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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT03080662
Other study ID # INAF
Secondary ID
Status Recruiting
Phase N/A
First received March 7, 2017
Last updated March 14, 2017
Start date January 22, 2015
Est. completion date March 15, 2018

Study information

Verified date March 2017
Source Parc de Salut Mar
Contact Diego Agustin Rodriguez, PhD
Phone 0034932483548
Email DARodriguez@parcdesalutmar.cat
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The impact of the reduction of daily physical activity (DPA) in patients with COPD (chronic obstructive pulmonary disease) is a highly studied area, due to its impact on the quality of life and the clinical evolution of the disease . This fact has multifactorial components: its function is naturally diminished with time, and its effects on the loss of physical condition (decondition). However, dynamic hyperinflation and respiratory muscular dysfunction, especially in patients with more symptomatology, have been identified as those that have the most relevant factors that impact on daily physical activity Due to the detrimental effects of the pulmonary hyperinflation, the diaphragm is flatter and shorter, being in a position of mechanical disadvantage. This contributes to a reduced effort capacity and increase in the dyspnea of patients during daily activities.

Resistance training improves their exercise capacity and reduces dyspnea, however it does not improve inspiratory muscle strength. It is for this reason, that specific training of the inspiratory muscles, offers special interest in patients with decreased inspiratory muscle strength and pulmonary hyperinflation.


Recruitment information / eligibility

Status Recruiting
Enrollment 20
Est. completion date March 15, 2018
Est. primary completion date December 15, 2017
Accepts healthy volunteers No
Gender All
Age group 45 Years to 80 Years
Eligibility Inclusion Criteria:

- To be eligible for the respiratory rehabilitation programme participants must have stable COPD (at least 4 weeks), inspiratory muscle weakness (PImax <70%) and pulmonary hyperinflation (TLC > 120%). Patient that have signed inform consent.

Exclusion Criteria:

- Hospitalization within the previous 14 days

- Current participation in rehabilitation program,

- Locomotor or neurological condition or disability limiting the ability to perform exercise,

- Lung transplantation or lung volume reduction surgery foreseen within 1 month after discharge.

Study Design


Related Conditions & MeSH terms


Intervention

Device:
ORYGEN DUAL Sham Valve
Training of the inspiratory muscles during 5 weeks
ORYGEN DUAL Valve
Training of the inspiratory muscles during 5 weeks

Locations

Country Name City State
Spain Hospital Del Mar Barcelona

Sponsors (1)

Lead Sponsor Collaborator
Parc de Salut Mar

Country where clinical trial is conducted

Spain, 

Outcome

Type Measure Description Time frame Safety issue
Primary improvement of daily physical activity Change From Baseline at least 10% moderate to vigorous daily physical activity measured by accelerometer Baseline and 5 weeks
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