Actively Recruiting

Age: 5Years - 17Years
All Genders
ID07129616

Remote Monitoring of Asthma in Children and Young People - Reducing Risk of Asthma Attack Using a Connected Patient Approach

Led by University of Edinburgh · Updated on 2026-01-22

900

Participants Needed

1

Research Sites

21 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

This research aims to evaluate whether healthcare data combined with remotely collected patient data can accurately predict asthma attacks in children and young people aged 5 to 17 years. The study focuses on reducing asthma attacks compared to historic averages by monitoring a whole population of children and young people with asthma. A subgroup at high risk will participate in a detailed study involving remote monitoring. The study uses a new risk stratification system including a clinician dashboard and a patient-facing app. The dashboard allows clinicians to identify individuals at increased risk of asthma attack based on healthcare data and remote monitoring, such as night cough and symptom scores. Identified high-risk patients receive clinical interventions like phone calls or appointments, and may be offered an enhanced app to monitor symptoms, cough, and activity. Participants' routine healthcare data will be monitored continuously, with those at high risk contacted for clinical review. Data collected include medication prescriptions, hospital admissions, lung function, and app-generated symptom and cough data. Outcomes measured over six months include the number of asthma attacks, hospitalizations, symptom rates, interventions, and app usage. Data privacy and security are maintained throughout the study, which runs from November 2025 to March 2027.

CONDITIONS

Brief Title

Remote Monitoring of Asthma in Children and Young People

Who Can Participate

Age: 5Years - 17Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Children and young people aged 5 to 17 years
  • Diagnosis of asthma or suspected asthma
  • Prescription of inhaled corticosteroid in the prior 2 years
Not Eligible

You will not qualify if you...

  • Alternative non-asthma diagnosis requiring inhaled steroids
  • Diagnosis of cystic fibrosis
  • Diagnosis of bronchiectasis
  • Diagnosis of primary ciliary dyskinesia

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

1 visit (in-person)

Monitoring

Duration - Up to 6 months

Participants with asthma are continuously monitored using a clinician dashboard that applies a risk algorithm to assess their risk of an asthma attack. This includes reviewing healthcare data and patient-reported information to identify those at increased risk.

Weekly remote monitoring with clinician review

Clinical Intervention

Duration - Ongoing throughout the 6-month monitoring period

Participants identified as high risk receive clinical interventions such as phone calls or appointments to assess and manage asthma control. Interventions are tailored by clinicians based on risk status.

Phone calls or clinic appointments as needed, typically within 1 week of risk identification

App Usage and Remote Symptom Monitoring

Duration - Up to 6 months

High-risk participants are offered access to a patient-facing app to report symptoms, monitor night-time cough, and track activity. This supports ongoing asthma management and risk stratification.

Continuous daily symptom reporting and app engagement remotely

Trial Site Locations

Total: 1 location

1

NHS Lothian

Edinburgh, United Kingdom

Actively Recruiting

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Research Team

K

kenneth a macleod, MbChB, PhD

How is the study designed?

Study Type

OBSERVATIONAL

Masking

N/A

Allocation

N/A

Model

N/A

Primary Purpose

N/A

Number of Arms

2

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