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Inspiratory Muscle Training in Pulmonary Hypertension

I

Istanbul University

Status

Completed

Conditions

Pulmonary Hypertension

Treatments

Other: inspiratory muscle training

Study type

Interventional

Funder types

Other

Identifiers

NCT03385733
GAslan
BuketA (Other Identifier)

Details and patient eligibility

About

The aim of this study is to investigate the effective of inspiratory muscle training on respiratory function, exercise capacity, physical activity and quality of life.

Full description

Pulmonary hypertension (PH) is a condition which is seen with hemodynamic differences, pulmonary vascular resistance and right heart failure. Patients with pulmonary hypertension have, dyspnea, physical inactivity, reduced condition and respiratory muscle dysfunction. Aerobic exercise programs in patients with pulmonary hypertension are reported to result in improved exercise capacity and endurance of the patients, improvement in WHO functional class and quality of life, increased peak workload and increased peripheral muscle function. In recent years, few studies have investigated the efficacy of inspiratory muscle training in patients with PH.The aim of this study is to investigate the effective of inspiratory muscle training on respiratory function, exercise capacity, physical activity and quality of life.

Enrollment

30 patients

Sex

All

Ages

18 to 80 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Diagnosis of Pulmonary Hypertension,
  • NYHA functional class I-IV
  • MIP pressure <80 cm h2O

Exclusion criteria

  • COPD
  • Conditions which can limit the assessments
  • Insufficient cooperation

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Double Blind

30 participants in 2 patient groups

Inspiratory muscle training group
Experimental group
Description:
Patients will continue 8 weeks, 5 days, 2 times 15 minutes training program with %30 MIP at home.
Treatment:
Other: inspiratory muscle training
control group
No Intervention group
Description:
Patients will continue 8 weeks, 5 days, 2 times 15 minutes training program with 9 cmH2O pressure at home.

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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