Clinical trial · Interventional
Postoperative Telerehabilitation in Older Adults
Comparison of Postoperative Telerehabilitation and Unsupervised Home-Based Training in Older Adults With Lung Cancer: A Randomized Controlled Trial
NCT05435885CI-TRIAL-00091105completedN/AResults postedClinicalTrials.gov clinicaltrialsProvenance
- Source
- ClinicalTrials.gov
- Retrieved
- Sep 8, 2026
- Layer
- normalized (units and labels harmonized; values unchanged)
- Run
- ING-CLINICALTRIALS-20260908-000001
Summary
Brief summary (as posted)
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.
Conditions
Conditions (3)
Free-text conditions as registered, with the CancerIndex entity they were reconciled to and the match type.
| Condition (as posted) | Mapped entity | Match | Confidence |
|---|---|---|---|
| Carcinoma, Non-Small-Cell Lung | Lung Non-Small Cell Carcinoma | ALIAS | 0.90 |
| Cardiopulmonary Exercise Test | — | UNRESOLVED | — |
| Telerehabilitation | — | UNRESOLVED | — |
Interventions
Interventions (2)
| Intervention | Type | Mapped drug | Match |
|---|---|---|---|
| Control (Education) | Other | — | UNRESOLVED |
| Pulmonary Tele-Rehabilitation | Other | — | UNRESOLVED |
Design
Arms and outcomes
Arms (2)
- type
- EXPERIMENTAL
- label
- Tele-rehabilitation group
- description
- The Tele-rehabilitation group performs 12 training sessions during four weeks. (3 sessions/week)
- interventionNames
- Other: Pulmonary Tele-Rehabilitation
- type
- OTHER
- label
- Control group
- description
- The control group receives usual care with only one educational session.
- interventionNames
- Other: Control (Education)
Primary outcomes (1)
- measure
- Change From Baseline in VO2 Peak (Peak Oxygen Uptake, mL/kg/Min) on the CardioPulmonary Exercise Test(CPET) After 4 Weeks Intervention
- timeFrame
Eligibility
Eligibility (as posted)
- Sex
- All
- Minimum age
- 65 Years
Show eligibility criteria text
Inclusion Criteria: 1. A person who is suspected of lung cancer and is scheduled to undergo a thoracoscopic lung resection surgery. 2. men and women the age ≥65 years. 3. A person who understands the course of the clinical trial and signs the informed consent form. Exclusion Criteria: 1. Patients whose activity is restricted due to other diseases (e.g. osteoarthritis, spinal disease, cerebral infarction, etc.) 2. Patients who cannot test bioimpedance analysis due to the insertion of artificial pacemakers and defibrillators 3. A person who has difficulty judging himself/herself due to dementia, etc 4. Those enrolled in other clinical trials 5. A person deemed inappropriate to participate in this clinical trial under the judgement of the investigator. 6. A person who cannot use mobile messenger
References
Publications (1)
- DERIVEDShin YB, Huh S, Cho JS, Hong CH, Kim Y, Shin MJ, Yun RY, Lee J, Son BS, Kim SH. Comparison of Postoperative Telerehabilitation and Unsupervised Home-Based Training in Older Adults With Lung Cancer: A Randomized Controlled Trial. J Cardiopulm Rehabil Prev. 2026 Mar 1;46(2):132-139. doi: 10.1097/HCR.0000000000000988. Epub 2025 Nov 26. PMID 41294889