Breathing and Relaxation Exercises for Asthma: a Randomised Controlled Trial

This study has been completed.
Sponsor:
Collaborators:
Welwyn Hatfield Primary Care Trust
University College, London
Information provided by:
University College London Hospitals
ClinicalTrials.gov Identifier:
NCT00400270
First received: November 15, 2006
Last updated: November 20, 2006
Last verified: November 2006

November 15, 2006
November 20, 2006
October 2004
Not Provided
Health related Quality of Life as measured by the St George's Respiratory Questionnaire
Same as current
Complete list of historical versions of study NCT00400270 on ClinicalTrials.gov Archive Site
  • 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.
Same as current
Not Provided
Not Provided
 
Breathing and Relaxation Exercises for Asthma: a Randomised Controlled Trial
A Physical Therapy Treatment for Adults Diagnosed With Asthma in Primary Care: a Randomised Controlled Trial

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.

Hypotheses:

  1. 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.
  2. Anxiety and depression, and symptoms from dysfunctional breathing would reduce compared with the control group.
  3. Respiratory function measurements would improve compared with the control group.
Not Provided
Interventional
Not Provided
Allocation: Randomized
Endpoint Classification: Efficacy Study
Intervention Model: Parallel Assignment
Masking: Open Label
Primary Purpose: Treatment
Asthma
Procedure: Breathing and relaxation exercises: the Papworth Method
Not Provided
Not Provided

*   Includes publications given by the data provider as well as publications identified by ClinicalTrials.gov Identifier (NCT Number) in Medline.
 
Completed
56
January 2006
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Inclusion Criteria:

  • doctor diagnosed asthma, volunteers from the practice asthma database
  • 16-70 years of age
  • able to understand, speak and write English
  • willing to give informed consent
  • willing and able to attend the surgery for assessments and treatments

Exclusion Criteria:

  • serious co-morbid conditions
Both
16 Years to 70 Years
No
Contact information is only displayed when the study is recruiting subjects
United Kingdom
 
NCT00400270
EC03660
Not Provided
Not Provided
University College London Hospitals
  • Welwyn Hatfield Primary Care Trust
  • University College, London
Study Director: Professor Robert West, PhD Department of Epidemiology and Public Health, University College London
University College London Hospitals
November 2006

ICMJE     Data element required by the International Committee of Medical Journal Editors and the World Health Organization ICTRP