Respiratory Muscle Stretching Effect on Functional and Electromyographic Parameters of Patients With and Without COPD

Universidade Federal do Pampa

Status: Unknown

Conditions: COPD

Treatments: Procedure: Sham; Procedure: PNF

Study type: Interventional

Funder types: Other

Identifiers

NCT03417908

09-411

Details and patient eligibility

About

To evaluate the activation of accessory respiratory muscles and the effects of stretching these muscles in patients with COPD.

Full description

All subjects (sixty men) will perform spirometry, measure of inspiratory capacity (IC) and maximal inspiratory and expiratory pressures (MIP and MEP). Baseline blood pressure (BP), respiratory rate (RR), heart rate (HR), sensation of dyspnea (Borg Scale) and oxygen saturation (pulse oximetry, SpO2) will be collected prior to the performance of pulmonary function tests.

The electrical activity of the scalene (ESC), sternocleidomastoid (SCM) and external intercostal muscles (INTER) will be measured by surface electromyography (sEMG) at rest and during the maneuvers of IC, MIP and MEP.

Control group: The control group will perform isotonic concentric contraction of the biceps (two sets of five push-ups elbow in both arms) with the individual sitting in a chair with back support.

Intervention group: The contract-relax method of proprioceptive neuromuscular facilitation (PNF) technique will be used for stretching of ESC, ECM and external intercostals muscles. The contraction of agonist muscles against the resistance imposed by the physiotherapist (isometric contraction) is maintained for 6 seconds. After that, the patient will be asked to relax the muscles for 6 seconds without losing range of motion, and then the muscle will be lengthened. This procedure is repeated until the maximum amplitude of motion of the neck and upper limb is reached. The stretching will be performed on the right and left sides of the body.

Statistical analysis will be carried out with the Statistical Package for the Social Sciences, version 18.0 (SPSS Inc., Chicago, IL, USA). Normality of data distribution will be assessed by the Shapiro-Wilk test.

Values will be presented as mean ± standard deviation (SD) or median (25-75%). To compare the differences between the baseline characteristics between the groups the t test for independent samples will be used. The effect of the intervention will be evaluated by paired t test. For the analysis of the electromyographic signal will be use the Wilcoxon T test. Statistical significance is accepted at p < 0.05.

Enrollment: 60 patients

Sex: Male

Ages: 40+ years old

Volunteers: Accepts Healthy Volunteers

Inclusion criteria

• Control group: Men without respiratory symptoms and lung disease, with normal spirometry.
• Interventional group: Men diagnosed with severe to very severe COPD (forced expiratory volume in one second / forced vital capacity - FEV1/FVC <0.7 and FEV1 <50% predicted after bronchodilator use); clinically stable over the past 4 weeks.

Exclusion criteria

• History of fracture in the spine and / or upper limb
• Herniated disc
• Connective tissue disease
• Ischemic heart disease or uncontrolled hypertension
• Obesity (BMI> 30 kg/m2)
• Aortic aneurysm
• Recent abdominal or thoracic surgery
• Glaucoma
• Retinal detachment

Trial design

Primary purpose: Treatment

Allocation: Randomized

Interventional model: Parallel Assignment

Masking: Single Blind

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60 participants in 4 patient groups

COPD - PNF

Active Comparator group

Description:

COPD - PNF

Treatment:

Procedure: PNF

COPD - sham

Sham Comparator group

Description:

COPD - sham

Treatment:

Procedure: Sham

Individuals Without COPD - PNF

Active Comparator group

Description:

Individuals Without COPD - PNF

Treatment:

Procedure: PNF

Individuals Without COPD - sham

Sham Comparator group

Description:

Individuals Without COPD - sham

Treatment:

Procedure: Sham