Clinical Trials Directory

Trials / Completed

CompletedNCT03729583

The Effects of Breathing Retraining in Patients With Interstitial Lung Diseases

The Effects of Breathing Retraining on Dyspnoea Measures and the Six-Minute Walking Distance in Patients With Interstitial Lung Diseases

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
30 (actual)
Sponsor
University of Malta · Academic / Other
Sex
All
Age
Healthy volunteers
Not accepted

Summary

Breathing retraining has been reported to lead to improvements in dyspnoea and walking distance in chronic obstructive pulmonary disease (COPD) patients. Evidence regarding the effects of such an intervention in ILD patients is though lacking. In view of this, the aims of such a study were to identify whether breathing retraining led to better management of dyspnoea and improved walking distance in ILD patients.

Detailed description

One of the commonest symptoms experienced in patients with a diagnosis of interstitial lung disease (ILD) is shortness of breath, a symptom which greatly affects their abilities to carry out activities of daily living. Breathing retraining has been reported to lead to improvements in dyspnoea and walking distance in chronic obstructive pulmonary disease (COPD) patients. Evidence regarding the effects of such an intervention in ILD patients is though lacking. In view of this, the aims of such a study were to identify whether breathing retraining led to better management of dyspnoea and improved walking distance in ILD patients. Twenty Seven ILD patients were randomly distributed to either the control group (n=15) which received a 12-week Pulmonary Rehabilitation (PR) programme without breathing retraining or the active group (n=12) which received a 12-week PR programme with breathing retraining. All patients had both the 6-minute walk test and their level of breathlessness assessed using the Dyspnoea Borg scale assessed at baseline and at 4 weekly intervals for a 12-week period throughout the programme.

Conditions

Interventions

TypeNameDescription
BEHAVIORALPulmonary RehabilitationA 12 week high intensity PR programme was delivered to both groups. The active group had additional breathing control interventions and exercises

Timeline

Start date
2017-07-01
Primary completion
2017-11-30
Completion
2018-05-18
First posted
2018-11-02
Last updated
2018-11-02

Locations

1 site across 1 country: Malta

Source: ClinicalTrials.gov record NCT03729583. Inclusion in this directory is not an endorsement.