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Clinical Trials/NCT02383277
NCT02383277UnknownNot Applicable

Acute Effects of a Stretching Program of the Rib Cage Muscles on the Regional Distribution of Ventilation and the Diaphragmatic Mobility of Patients With COPD During Exercise: a Randomized Crossover Clinical Trial

Universidade Federal de Pernambuco0 sites20 target enrollmentStarted: November 1, 2014Last updated:
Conditions
Interventions

Trial Snapshot

Phase
Not Applicable
Enrollment
20
Primary Endpoint
Endurance tolerance as measured by the duration of the exercise

Study Overview

Brief Summary

Investigate the effects of stretching the muscles of the rib cage in individuals with COPD during exercise.

Detailed Description

To investigate the effects of a stretching program for the muscles of the rib cage or control in patients with COPD during exercise and / or the immediate post-exercise, using the following parameters:

  • Tidal volume (VT), respiratory rate (RR), minute volume (MV), inspiratory time (Tins) and expiratory (T exp).
  • Change in volumes of total and regional chest magazines (pulmonary rib cage, abdominal rib cage and abdomen).
  • Diaphragmatic mobility.
  • electrical muscle activity
  • endurance time.
  • Dyspnea sensation.

Study Design

Study Type
Interventional
Allocation
Randomized
Intervention Model
Crossover
Primary Purpose
Treatment
Masking
Double (Participant, Investigator)

Eligibility Criteria

Ages
50 Years to 80 Years (Adult, Older Adult)
Sex
All
Accepts Healthy Volunteers
No

Inclusion Criteria

  • •Smoking history, occupational or environmental exposure to pollutants and / or symptoms of cough, dyspnea or hypersecretion;
  • •FEV1 <80% predicted and post-bronchodilator FEV1 / FVC <70% to confirm the diagnosis of airway obstruction not fully reversible bronchodilator therapy;
  • •Absence of co-morbidities that does not allow the realization of stress (hypertension, severe pulmonary hypertension, myocardial infarction, congestive heart failure, severe dyspnoea);
  • •Preserved cognitive functioning;
  • •Sedentary
  • •Clinically stable during the study period.

Exclusion Criteria

  • •Patients with cognitive, hearing or visual deficit;
  • •Changes in the neuro-musculo-skeletal system which endangers or impairs the assessment;
  • •Not be able to achieve at least three stages of the incremental test.

Arms & Interventions

Stretching and Exercise

Experimental

This group undergo a session of stretching aiming flexibility of the rib cage and later at an exercise test with constant load up to the limit of tolerance for exercise bike

Intervention: Stretching (Other)

Stretching and Exercise

Experimental

This group undergo a session of stretching aiming flexibility of the rib cage and later at an exercise test with constant load up to the limit of tolerance for exercise bike

Intervention: Exercise (Other)

Control and Exercise

Sham Comparator

This group will carry out the exercise test with constant load up to the limit of tolerance for exercise bike after a period of rest under the same environmental conditions and the experimental group time. During this time the therapist will place their hands but not performing the stretch.

Intervention: Control (Other)

Control and Exercise

Sham Comparator

This group will carry out the exercise test with constant load up to the limit of tolerance for exercise bike after a period of rest under the same environmental conditions and the experimental group time. During this time the therapist will place their hands but not performing the stretch.

Intervention: Exercise (Other)

Outcomes

Primary Outcomes

Endurance tolerance as measured by the duration of the exercise

Time Frame: Participants will be followed for the duration of the exercise, an expected average of 10 minutes

Dyspnea as measured by Borg Escale

Time Frame: Participants will be followed for the duration of the exercise, an expected average of 10 minutes

Secondary Outcomes

  • Diaphragm mobility measured by ultrasound(Participants will be followed for the duration of the stretching and the exercise, an expected average of 60 minutes)
  • Volumes of the chest wall measured by pletismography optoelectronic(Participants will be followed for the duration of the stretching and the exercise, an expected average of 60 minutes)
  • Muscle electrical activity measured by surface electromyography(Participants will be followed for the duration of the stretching and the exercise, an expected average of 60 minutes)

Investigators

Sponsor Class
Other
Responsible Party
Principal Investigator
Principal Investigator

Adriane Borba Cardim

Degree in Physical Therapy

Universidade Federal de Pernambuco

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