pneumoconiosis
Conditions
Interventions
Gold Standard:The actual situation of the subjects during the experiment.
Index test:The subject wears a Vivalink's wearable ECG patch on the left front chest and uses the patch to collect chest surface vibration acceleration and ECG signals.
Sponsors
Shanghai Pulmonary Hospital, Tongji Univiersity
Eligibility
Sex/Gender
All
Age
18 Years to 80 Years
Inclusion criteria
Inclusion criteria: 1. Patients meeting the diagnostic criteria of pneumoconiosis; 2. Aged 18-80 years old, no restriction on gender; 3. No other respiratory or other systemic diseases that can cause cough detection abnormalities at the time of screening; 4. No significant cognitive impairment at the time of screening; 5. Good eyesight or hearing (glasses and hearing aids can be worn), able to cooperate with the investigator's instructions; 6. Not participating in other clinical trials.
Exclusion criteria
Exclusion criteria: 1. Patients with liver or kidney failure; 2. Patients with cardiac insufficiency; 3. Patients with multiple organ failure; 4. Patients with malignant tumors or undergoing anti-tumor treatment; 5. Patients with dyskinesia caused by heart, nervous system, bone and joint system diseases; 6. Female subjects of childbearing age during pregnancy and lactation; 7. Patients with cognitive impairment or mental problems who cannot cooperate with the trial; 8. Patients who are not eligible to participate in clinical trials according to the investigator, including those with existing physical or psychological conditions that preclude adherence to the protocol.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| the chest surface vibration acceleration;Consistency between the chest surface vibration acceleration collected and the actual occurrence; | — |
Secondary
| Measure | Time frame |
|---|---|
| respiratory symptoms; | — |
Countries
China
Contacts
Public ContactLing Mao
Department of Pneumoconiosis, Shanghai Pulmonary Hospital affiliated to Tongji University
Outcome results
None listed