A Personalized Mobile Application Providing Temperature-Related Health Risk Warnings and Protective Recommendations for Patients With Chronic Obstructive Pulmonary Disease

Trial statusNot yet recruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age40-80
SponsorTiantian Li

About this trial

This study will test whether a personalized mobile application that provides temperature-related health risk warnings and protective recommendations can reduce acute exacerbations in people with chronic obstructive pulmonary disease (COPD). Researchers will compare participants who receive the mobile application in addition to usual care with those who receive usual care alone. The main question is whether the mobile application reduces the number of COPD acute exacerbation events over 12 months. The study will also evaluate secondary outcomes including quality of life, functional capacity, symptoms, psychological status, physiological and biochemical indicators, environmental temperature risk perception, and participants' use of the mobile application.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

Tertiary hospitals;

Hospitals with respiratory wards that admit patients with COPD;

Hospitals with a well-established electronic health record system and follow-up capability;

Hospitals able to assign a study coordinator.

Disqualifiers

Primary hospitals or private hospitals;

Hospitals unable to cooperate with the study protocol.

Patients with asthma;

Women who are known to be pregnant or breastfeeding, or who have a positive pregnancy test before cluster randomization;

Trial design

Design model

Parallel

Treatments tested in this trial

  • Mobile Application-Based Personalized Temperature Health Risk Early Warning Intervention

    Other intervention

    This study implements a digital early warning intervention targeting personalized temperature-related health risks. The mobile application integrates real-time meteorological data and individual characteristics to generate risk levels and deliver tailored health alerts and guidance aimed at supporting risk management and reducing exposure-related health risks.

Treatment groups

240 Participants
are divided into 2 treatment groups
Group A: Personalized Temperature Risk Intervention + Usual COPD CareExperimental treatment 1 intervention
Group B: Usual COPD CareNo intervention 0 interventions

Trial outcomes

Primary outcomes

1

Number of COPD Acute Exacerbations

Total number of acute exacerbations of COPD managed at home, via outpatient visits, emergency department visits, or hospitalizations.

Time frame
12 months after baseline

Secondary outcomes

1

Number of Home-managed COPD Acute Exacerbations

Number of home-managed COPD acute exacerbations

Time frame
6 and 12 months after baseline
2

Number of Outpatient-managed COPD Acute Exacerbations

Number of outpatient-managed COPD acute exacerbations

Time frame
6 and 12 months after baseline
3

Number of Emergency Department-managed COPD Acute Exacerbations

Number of emergency department-managed COPD acute exacerbations

Time frame
6 and 12 months after baseline
4

Number of Hospitalized COPD Acute Exacerbations

Number of hospitalized COPD acute exacerbations

Time frame
6 and 12 months after baseline

Other outcomes

Locations

This trial has no locations.

Sponsors and contacts

Click on the lead sponsor to view all of their trials.

Tiantian Li

Lead sponsor

Centers for Disease Control and Prevention, China

Sponsor institution

This trial is not recruiting at the moment. You can still explore other options: