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Effect of Inspiratory Muscle Training

Effect of Inspiratory Muscle Training in Sleep Apnea of Elderly

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03190850
Acronym
MARITSA
Enrollment
30
Registered
2017-06-19
Start date
2016-04-05
Completion date
2018-05-10
Last updated
2017-06-19

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Sleep Apnea, Obstructive

Keywords

Sleep Apnea, Elderly, Inspiratory training

Brief 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.

Detailed 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.

Interventions

OTHERIntervention

The device in which the breathing exercises will be performed will be adjusted with progressive loading aiming to improve muscular strength

OTHERControl

The device in which the breathing exercises will be performed will not be adjusted with progressive loading.

Sponsors

Hospital de Clinicas de Porto Alegre
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Investigator)

Masking description

The investigator will not know the final result of the tests performed until the end of the study

Eligibility

Sex/Gender
ALL
Age
65 Years to 80 Years
Healthy volunteers
Yes

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

Design outcomes

Primary

MeasureTime frameDescription
Effect of inspiratory exercise on apnea-hypopnea index in elderly patients with sleep apnea.8 weeksImpact 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

Secondary

MeasureTime frameDescription
Effect of inspiratory training on maximal inspiratory and expiratory pressures8 weeksImpact of training muscle inspiratory on muscle strength inspiratory and expiratory measured through manovacuometry. The measurement will be taken before and after the training
Effect of inspiratory muscle training on diaphragm thickness8 weeksImpact of training muscle inspiratory on diaphragm thickness measured through diaphragmatic ultrasound. The measurement will be taken before and after the training.

Countries

Brazil

Contacts

Primary ContactDenis Martinez
dm@ufrgs.br

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026