Breathing and Relaxation Exercises for Asthma: a Randomised Controlled Trial
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|ClinicalTrials.gov Identifier: NCT00400270|
Recruitment Status : Completed
First Posted : November 16, 2006
Last Update Posted : May 28, 2015
All patients on the GP asthma database in one practice were invited for an asthma physical-therapy assessment, at baseline. Volunteers satisfying the inclusion criteria ie - aged between 16 and 70, able to understand, read and write English, give informed consent, willing to attend the surgery to take part in the trial and with no other serious conditions - were invited to participate in the study. Patients were randomised either to a control group, receiving 2 more assessments at 6 and 12 months, or for comparison to a group receiving 5 physical-therapy treatments of integrated breathing and relaxation exercises (known as the Papworth Method (PM)). The two groups would then be compared at 6 and 12 months.
- The PM of breathing and relaxation training would improve the quality of life for adult patients with asthma in primary care, compared with patients only receiving usual medical care.
- Anxiety and depression, and symptoms from dysfunctional breathing would reduce compared with the control group.
- Respiratory function measurements would improve compared with the control group.
|Condition or disease||Intervention/treatment||Phase|
|Asthma||Procedure: Breathing and relaxation exercises: the Papworth Method||Not Applicable|
|Study Type :||Interventional (Clinical Trial)|
|Enrollment :||56 participants|
|Intervention Model:||Parallel Assignment|
|Masking:||None (Open Label)|
|Official Title:||A Physical Therapy Treatment for Adults Diagnosed With Asthma in Primary Care: a Randomised Controlled Trial|
|Study Start Date :||October 2004|
|Study Completion Date :||January 2006|
- Health related Quality of Life as measured by the St George's Respiratory Questionnaire
- Anxiety and Depression as measured by the Hospital Anxiety and Depression Scale.
- Symptoms from dysfunctional breathing measured by the Nijmegen Questionnaire.
- Respiratory measurements as measured by spirometry and capnography.
To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.
Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT00400270
|Bridge Cottage Surgery|
|Welwyn, Hertfordshire, United Kingdom, AL6 9EF|
|Study Director:||Professor Robert West, PhD||Department of Epidemiology and Public Health, University College London|