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Inspiratory Muscle Training in Pulmonary Hypertension

Inspiratory Muscle Training Effect on the Functional Capacity and the Quality of Life in Chronic Pulmonary Hypertension

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01410279
Enrollment
34
Registered
2011-08-05
Start date
2009-12-31
Completion date
2011-12-31
Last updated
2011-08-05

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

Conditions

Pulmonary Hypertension

Keywords

pulmonary hypertension, inspiratory muscle training, inspiratory muscle weakness, pulmonary functional, functional capacity, quality of life

Brief summary

The purpose of this study is evaluate the effect the inspiratory muscle training on the functional capacity of patients with pulmonary hypertension.

Detailed description

Pulmonary hypertension (PH) is a syndrome, in the case of hemodynamic alteration of a number of diseases and processes, such as the progressive increase in pulmonary vascular resistance, right heart failure and early death. Frequently patients with PH have reduced functional capacity, quality of life and survival. It was demonstrated recently that patients with HP also have inspiratory muscle weakness, possibly further increase the fatigue and dyspnea during exercise. To meet this need, inspiratory muscle training can lead to significant improvement in respiratory muscle strength, exercise tolerance and dyspnea, thus resulting in reduction of discomfort during activities of daily living, increase in exercise capacity and improved quality of life in different situations.

Interventions

OTHERInspiratory muscle training

The load is adjusted weekly in thirty percent of maximal inspiratory pressure of the subject.

Sponsors

Associação Fundo de Incentivo à Pesquisa
CollaboratorOTHER
Conselho Nacional de Desenvolvimento Científico e Tecnológico
CollaboratorOTHER_GOV
Hospital de Clinicas de Porto Alegre
Lead SponsorOTHER

Study design

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

Eligibility

Sex/Gender
ALL
Age
18 Years to 75 Years
Healthy volunteers
No

Inclusion criteria

* Clinical diagnosis pulmonary hypertension * World Health Organization (WHO) functional class II to IV * inspiratory muscle weakness

Exclusion criteria

* obesity * chronic obstructive pulmonary disease * orthopedic and neurological disease

Design outcomes

Primary

MeasureTime frame
The distance traveled in meters in the six minutes walk test after 8 weeks the inspiratory muscle trainingpatients will be monitored throughout the training protocol for 8 weeks

Secondary

MeasureTime frame
Increase in score of quality of life questionnaire after 8 weeks the inspiratory muscle trainingpatients will be monitored throughout the training protocol for 8 weeks

Countries

Brazil

Contacts

Primary ContactPedro Dal'Lago
pdallago@ufcspa.edu.br55(51)3303-8796
Backup ContactGlória M Ferreira
glomenz@yahoo.com.br55(51)9284.0703

Outcome results

None listed

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