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GPIAG and Leicester Asthma and Dysfunctional Breathing (GLAD) Study: a Randomised Controlled Study

GPIAG and Leicester Asthma and Dysfunctional Breathing (GLAD) Study: a Randomised Controlled Study

Status
Completed
Phases
Phase 3
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT00515840
Acronym
GLAD
Enrollment
182
Registered
2007-08-14
Start date
2003-10-31
Completion date
2007-12-31
Last updated
2015-11-05

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Asthma, Respiratory

Brief summary

Breathing retraining supervised by a physiotherapist will result in improvements in the quality of life and asthma control of patients treated for asthma in the community with symptoms suggestive of dysfunctional breathing. To investigate the effects of breathing retraining on clinical and physiological parameters of asthma control, to identify the characteristics of patients who benefit, to perform a health economic evaluation.

Detailed description

Objectives: * To assess the effect of breathing retraining on asthma-related health status, asthma control and objective indices of asthma severity (bronchial hyper-reactivity (BHR), sputum eosinophilia and nitric oxide production) in patients with symptomatic asthma. * To compare the relationship between symptoms of dysfunctional breathing (Nijmegen Questionnaire screening score), changes in asthma-related health status and other parameters resulting from breathing retraining * To explore the relationship between dysfunctional breathing, baseline asthma symptoms, treatment and asthma-related quality of life. * To estimate the cost effectiveness of the breathing retraining intervention

Interventions

Physiotherapist administered breathing retraining programme

Sponsors

University Hospitals, Leicester
CollaboratorOTHER
P Burns
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
17 Years to 70 Years
Healthy volunteers
No

Inclusion criteria

* Asthma diagnosis in medical records * Age 17-70 yrs. * One or more prescription for asthma medication in previous 12 months * Impaired asthma related quality of life (AQLQ score \<5.5)

Exclusion criteria

* COPD * Unstable or under-treated asthma at enrollment.

Design outcomes

Primary

MeasureTime frame
Change in AQLQ scores between intervention and control groups in subjects with positive NQ screening scores 1 month post intervention Change in AQLQ scores between intervention groups of subjects with positive and negative NQ screening scoresDec 2006

Secondary

MeasureTime frame
Changes in bronchial hyperresponsiveness(PC 20), sputum eosinophil counts and exhaled NO between intervention and control groups in subjects with positive and negative NQ screening scores Change in ACQ Score between the intervention and the control grDec 2007

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026