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Clinical application study of IoT combined with ventilator training for rehabilitation of patients with type II respiratory failure and chronic obstructive pulmonary disease

Clinical application study of IoT combined with ventilator training for rehabilitation of patients with type II respiratory failure and chronic obstructive pulmonary disease

Status
Active, not recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR1900026173
Enrollment
Unknown
Registered
2019-09-24
Start date
2019-10-20
Completion date
Unknown
Last updated
2019-09-30

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

Internet of things monitoring group:Internet of things monitoring
Ventilator training group:Ventilator training group
Combined exercise group:The Internet of things and the ventilator
Control:Normal processing

Sponsors

Zhongshan Hospital Affiliated Fudan University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
40 Years to 70 Years

Inclusion criteria

Inclusion criteria: 1. Patients who meet the guidelines for diagnosis, grading, and staged diagnosis, and whose blood gas analysis in the last two months meets type 2 respiratory failure are included in the patient; 2. Aged 40 to 80 years; 3. Received the treatment of standardized bronchodilators; 4. Did not participate in or are participating in other pulmonary rehabilitation studies or other influential studies.

Exclusion criteria

Exclusion criteria: 1. Checking for chronic cough caused by factors such as tuberculosis, fungi, tumors, irritating gas allergies, etc.; 2. Patients with other respiratory diseases that may cause asthma or difficulty breathing; 3. Pregnant or lactating women, allergic to the drug; 4. Combined with serious primary diseases such as cardiovascular, liver, kidney and hematopoietic system, diabetes, and mental patients; 5. Complicated by severe cardiac dysfunction; 6. Patients who are treated with other diseases; 7. Containing factors affecting the observation of efficacy.

Design outcomes

Primary

MeasureTime frame
SGRQ;mMRC;CAT;lung function;6MWT;SAS;SDS;Number of acute exacerbations;

Countries

China

Contacts

Public ContactShanqun Li

Zhongshan Hospital Affiliated to Fudan University

li.shanqun@zs-hospital.sh.cn+86 18616880856

Outcome results

None listed

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