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Personalized Mobile Phone Video Recording to Improve Inhaler Techniques in Asthma Patients.

A Randomized Control Trial to Evaluate the Effectiveness of Personalized Mobile Phone Video Recording in Addition to Standard Care Compared to Standard Care Alone in Improving Inhaler Technique Among Patients With Asthma. (RECORD)

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04503837
Acronym
RECORD
Enrollment
234
Registered
2020-08-07
Start date
2020-09-01
Completion date
2021-04-30
Last updated
2020-08-07

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

Conditions

Asthma

Keywords

inhaler technique, compliance

Brief summary

To investigate the effectiveness of addition of recording video of the patient performing inhaler techniques using mobile phone for discussion with the patient, to standard care inhaler education compared to standard care inhaler education alone, in improving inhaler technique of asthma patients.

Detailed description

This is a single-centre, randomized, controlled, parallel group, assessor-blinded trial to evaluate the effectiveness of Personalized Mobile Phone Video Recording in addition to standard care, compared to standard care alone, in improving inhaler technique among patients with asthma. Patients are randomised to either Personalized Video Recording with standard clinical practice group (intervention) or to standard clinical practice group (control) in 1:1 ratio. Subject's inhaler technique assessment is performed by using a standard checklist of steps according to the type of inhaler used by subject. All inhaler technique assessment and asthma control questionnaire will be administered before the intervention/control treatment by a blinded assessor. Both intervention and control treatment will be administered by the same investigators.

Interventions

PROCEDUREPersonalized Mobile Phone Video Recording

Subjects will be asked to perform inhaler technique while on video recording. The video will be shown to subjects immediately during technique education session and mistakes (if any) will be pointed out to subject.

Sponsors

Penang Hospital, Malaysia
Lead SponsorOTHER_GOV

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Outcomes Assessor)

Masking description

All outcome assessment - inhaler technique assessment and asthma control questionnaire will be administered by a blinded assessor.

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

1. 18 years old and above 2. Informed consent 3. Established clinical diagnosis of asthma by patient's treating doctor 4. Prescribed with inhalers (any type) for therapeutic indication for at least 3 months

Exclusion criteria

1. Unable to converse/understand Malay or English 2. Not able to perform inhalation on his/her own self 3. Using spacer/valved holding chamber in addition to MDI 4. Not able to comply with study procedures in the opinion of investigators 5. More than two different types of inhaler which require different techniques

Design outcomes

Primary

MeasureTime frameDescription
Inhaler Technique6 monthsCorrect inhaler technique (able to do all the steps of inhaler technique, as stipulated in checklist of subject's inhaler)

Secondary

MeasureTime frameDescription
Asthma Control1, 3 and 6 monthsMean score of Asthma Control Questionnaire (ACQ)
Inhaler Technique1 and 3 monthsCorrect inhaler technique (able to do all the steps of inhaler technique, as stipulated in checklist of subject's inhaler)
Inhaler Technique Error1, 3 and 6 monthsNumber of errors committed by patients according to checklist

Countries

Malaysia

Contacts

Primary ContactChoon Seong Ang, MBChB
angchoonseong@hotmail.com0103837286

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026