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Clinical Trials in Portugal / NCT06968273
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Analysis of Muscle Oxygen Saturation and Functional Variables During Physical Capacity Assessments in Patients With COPD

NCT06968273 · tracked via the Priya Life Science Portugal tracker
Phase
Not applicable
Started
2025-05-02
Last updated
2025-05-13

Condition(s) studied

Chronic Obstructive Pulmonary Disease (COPD)Muscle OxygenationExerciseRespiratory Physiotherapy

Investigational drug(s) / intervention(s)

Combined respiratory physiotherapy and cardiovascular-strength training program

Combined respiratory physiotherapy and cardiovascular-strength training program: 20-session supervised hospital-based program including respiratory physiotherapy, aerobic training (guided by Borg scale and HR monitoring), and strength training using progressive loads (based on 1RM). Duration: 4 weeks (5 sessions/week).

Study summary

This experimental pre-post intervention study aims to evaluate the effect of a respiratory physiotherapy and combined strength and cardiovascular training program on muscle oxygen saturation and functional capacity in patients with Chronic Obstructive Pulmonary Disease (COPD). Oxygenation of the intercostal, quadriceps, and triceps surae muscles will be assessed using near-infrared spectroscopy (NIRS) during standard physical performance tests (6-Minute Walk Test and 30-Second Chair Stand Test). Additional functional parameters and quality of life will be recorded pre- and post-intervention. The results will contribute to optimizing rehabilitation programs and monitoring intensity and progress through muscle oxygenation data.

Eligibility

Sex
ALL
Min age
18 Years
Max age
—
Healthy volunteers
No
Inclusion Criteria: * Age ≥18 years * Clinical diagnosis of COPD * Medically cleared for physical exercise Exclusion Criteria: * Decompensated heart failure or exercise-limiting comorbidities * Cognitive impairment or legal incapacity to consent * Inability to perform physical tasks

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
Unidade Local de Saúde do Alto Alentejo (ULSAALE), Hospitals of Portalegre and Elvas, Portugal Portalegre Portugal

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 NCT06968273 on ClinicalTrials.gov ↗ ← All trials in Portugal