Effect of Inspiratory Muscle Training

Sleep Apnea, Obstructive Clinical Trial

— MARITSA  

Official title:

Effect of Inspiratory Muscle Training in Sleep Apnea of Elderly

Clinical Trial Details — Status: Recruiting

Administrative data

• NCT number: NCT03190850
• Other study ID #: 150276
• Status: Recruiting
• Phase: N/A
• First received: March 23, 2017
• Last updated: June 15, 2017
• Start date: April 5, 2016
• Est. completion date: May 10, 2018

Study information

• Verified date: June 2017
• Source: Hospital de Clinicas de Porto Alegre
• Contact: Denis Martinez
• Email: dm[@]ufrgs.br
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

This study aims to evaluate the effect of inspiratory muscle training on sleep apnea in the elderly. The patients screened will be randomized and allocated into two groups, intervention and control. In the intervention group, the patients will perform the exercises with the inspiratory muscular training apparatus called Powerbreathe with progressive load, according to its inspiratory muscular force. The control group will perform the same exercises, with the same apparatus, but without load.

Description:

At the beginning of the study the patients will be evaluated initially with polysomnography. Patients who meet the inclusion criteria and sign the consent form will be evaluated with the following exams before and after inspiratory muscle training: manovacuometry, spirometry, diaphragmatic ultrasound and an anthropometric evaluation. After inspiratory muscle training, all patients will also perform polysomnography again to check for apnea-hypopnea index change.The patients screened will be randomized and allocated into two groups, intervention and control. In the intervention group, the patients will perform the exercises with the inspiratory muscular training apparatus called Powerbreathe with progressive load, according to its inspiratory muscular force. The control group will perform the same exercises, with the same apparatus, but without load.Patients in the intervention group will perform inspiratory muscle training as follows: in the first and second weeks, the patients will be instructed to perform the breathing exercises three times a week, performing four sets of six repetitions with one minute rest, with load of 50% of the maximum inspiratory pressure that will be preset in the Powerbreathe device by the study collaborators. At the end of the second week, they will perform reassessment of inspiratory pressures (MIP) and maximal expiratory pressure, with a 75% load adjustment of the PIM in the Powerbreathe device, and the patients being instructed to perform the same series and repetitions with frequency of exercise in five times in the week in the third and fourth week. At the end of the fourth week, they will perform a reassessment of the inspiratory pressures (MIP) and maximal expiratory pressures, with a 75% load adjustment of the MIP in the Powerbreathe device and the patients being instructed to perform the same series and repetitions with frequency of exercise in five times in the week on the fifth and sixth week. At the end of the sixth week, they will perform a reassessment of inspiratory pressures (MIP) and maximal expiratory pressure, with a 80% load adjustment of the MIP in the Powerbreathe device and the patients being instructed to perform the same series and repetitions with frequency of exercise in seven times in the week in the seventh and eighth week. The no-load (control) inspiratory muscle training group will perform the same series, repetitions and frequency of breathing exercises and reassessments of the intervention group, but there will be no load adjustment on the Powerbreathe appliances of this group.

Recruitment information / eligibility

• Status: Recruiting
• Enrollment: 30
• Est. completion date: May 10, 2018
• Est. primary completion date: March 9, 2018
• Accepts healthy volunteers: Accepts Healthy Volunteers
• Gender: All
• Age group: 65 Years to 80 Years

Eligibility

Inclusion Criteria:

• Age between 65 and 80 years

• Both genders

• Not be treating apnea with AHI between 10 and 30

• Do not tolerate or not have access to CPAP with any AHI

• To consent to participate in the research

Exclusion Criteria:

• Treatment for sleep apnea

• Severe chronic illness

• IAH greater than 35

• Uncontrolled arterial hypertension

• Acute myocardial infarction

• Recent upper airway trauma

• High performance athletes

• Medications with effect on the central nervous system

Related Conditions & MeSH terms

• Apnea
• Respiratory Aspiration
• Sleep Apnea Syndromes
• Sleep Apnea, Obstructive

Intervention

Other:
• Intervention
The device in which the breathing exercises will be performed will be adjusted with progressive loading aiming to improve muscular strength
• Control
The device in which the breathing exercises will be performed will not be adjusted with progressive loading.

Locations

Country	Name	City	State
Brazil	Hospital de Clinicas de Porto Alegre	Porto Alegre	Rio Grande do Sul

Sponsors (1)

Lead Sponsor	Collaborator
Hospital de Clinicas de Porto Alegre

Country where clinical trial is conducted

Brazil, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Effect of inspiratory exercise on apnea-hypopnea index in elderly patients with sleep apnea.	Impact of inspiratory muscle training on apnea-hypopnea index in elderly patients with sleep apnea. The measurement will be taken before and after the training. The measurement is apnea-hypopnea index through polysomnograph	8 weeks
Secondary	Effect of inspiratory training on maximal inspiratory and expiratory pressures	Impact of training muscle inspiratory on muscle strength inspiratory and expiratory measured through manovacuometry. The measurement will be taken before and after the training	8 weeks
Secondary	Effect of inspiratory muscle training on diaphragm thickness	Impact of training muscle inspiratory on diaphragm thickness measured through diaphragmatic ultrasound. The measurement will be taken before and after the training.	8 weeks