Clinical trial Recruiting at 1 site Interventional

Combined endurance training for improving daily activities in COPD patients

Official title: Effect of Combined Upper and Lower Extremity Endurance Training Versus Lower Extremity Training Alone on ADL and Walking in COPD Patients

Run by Istituti Clinici Scientifici Maugeri SpA · NCT05708443 · Data updated 2026-11-12

This study is testing if combined upper and lower body endurance training can help people with COPD do daily activities better and walk more easily.

Quick facts

Study typeInterventional
SexAll
Enrollment36 (estimated)
SponsorIstituti Clinici Scientifici Maugeri SpA
Academic / other
Locations3 sites (Lumezzane, Brescia and 2 other locations)
StatusRecruiting
StartedJanuary 10, 2023
Main results expectedFebruary 28, 2027
Study endsJune 30, 2027
Registry record updatedJune 24, 2026
Trial IDNCT05708443 on ClinicalTrials.gov

Is this trial a fit for you?

Likely a good fit

Ideal candidates for this study are individuals diagnosed with GOLD class 2-3 COPD who can walk and climb stairs independently.

Probably not a fit

Patients with severe comorbidities, cognitive impairments, or those requiring long-term oxygen therapy may not benefit from this study.

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

This study evaluates the effects of combined upper and lower limb endurance training on activities of daily living (ADL) and walking ability in patients with Chronic Obstructive Pulmonary Disease (COPD). The intervention includes pulmonary rehabilitation that focuses on enhancing exercise tolerance and reducing symptoms such as dyspnea and fatigue. Participants will be divided into groups receiving either lower limb training or combined upper and lower limb training to assess the additional benefits of the latter. The study aims to improve the quality of life and functional capacity of COPD patients through structured exercise regimens.

Why it matters

Potential benefit: If successful, this approach could significantly enhance the ability of COPD patients to perform daily activities and improve their overall quality of life.

How similar studies have gone: Previous studies have shown positive outcomes with similar rehabilitation approaches, indicating potential for success in this study.

Who can join: the full rules

Show full inclusion / exclusion criteria
Inclusion Criteria:

* GOLD class 2-3 COPD
* Forced Expiratory Volume in the first second (FEV1) between 30% and 70% of the predicted value
* ability to walk and climb stairs without assistance
* stable clinical condition (pH \> 7.35)

Exclusion Criteria:

* chronic respiratory insufficiency on long-term oxygen therapy (LTOT)
* severe orthopedic, neurological or cardiological comorbidities
* cognitive impairment
* recent exacerbation (within 15 days) requiring a change in therapy
* presence of lung disease other than COPD
* terminality

Where it's running

  • ICS Maugeri IRCCS, Respiratory rehabilitation of the Institute of Lumezzane
    Lumezzane, Brescia, Italy
    Recruiting
  • ICS Maugeri IRCCS, Respiratory rehabilitation of the Institute of Montescano
    Montescano, Pavia, Italy
    Not yet recruiting
  • ICS Maugeri IRCCS, Respiratory rehabilitation of the Institute of Tradate
    Tradate, Varese, Italy
    Completed

Study contacts

Similar studies

Other studies for the same condition or treatment. Recruiting studies are listed first.

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  • Balance training after pulmonary rehab for COPD to help steadiness and reduce falls

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  • Continuous vs High-Intensity Interval Exercise in COPD

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  • HRS-9821 Inhalation Suspension for COPD: Safety and Dose Finding in Adults

    This study tests whether HRS-9821 inhalation can be safely taken and help people with moderate to severe COPD, and aims to find a reasonable dose.

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How to take part

  1. Review the eligibility criteria above with your treating physician.
  2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
  3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.
Last reviewed 2026-11-14 by the Find a Trial editorial team. Information on this page is for educational purposes and is not medical advice. Always consult qualified healthcare professionals about clinical trial participation.