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Recruiting NCT06449573

Evaluation of Cardiopulmonary Parameters in Individuals With Asthma

— Observational Asthma

For patients and families

In plain language

An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.

What is being studied
The protocol lists: Exercise capacity.
Who it may be relevant to
Registry conditions: Asthma. Basic parameters: 18 years — 65 years · All.
What needs checking
Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
Where it takes place
Turkey (Türkiye)
Next step
Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →

Unsure about the terms? Read our patient guide →

Overview

The aim of the study compare the cardiopulmonary parameters of individuals with asthma with healthy subjects.

Detailed description

It is thought that aerobic capacity of asthmatic individuals decreases due to chronic respiratory disease, especially oxygen consumption. Detailed investigation will be provided with this research.

Interventions

  • Other Exercise capacity
    cardiopulmonary exercise test used assessment of exercise capacity

Primary outcome measures

  • Exercise capacity [Time frame: 20 minutes]
Secondary outcome measures (5)
  • Respiratory muscle strength [Time frame: 8 minutes]
  • Peripheral muscle strength [Time frame: 5 minutes]
  • Grip strength [Time frame: 3 minutes]
  • Kinesiophobia [Time frame: 3 minutes]
  • Quality of Life (symptoms, mood, activity limitation, environmental exposure) [Time frame: 10 minutes]

Eligibility criteria

Inclusion criteria

  • No respiratory, cardiovascular and metabolic diseases
  • Regular non-smoker

Exclusion criteria

  • Non-consenting
  • Pregnant women

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: Yes

Study design

Observational model
Case-control

Study locations

Turkey (Türkiye) · 1 center
  • Hacettepe University — Ankara

Identifiers

NCT: NCT06449573 · GO 23/533

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗