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Clinical Trials/NCT01554072
NCT01554072
Completed
Not Applicable

Home-based Pulmonary Rehabilitation in COPD

University of Nove de Julho1 site in 1 country30 target enrollmentJanuary 2012

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Chronic Obstructive Pulmonary Disease
Sponsor
University of Nove de Julho
Enrollment
30
Locations
1
Primary Endpoint
Change from baseline of functional capacity and quality of life after Home-based rehab
Status
Completed
Last Updated
12 years ago

Overview

Brief Summary

Pulmonary rehabilitation consists of a multidisciplinary program of care for patients with chronic respiratory disease, which currently encompasses numerous features and physical training methods aimed at maintaining stability clinic for people with Chronic Obstructive Pulmonary Disease (COPD), especially in patients who, even with optimized clinical treatment, continue their decline and symptomatic physical functions and 8 so that these social. goals are achieved the patient with COPD should integrate into a program of RP assiduous and with accompanying several times per week, for several months, which for a number of factors is not always possible. For this reason, it is the research of methodology of RP that hold their effectiveness, but with greater flexibility and viability to people with COPD. On this basis, this study aims to investigate the effectiveness of a program of RP semi-domiciliar in which the patient suffering from COPD can receive guidance and training in person, to develop it partially in own domicile.

Detailed Description

The protocol of the experimental procedure will begin with the explanation of the purpose, risks and benefits of the study volunteers to patients with COPD. Subsequently, based on an evaluation form, will collect data on the past history and current disease and performed a general physical examination. Then the patients will respond to two questionnaires. The first will research the Medical Council (MRC) 13, which is a dyspnea scale to categorize in terms of disability, patients with COPD. The second questionnaire will be the Airway Questionnaire 20 (AQ20) 14 specific for obstructive pulmonary disease, which is validated for the local language and highly reliable for the evaluation of patients with COPD, containing 20 questions related to respiratory health to evaluate the quality of life. Subsequently, the same day, the patients carry out the following tests: spirometry, respiratory muscle strength, respiratory muscle endurance, assessment of training load of the upper and shuttle test and bioimpedance

Registry
clinicaltrials.gov
Start Date
January 2012
End Date
December 2012
Last Updated
12 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Fernanda Dultra Dias

Principal Investigator

University of Nove de Julho

Eligibility Criteria

Inclusion Criteria

  • will be included patients of both sexes,
  • over 40 years and diagnosis of COPD according to criteria of ATS, GOLD and II Brazilian Consensus of COPD.
  • must be medically stable,
  • without having presented the framework of exacerbation of disease over the past 30 days and,
  • must have agreed to participate in this study which, after being presented and explained to patients, this accepted should be confirmed by Subscription Term of free and informed consent, pursuant to resolution 96 of 1996 of MS.

Exclusion Criteria

  • will be excluded from the study patients with serious comorbidity,
  • orthopedic diseases such as heart defects in upper and lower limbs,
  • sequelae of motor neurological disorders or impaired that may interfere with the ability to carry out physical exercise,
  • uncontrolled hypertension,
  • lung diseases and
  • those who do not grant support to participation in this study.

Outcomes

Primary Outcomes

Change from baseline of functional capacity and quality of life after Home-based rehab

Time Frame: After two months of treatment

Observe the effectiveness of home rehabilitation on functional capacity and quality of life among the placebo group and intervention as well as pre and post assessment patient care intervention group

Study Sites (1)

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