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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

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT00400270
Enrollment
56
Registered
2006-11-16
Start date
2004-10-31
Completion date
2006-01-31
Last updated
2015-05-28

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

Conditions

Asthma

Keywords

Asthma, Randomised controlled trial, Breathing exercises, Relaxation exercises, Primary care

Brief summary

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.

Interventions

PROCEDUREBreathing and relaxation exercises: the Papworth Method

Sponsors

Welwyn Hatfield Primary Care Trust
CollaboratorOTHER
University College, London
CollaboratorOTHER
University College London Hospitals
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Eligibility

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

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

Design outcomes

Primary

MeasureTime frame
Health related Quality of Life as measured by the St George's Respiratory Questionnaire

Secondary

MeasureTime frame
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.

Countries

United Kingdom

Outcome results

None listed

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