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Efficacy of the Combination of Mindfulness and Buteyko Techniques for the Improvement of Poorly Controlled Asthma.

Efficacy of the Combination of General Relaxation (Mindfulness) and Respiratory (Buteyko) Techniques for the Improvement of Poorly Controlled Asthma. The MBA Study

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05593315
Enrollment
40
Registered
2022-10-25
Start date
2023-03-01
Completion date
2025-12-31
Last updated
2023-03-17

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

Conditions

Anxiety, Asthma, Stress

Keywords

Asthma, Anxiety, Stress, Mindfulness, Buteyko

Brief summary

Administration of a combined program for general (Mindfulness) and respiratory (Buteyko technique) relationship in patients with poorly controlled asthma and anxiety/stress to determine if it provides an improvement in current control and future risk of asthma.

Detailed description

A Mindfulness relaxation program and a Buteyko technique respiratory rehabilitation program will be administered individually and weekly, in 10 sessions (5 face-to-face and 5 telematic sessions afterwards). Patients will be visited 4 times (at inclusion, one month, 6 months and 12 months after the double intervention), where data on asthmatic morbidity, pulmonary function (spirometry), bronchial inflammation (FENO) will be collected and some questionnaires will be administered.

Interventions

OTHERMindfulness and Buteyko techniques

Joint implementation of a general relaxation program and a respiratory rehabilitation program in patients with poorly controlled asthma.

Sponsors

Fundació Institut de Recerca de l'Hospital de la Santa Creu i Sant Pau
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
OTHER
Masking
NONE

Intervention model description

A Mindfulness relaxation program and a Buteyko technique respiratory rehabilitation program will be administered individually and weekly, in 10 sessions (5 face-to-face and 5 telematic sessions afterwards).

Eligibility

Sex/Gender
ALL
Age
18 Years to 80 Years
Healthy volunteers
No

Inclusion criteria

* Diagnosis of poorly controlled asthma * In treatment with a combination of ICS/LABA at medium doses * Anxiety and/or functional dyspnea * Attended in the outpatient consultations of the Asthma Unit of the Pneumology and Allergy Service of the Hospital de la Santa Creu i Sant Pau in Barcelona

Exclusion criteria

* Severe asthma exacerbation in the last 30 days * Severe disabling comorbidity * Severe psychiatric illness * Inability to complete questionnaires.

Design outcomes

Primary

MeasureTime frameDescription
% patients with changed asthma control1 yearChanges in asthma symptoms measured with the asthma control test (minimum 5 as worse value; maximum 25, as the best value)
Changes in asthma exacerbation1 yearChanges in asthma exacerbation measured by number of hospital admissions and medical treatments received

Secondary

MeasureTime frameDescription
Pulmonary function1 yearChanges in pulmonary function with spirometry (Forced Expiratory Volume in 1 Second and forced vital capacity)
Anxiety1 yearImprovement of the anxiety level measured with the test hospital anxiety and depression scale (minimum 0 as the best value, maximum 42 as the worst value)
Therapeutic adherence of patients to inhalers1 yearChanges in therapeutic adherence of patients to inhalers with the Inhaler Adhesion Test
Bronchial inflammation1 yearChanges in bronchial inflammation with FENO
Functional dyspnea1 yearChanges in functional dyspnea measured with the test Nijmegen (minimum 0 as the worst value, maximum 64 as the worst value)

Countries

Spain

Contacts

Primary ContactVicente Plaza Moral, PhD
vplaza@santpau.cat+34 93 556 56 01

Outcome results

None listed

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