ClinicalTrials.Veeva

Menu

Helmet Ventilation During Self-Paced Walking Test

F

Fu Jen Catholic University

Status

Completed

Conditions

COPD

Treatments

Device: Helmet vetilation

Study type

Interventional

Funder types

Other

Identifiers

NCT04156724
C108032

Details and patient eligibility

About

The aim of this study is to investigate the use helmet ventilation (HV) in walking test and analysis of effect patients with COPD.

Full description

Chronic obstructive pulmonary disease (COPD) is characterized by persistent airflow limitation with chronic inflammation of the respiratory system. Symptoms of COPD may contribute to activity restriction, deconditioning and exercise intolerance. Non-invasive positive pressure ventilation (NIPPV) has been shown to improve exercise intolerance and health-related quality of life in patients with severe COPD. Helmet ventilation (HV) is a new option for NIPPV to alternative to nasal or face mask. A study which published on JAMA demonstrated the feasibility and benefits of HV. The aim of this study is to investigate the use helmet ventilation (HV) in walking test and analysis of effect patients with COPD.

Enrollment

20 patients

Sex

All

Ages

20+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Patents with COPD who confirm by pulmonary function test

Exclusion criteria

  • COPD AE within 3 months
  • Diagnosed neuromuscular disease
  • Unable to perform 6-MWT

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Crossover Assignment

Masking

Single Blind

20 participants in 2 patient groups

HV
Experimental group
Description:
6MWT with helmet ventilation
Treatment:
Device: Helmet vetilation
Control
No Intervention group
Description:
6MWT alone according to ATS guideline

Trial contacts and locations

1

Loading...

Data sourced from clinicaltrials.gov

Clinical trials

Find clinical trialsTrials by location
© Copyright 2026 Veeva Systems