiratory illness for decades ; it compromises disease control and is associated with an increase in the economic burden of disease management. When inhaler technique education is delivered to general practitioners (GPs), it can improve attitudes and facilitate implementation of inhaler education into practice. The primary purpose of this study is to assess what level of education is minimally required to master inhaler technique in general practitioners and we hypothesize that inhaler technique mastery is not an intuitive skill.

Interventions

This study involves an intervention that is delivered on two occasions, one month apart (at Visit 1 and Visit 2). Each visit will take no longer than ten minutes. The intervention: At Visit 1, participants are given one of two placebo inhalers and are asked to use the inhaler. If they are not able to demonstrate correct inhaler technique, they will receive education in the form of written information; if then are still not able to use the inhaler after the written information, they will be shown

This study involves an intervention that is delivered on two occasions, one month apart (at Visit 1 and Visit 2). Each visit will take no longer than ten minutes. The intervention: At Visit 1, participants are given one of two placebo inhalers and are asked to use the inhaler. If they are not able to demonstrate correct inhaler technique, they will receive education in the form of written information; if then are still not able to use the inhaler after the written information, they will be shown a video on device technique and if following this they are still not able to demonstrate correct inhaler technique they will be given individualised education by the researcher. The same will be repeated for the other device. The same process (intervention) will be delivered with the same two devices at Visit 2 (1 month after Visit 1). The intervention will be delivered by researcher assistants from the Woolcock Institute of Medical Research. The two inhalers that will be used are Turbuhalers and Spiromax inhalers. Written instructions for their use have been developed by the research team and based on product information that is available to patients. Video instructions on inhaler use that will be used are publicly available on the National Asthma Council website for health care professional and patient use. The cross over nature of the study is in reference to GPs being asked to demonstrate use of 2 devices, one after the other. In consideration of the fact that receiving instruction on the use of the first inhaler may positively influence the intuitive use of the second inhaler, GPs will be randomly allocated to use of either inhaler first to accomodate for this bias. To ensure fidelity to the intervention, GPs inhaler technique is assessed by the researchers following each level of education until inhaler technique is mastered. The Turbuhaler placebo devices are empty and contain no active ingredients. The spiromax devices contains Lactose monohydrate with approximately 10mg delivered per inhalation.

Sponsors

Woolcock Institute of Medical Research
Lead SponsorOther

Study design

Allocation
Randomised controlled trial
Intervention model
Other
Primary purpose
Educational / counselling / training
Masking
Open (masking not used)

Eligibility

Sex/Gender
All
Age
18 Years to No maximum
Healthy volunteers
Yes

Inclusion criteria

• Informed consent is obtained before conducting any study related procedures. • The participant is a registered and practicing GP in NSW. • The participant must be willing and able to comply with study restrictions and to remain at the study site for the required duration during the study period, and willing to return to the site for the follow-up evaluation as specified in this protocol.

Exclusion criteria

Participants will be excluded from the study if they have asthma or COPD or use an inhaler themselves.

Outcome results

None listed

Source: ANZCTR · Data processed: Feb 4, 2026