Ireland
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Impact of a Telerehabilitation-based Therapeutic Exercise Program on Postoperative Recovery in Patients With Lung Cancer: A Randomized Controlled Trial.

NCT07861282 · tracked via the Priya Life Science Spain tracker
Phase
Not applicable
Started
2026-10
Last updated
2026-10-06

Condition(s) studied

Lung NeoplasmsThoracic Surgery Lung

Investigational drug(s) / intervention(s)

Therapeutic Exercise-Based TelerehabilitationUsual Postoperative Care

Therapeutic Exercise-Based Telerehabilitation: Participants will receive an 8-week telerehabilitation program delivered through the RehBody platform. The intervention includes 24 supervised therapeutic exercise sessions and 8 online clinical follow-up sessions. Exercise sessions incorporate aerobic training, strength exercises, respiratory muscle training, individualized progression, symptom monitoring, and adherence support. Participants will also receive usual postoperative care.

Usual Postoperative Care: Participants assigned to the control group will receive usual postoperative care routinely provided after thoracic surgery for lung cancer. This includes early mobilization, progressive ambulation according to individual tolerance, deep breathing exercises, active upper-limb and trunk mobility exercises, cough training with wound protection, and discharge recommendations for home-based recovery. No structured telerehabilitation or supervised exercise program will be provided after hospital discharge.

Study summary

Lung cancer is one of the leading causes of cancer-related morbidity and mortality worldwide. Thoracic surgery remains the treatment of choice for patients with early-stage disease; however, postoperative recovery is frequently associated with reduced functional capacity, decreased physical activity levels, pulmonary complications, dyspnea, and impaired quality of life. Early physiotherapy interventions are recommended to minimize these adverse outcomes, although access to postoperative rehabilitation services remains limited in many healthcare settings, including the Andalusian Public Health System.

Telerehabilitation has emerged as a promising strategy to improve access to rehabilitation services by delivering therapeutic exercise and clinical follow-up remotely. Previous studies have demonstrated that telerehabilitation is safe, effective, and cost-efficient across different clinical populations. However, evidence regarding its effectiveness in patients recovering from lung cancer surgery remains limited.

This single-blind randomized controlled trial aims to compare the effects of an eight-week telerehabilitation program based on therapeutic exercise with usual postoperative care in patients with lung cancer undergoing thoracic surgery. Participants allocated to the intervention group will receive 24 therapeutic exercise sessions and 8 online clinical follow-up sessions delivered through the Rehbody platform over an 8-week period. Outcomes will include functional capacity, dyspnea, physical activity level, postoperative pulmonary complications, and health-related quality of life.

The study is designed to address the following research question: In adults with lung cancer undergoing thoracic surgery (Population), does an eight-week therapeutic exercise-based telerehabilitation program (Intervention), compared with usual postoperative care (Comparison), improve postoperative recovery as measured by functional capacity, dyspnea, physical activity level, postoperative pulmonary complications, and quality of life (Outcomes)?

Eligibility

Sex
ALL
Min age
18 Years
Max age
80 Years
Healthy volunteers
No
Inclusion Criteria: * Adults aged 18 to 80 years. * Histologically confirmed primary lung cancer (stage 0 to IIIB). * Patients who have undergone thoracic surgery for lung cancer. * Medical clearance to participate in an exercise-based rehabilitation program. * Ability to understand and communicate verbally. * Access to a smartphone and/or computer with internet connection. Exclusion Criteria: * Any medical condition or comorbidity that contraindicates participation in an exercise program. * Current psychiatric disorder that may interfere with study participation. * Inability to provide written informed consent. * Previous thoracic surgery. * History of another malignancy within the past five years.

Primary outcome measure(s)

  • Functional Capacity — Baseline (pre-surgery), 8 weeks (post-intervention), and 12 weeks (4-week follow-up)
    Functional capacity will be assessed using the One-Minute Sit-to-Stand Test (1MSTS). Participants will be instructed to stand up and sit down from a standardized chair as many times as possible within one minute. The total number of completed repetitions will be recorded, with higher scores indicating better functional capacity.

Trial sites (1)

FacilityCityRegionStatus
Hospital Universitario Virgen Macarena Seville Andalusia
Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT07861282 on ClinicalTrials.gov ↗ ← All trials in Spain