N/A
N=64
Postoperative Telerehabilitation in Older Adults
Telerehabilitation · Carcinoma, Non-Small-Cell Lung · Cardiopulmonary Exercise Test
Bottom Line
View on ClinicalTrials.gov: NCT05435885 ↗Enrolled (actual)
64
Serious AEs
0.0%
Results posted
Jun 2025
Primary outcome: Primary: Change From Baseline in VO2 Peak (Peak Oxygen Uptake, mL/kg/Min) on the CardioPulmonary Exercise Test(CPET) After 4 Weeks Intervention — 23.67; 23.09; 19.28; 20.41 mL/kg/min
Study Design & Population
- Study type
- Interventional
- Phase
- N/A
- Interventions
- Pulmonary Tele-Rehabilitation (Other); Control (Education) (Other)
- Age
- Older Adult · 65+ yrs
- Sex
- All
- Sponsor
- Pusan National University Hospital
- Primary completion
- Feb 2024
Outcome Measures
| Outcome | Result | p-value |
|---|---|---|
| PRIMARY Change From Baseline in VO2 Peak (Peak Oxygen Uptake, mL/kg/Min) on the CardioPulmonary Exercise Test(CPET) After 4 Weeks Intervention |
23.67; 23.09; 19.28; 20.41; 21.85; 19.85 | — |
| SECONDARY Ventilatory Efficiency (VE/VCO₂ Slope) |
4.0; 0.6; -0.1; 1.4 | — |
| SECONDARY Maximal Inspiratory Pressure (MIP) |
5.2; 8.3; 7.9; 5.4 | — |
| SECONDARY Skeletal Muscle Index (SMI) |
0.1; -0.1; 0.1; 0.11 | — |
| SECONDARY Hospital Anxiety and Depression Scale (HADS) |
-0.4; 0.6; -0.9; -0.1; -1.1; -0.6 | — |
| SECONDARY EQ-5D (EuroQol-5 Dimension) |
0.05; -0.03; 0.05; 0.0; 6.4; 5.4 | — |
| SECONDARY Grip Strength |
-0.3; 0.1; -0.7; -0.2 | — |
| SECONDARY Steps |
-45; -469; 1050; 95 | — |
| SECONDARY Peak Expiratory Flow (PEF) |
14.2; 27.4; 28.7; 24.1 | — |
| SECONDARY Forced Vital Capacity (FVC) |
0.17; 0.18; 0.25; 0.23 | — |
| SECONDARY The Forced Expiratory Volume in 1 Second (FEV1) |
0.14; 0.11; 0.19; 0.15 | — |
| SECONDARY Whole-Body Phase Angle |
0.04; -0.1; -0.02; -0.12 | — |
Summary
The purpose of this study is to confirm the effectiveness of a mobile messenger-based home tele-rehabilitation protocol in patients who have undergone lung resection surgery.
By analyzing the difference from the existing postoperative pulmonary rehabilitation, the investigators would like to propose a new pulmonary tele-rehabilitation protocol.
Eligibility Criteria
Inclusion Criteria
- A person who is suspected of lung cancer and is scheduled to undergo a thoracoscopic lung resection surgery.
- men and women the age ≥65 years.
- A person who understands the course of the clinical trial and signs the informed consent form.
Exclusion Criteria
- Patients whose activity is restricted due to other diseases (e.g. osteoarthritis, spinal disease, cerebral infarction, etc.)
- Patients who cannot test bioimpedance analysis due to the insertion of artificial pacemakers and defibrillators
- A person who has difficulty judging himself/herself due to dementia, etc
- Those enrolled in other clinical trials
- A person deemed inappropriate to participate in this clinical trial under the judgement of the investigator.
- A person who cannot use mobile messenger
Data sourced from ClinicalTrials.gov (NCT05435885). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication.