Actively Recruiting

Phase Not Applicable
Age: 18Years +
All Genders
NCT06707623

CPET Guided Rehab vs Physiotherapy in Patients With Dysfunctional Breathing

Led by Evangelismos Hospital · Updated on 2026-04-14

78

Participants Needed

1

Research Sites

209 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

In this study the efficacy of a pulmonary rehabilitation program tailored to the needs of patients with dysfunctional breathing (DB) will be investigated using cardiopulmonary exercise testing. The pulmonary rehabilitation program will be compared with physiotherapy which is currently the mainstream therapy of DB.

CONDITIONS

Official Title

CPET Guided Rehab vs Physiotherapy in Patients With Dysfunctional Breathing

Who Can Participate

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Dysfunctional breathing (DB) diagnosed with CPET.
  • Adult patients (>18 years of age).
  • Able and willing to attend an outpatient multidisciplinary, supervised rehabilitation program lasting 8 weeks.
  • Able and willing to attend 5 physiotherapy sessions over 9 weeks.
  • Signed informed consent.
Not Eligible

You will not qualify if you...

  • No underlying pathology explaining dyspnea and DB in CPET (e.g. normal dead space to tidal volume ratio and normal alveolar-arterial gradient).
  • Patients with COPD.
  • Patients with uncontrolled asthma.
  • Patients with post-exertional malaise (PEM).
  • Patients unable to attend an outpatient rehabilitation program due to dementia, chronic paralysis, paraplegia, multiple injuries, serious orthopedic disability, end-stage cancer, neurological diseases requiring specialized rehabilitation clinics or interventions (e.g., speech therapy, kinesiotherapy).

AI-Screening

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Trial Site Locations

Total: 1 location

1

Pulmonary Rehabilitation Unit, 1st Department of Critical Care and Pulmonary Services Evangelismos Hospital

Athens, Attica, Greece, 10676

Actively Recruiting

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Research Team

A

Andreas Asimakos, MD, PhD

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

SINGLE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

TREATMENT

Number of Arms

2

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