Skip to content

Comparison of supervised home-based tele-pulmonary rehabilitation with traditional center-based rehabilitation: a non-inferiority randomized controlled trial

Comparison of supervised home-based tele-pulmonary rehabilitation with traditional center-based rehabilitation: a non-inferiority randomized controlled trial

Status
Recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2300076969
Enrollment
Unknown
Registered
2023-10-25
Start date
2024-04-01
Completion date
Unknown
Last updated
2024-07-08

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

Supervised remote home-based pulmonary rehabilitation group.:Exercise training (aerobic exercise, resistance training, respiratory muscle training), education, nutritional support, and psychological a
Traditional center-based pulmonary rehabilitation group.:Exercise training (aerobic exercise, resistance training, respiratory muscle training), education, nutritional support, and psychological and b

Sponsors

General Hospital of Ningxia Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
40 Years to 80 Years

Inclusion criteria

Inclusion criteria: 1. Patients aged 40-80 years old, male or female, with or without smoking history, from the community, outpatient or hospitalized settings; 2. Patients with an mMRC scale score of 1 or higher; 3. Patients who were able to communicate effectively in either language or text and had the capability to complete any necessary ancillary examinations; 4. Patients who had obtained informed consent and received approval from the Ethics Committee; 5. Patients or their family members who had access to smartphones and were capable of interacting effectively with doctors through WeChat; 6. Patients who had not experienced an acute exacerbation of the disease within the previous month.

Exclusion criteria

Exclusion criteria: 1. Unstable angina or arrhythmia, as well as unstable fractures; 2. Clinical diagnosis of lung cancer, bronchiectasis, pneumoconiosis, or other chronic respiratory diseases; 3. Hematological diseases or malignant tumors that could hinder the completion of the research; 4. Infectious diseases that pose a risk to others and have no isolation measures in place; 5. Severe cognitive impairment; 6. Unwillingness of either the patient or their family members to participate in the study; 7. Current participation in or previous participation in any form of pulmonary rehabilitation within the past 6 months; 8. Lack of access to a smartphone.

Design outcomes

Primary

MeasureTime frame
6 minutes walking distance varies, 6MWT;

Secondary

MeasureTime frame
1 minute sitting and standing test, 1-min STST;Lung function;Respiratory muscle strength;Quality of Life (CAT);Shortness of breath symptoms (mMRC);Mental state (HAD);Acute exacerbation;Readmission rate;Diaphragm ultrasound;Subcutaneous chest fat, intermuscular fat, chest wall muscle volume, and quality;Exercise prescription completion rate and incidence of adverse events;

Countries

China

Contacts

Public ContactJuan Chen

General Hospital of Ningxia Medical University

13014292231@163.com+86 130 1429 2231

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 6, 2026