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Perioperative tele-rehabilitation in elderly patients undergoing pneumonectomy:a randomized controlled trial

Application of artificial intelligence system based on remote technology in rehabilitation assessment and training of chronic diseases

Status
Active, not recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2300074463
Enrollment
Unknown
Registered
2023-08-08
Start date
2023-08-12
Completion date
Unknown
Last updated
2023-08-21

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

Conditions

lung cancer

Interventions

Control group:Give perioperative rehabilitation guidance once in the outpatient department and corresponding text materials
Intervention group:Push the content of perioperative tele-rehabilitation every day for a total of 6 weeks

Sponsors

Chinese Academy of Medical Sciences & Peking Union Medical College
Lead Sponsor

Eligibility

Sex/Gender
All
Age
60 Years to 90 Years

Inclusion criteria

Inclusion criteria: 1. Age = 60y; 2. Non-small cell lung cancer patients who plan to undergo thoracoscopic pneumonectomy; 3. There is at least one week or more to the operation day; 4. Be able to sign informed consent independently 5. Be able to use the remote rehabilitation training system (including with the support of family members) 6. Be able to cooperate with the research doctor to follow up on time

Exclusion criteria

Exclusion criteria: 1. Pathologically confirmed that it is not a patient with non-small cell lung cancer; 2. Those with severe cognitive impairment, hearing or visual impairment who cannot complete sports training 3. Researchers who have other serious nervous system diseases, motor system diseases, heart, lung, liver and kidney diseases, uncontrolled hypertension, uncontrolled metabolic diseases, and other malignant tumors think they are not suitable to participate in this research 4. It is also difficult to stand or walk with the help of auxiliary equipment

Design outcomes

Primary

MeasureTime frame
6 min walking test;

Secondary

MeasureTime frame
Maximum inspiratory/expiratory pressure;gripping power;Quadriceps strength;Stand up - walk timing test;Functional independence assessment scale(FIM);SF-36;GAD-7;PHQ-9;Postoperative pulmonary complications;Postoperative hospital stay;Postoperative extubation time;

Countries

China

Contacts

Public ContactLixia chen

Chinese Academy of Medical Sciences & Peking Union Medical College

clx727@126.com+86 136 9106 0078

Outcome results

None listed

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