Analysis of Muscle Oxygen Saturation and Functional Variables During Physical Capacity Assessments in Patients With COPD

Trial statusNot yet recruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18+
SponsorUniversity of Extremadura

About this trial

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 criteria

This trial does not accept healthy volunteers

Qualifiers

Age ≥18 years

Clinical diagnosis of COPD

Medically cleared for physical exercise

Disqualifiers

Decompensated heart failure or exercise-limiting comorbidities

Cognitive impairment or legal incapacity to consent

Inability to perform physical tasks

Trial design

Design model

Single group

Treatments tested in this trial

  • Combined respiratory physiotherapy and cardiovascular-strength training program

    Behavioral

    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).

Treatment groups

15 Participants
are divided into 1 treatment group
Group A: Intervention GroupExperimental treatment 1 intervention

Trial outcomes

Primary outcomes

1

Change in muscle oxygen saturation (%)

Measured in intercostal, quadriceps, and triceps surae muscles using NIRS (Moxy Monitor) during 6MWT and 30CST, before and after the 4-week intervention.

Time frame
From baseline to end of intervention (4 weeks)

Secondary outcomes

1

Distance covered in 6-Minute Walk Test (6MWT)

Time frame
From baseline to after the 4-week intervention
2

Number of repetitions in the 30-Second Chair Stand Test

Time frame
From baseline to after the 4-week intervention
3

Perceived dyspnea and lower limb fatigue (Borg Scale)

Time frame
From baseline to after the 4-week intervention
4

Maximal inspiratory and expiratory pressures (Pimax and Pemax)

Time frame
From baseline to after the 4-week intervention

Other outcomes

Sponsors and contacts

Click on the lead sponsor to view all of their trials.

This trial is not recruiting at the moment. You can still explore other options: