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Utilizing a Digital Tracking and Feedback System to Manage Patients with Chronic Obstructive Pulmonary Disease: a Multicenter Prospective Cohort Study

utilizing a digital tracking and feedback system to manage patients with chronic obstructive pulmonary disease: a multicenter prospective cohort study

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2300069170
Enrollment
Unknown
Registered
2023-03-08
Start date
2023-03-01
Completion date
Unknown
Last updated
2023-05-22

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

Conditions

Chronic Obstructive Pulmonary Disease

Interventions

pMDI digital intervention group:pMDI intelligent drug use sensor and digital software for COPD
pMDI control group:pMDI intelligent drug use sensor
DPI/SMI digital intervention group:digital software for COPD
DPI/SMI control group:No intervention

Sponsors

Tianjin Chest Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: Subjects who met all the following criteria were included in this study. (1) fully understand and sign the written informed consent. (2) patients with chronic obstructive pulmonary disease who meet the diagnostic criteria of the guidelines for the diagnosis and treatment of chronic obstructive Pulmonary Disease (2021 revised Edition). (3) permanent residents whose patients were = 18 years old when they were enrolled in the group. (4) the patients were in stable phase of COPD at the time of entering the group, and were given inhaled drug maintenance therapy.

Exclusion criteria

Exclusion criteria: Subjects will not be included in this study if they meet any of the following criteria. (1) Women during pregnancy or lactation. (2) there is cognitive disorder, which the researchers believe will affect the completion of the study. (3) there were rapidly progressive or unstable cardiovascular diseases, active pulmonary tuberculosis, neuromuscular diseases, immune system diseases and hematological diseases. (4) A history of allergy or intolerance to any component of sensor Acrylonitrile Butadiene Styrene resin material (similar to TV shell material).

Design outcomes

Primary

MeasureTime frame
Compliance with inhalation medication;

Secondary

MeasureTime frame
Acute exacerbation of COPD;

Countries

China

Contacts

Public ContactXiaoyun Zhao

Tianjin Chest Hospital

zxydoctor@163.com18002093080

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026