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Asthma Self ManagementNCT06900361

Use of Mobile Phone Application for Asthma Sele Management

An observational study of Asthma Self Management, run by Kamuzu University of Health Sciences at 1 site in Malawi.

Completed

Finished. The study has ended and is not enrolling. Results may be posted on the official record.

Official record
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Trial summary

This study aimed to assess the feasibility and acceptability of self-management provided through a mobile application. Read more about this study

Who is it for?
Ages 10 to 18 yearsHealthy volunteers can take part
Conditions the study is for
Asthma Self Management
How many people
17 participants
Where
1 siteMalawi
Study dates
11 Nov 2020to 30 Dec 2021
Phase
Observational
Are there results?
None posted in the registry

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 10 to 18 years
  • All sexes
  • Healthy volunteers accepted
  • Child, Adult

Study population: All asthma patients aged 10 years and over attending pediatric outpatient clinic.

Who may be able to join

  • Be aged 10 years and over
  • Have a Physician diagnosis of asthma and be prescribed a salbutamol inhaler
  • Reside in Blantyre
  • Participants should be able to read and write either English or Chichewa with Minimum standard 5 eductaion

Who cannot join

  • Cognitively impaired
  • Presence of coormobities
  • Refues to consent
  • Presence of active lung disease other than athsma

Trial locations and contacts

1 site in 1 country.

Malawi1 site
  • Kamuzu University of Malawi

    Blantyre

Other trials in Malawi

About this study

Official title: Feasibility and Acceptability of Asthma Self-Management Delivered Through a Mobile Phone Application: A Pilot Study in Malawi

This study aimed to assess the feasibility and acceptability of self-management provided through a mobile application.

Read the detailed description

The chronic nature of asthma management requires a long-term approach taking into account the variability of disease symptoms, triggers and exacerbations. Several current guidelines advocate for self-management as part of standard care. Low-income countries (LMICs) such as Malawi are experiencing an increase in the burden of disease which hinders delivery of self-management services. Mobile phone health applications (mHealth) has been reported as an effective and cost-effective tool in the monitoring and management of asthma.

Keywords
Asthma Self Management

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. GINA Symptom Control Assessment

    Asthma Control Test (ATC) Score

    Measured: one year

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted28 Mar 2025
  2. Study start11 Nov 2020
  3. Primary completion30 Dec 2021
  4. Study completion30 Dec 2021

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Observational
Observational model
Other
Time perspective
Other
Enrolment
17 participants (actual)
IDs, dates and publications
ClinicalTrials.gov ID
NCT06900361
Sponsor's protocol ID
P.09/20/3132
Other IDs
5U24HL136791
Status last verified
Mar 2025
First submitted
26 Mar 2025
Last updated
28 Mar 2025
Results posted
No
Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
Yes: The de-identified datasets used and/or analyzed during the current study are available from the corresponding author on reasonable request.

Publications

  • Global Initiative for Asthma. Global Strategy for Asthma Management and Prevention,2019. Available from www.ginasthma.org

Questions about this trial

What is this clinical trial studying?

An observational study of Asthma Self Management, run by Kamuzu University of Health Sciences at 1 site in Malawi.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 4 inclusion and 4 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: finished, as of the sponsor's last update on 28 Mar 2025. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in Malawi. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.

How can a doctor refer a patient or contact the research team?

The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

GINA Symptom Control Assessment (time frame: one year). It is what the study was designed to measure, not a finding.

Where can I read the original study information?

On the ClinicalTrials.gov record for NCT06900361, which also lists 1 linked publication.

Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 28 Mar 2025.

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