NCT05608759Completed
Exercise Prehabilitation for Patients With NSCLC Before Surgery
Effect of a Home-based, Supervised Prehabilitation With Wearable Technology for Patients With Non-small Cell Lung Cancer Before Lung Resection: a Single-arm, Prospective Study
Source: ClinicalTrials.gov · Last updated 16 Jun 2026
Brief summary (registry, in English)
To explore the safety and compliance of a wearable telemedicine device that can receive basic vital signs in real time, and its active supervision mode with real-time adjustment of exercise prescription for preoperative prehabilitation exercises in patients at home; and to evaluate the effectiveness of preoperative prehabilitation exercises in a telemedicine active supervision mode in patients undergoing thoracoscopic lung tumour resection, taking into account the patient's cardiopulmonary exercise test, postoperative complications and quality of life scores.
- Status (registry)
- Completed
- Study type
- Interventional
- Enrollment
- 30 (actual)
- First submitted
- 27 Oct 2022
- Start date
- 1 Nov 2022
- Primary completion date
- 31 Dec 2024
- Lead sponsor
- Tongji Hospital
- Diseases
- Lung cancer
- NCT number
- NCT05608759
What you commit to
- Study type: Interventional
- Participants enrolled: 30
- From 1 Nov 2022 to the primary completion date, 31 Dec 2024
- 1 site in 1 country
- Visits and tests: ask the trial team, the registry does not list them
Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.
Who cannot take part
Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.
Other illness
- Patients who have a major medical or psychiatric disorder that is expected to affect exercise.
Other
- Known contraindication for cardiopulmonary exercise testing.
- Pregnancy or lactating women.
Who the study is looking for
- Capacity to give informed consent.
- Are able to tolerate surgery (i.e., segmentectomy, lobectomy) as indicated by standard clinical pre-op evaluation, including pulmonary function tests and cardiopulmonary exercise testing.
- Patients who can use a smartphone application.
- Patients who are diagnosed of stage I or II Non-small-cell lung carcinoma (NSCLC) diagnosis, with or without pre-operative histologic confirmation.
- Patients who can perform an exercise program for at least 4 weeks from the first visit to the preoperative clinic to elective surgery.
Age in the registry: 18 years to - · Sex: All · Does not accept healthy volunteers
Sites (1)
Sites in registry order. Pick your city on the disease page to sort them by distance.
| Site | City | Country | Site status |
|---|---|---|---|
| Tongji Hospital Coordinator of this site? Confirm its status | Wuhan | China | Unknown status |
This page is information, not medical advice. Discuss any trial with your doctor.