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Clinical Trials in Taiwan / NCT06432634
Enrolling by invitation Not applicable

Effects of CPRP on Patients Undergoing Lung Resection

NCT06432634 · tracked via the Priya Life Science Taiwan tracker
Phase
Not applicable
Started
2024-11-15
Last updated
2025-09-02

Condition(s) studied

Rehabilitation

Investigational drug(s) / intervention(s)

Standard careComprehensive pulmonary rehabilitation programs

Standard care: The pre-operative educational session has a duration of 40 minutes and covers pre-operative education, breathing exercises (diaphragmatic breathing, deep breathing techniques and sustained maximal inflation), and airway clearance techniques (directed cough, huffing, and chest physiotherapy). Patients are instructed to perform these techniques ten times per waking hour, every day. The in-patient peri-operative session incorporates intermittent positive pressure breathing inhalation (IPPB) administered for 15 minutes twice daily. Inhalation therapy involving mucolytics and bronchodilators is administered three times per day, and early mobilization is encouraged until discharge. Upon discharge, participants are encouraged to continue practicing breathing exercises, deep breathing techniques, and maintaining an active level of activity.

Comprehensive pulmonary rehabilitation programs: 1. Warm-up and cool-down exercises: stretching various muscle groups for a duration of 15 to 20 minutes and a slow 3-minute walk 2. Aerobic training: using a lower-limb cycle ergometer for a duration of 30 to 40 minutes. Initiated warm-up at 0 wattages for 5 minutes. Incrementally increased wattages within 5-10 minutes until reaching the 40-80% heart rate reserve or 4 to 6 of modified Borg scale for at least 20 minutes. Concludes with a 5-minute cool-down period at 10 wattages. 3. The resistance training involves both upper and lower limbs: (1) Upper Limb Resistance Training: Shoulder lift, abduction, and horizontal abduction exercises are performed. Each exercise is repeated for three sessions comprising 10 repetitions each. A 0.5-2 kg dumbbell is utilized for resistance. (2) Lower Limb Resistance Training: Sit-to-stand exercises are performed. Each session consists of three sets of 10 repetitions.

Study summary

The aim of this project is to investigate the effectiveness of implementing a Comprehensive Pulmonary Rehabilitation Program (CPRP) in patients undergoing lung resection surgery. The CPRP encompasses a training regimen combining aerobic exercise, resistance exercises, breathing exercises, and home activities, specifically tailored for patients with limited exercise capacity and impaired lung function. The study seeks to understand the physiological and biological effects of the CPRP in this patient population.

Eligibility

Sex
ALL
Min age
20 Years
Max age
—
Healthy volunteers
No
Inclusion Criteria: * Adults (age ≥ 20 years old) * Receiving lung resection surgery * At least one of the following: 6MWD \< 500 meters, oxygen saturation by pulse oximetry (SpO2) drop ≥ 4% or SpO2\< 90% during 6MWT, pre-operative forced expiratory volume in 1 second (FEV1) or forced vital capacity (FVC) ≤ 80% of predicted value or FEV1/FVC ratio ≤ 0.7 * Able to walk autonomously without mobility aids * Written informed consent Exclusion Criteria: * Neoadjuvant therapy with chemo- or radiotherapy in the six months prior to surgery * Received pulmonary rehabilitation programs six months prior to surgery * Previous lung resection * Inability to perform the exercise training * Instability in cardiovascular disease, neurological disorders, or musculoskeletal conditions * Have cognitive deficits with potential severe impact on compliance * Do not provide written informed consent

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
Chang Gung Memorial Hospital Chiayi City Taiwan

More Chang Gung Memorial Hospital trials in Taiwan

Other trials for the same condition

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 NCT06432634 on ClinicalTrials.gov ↗ ← All trials in Taiwan