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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT04454242
Other study ID # 2020/09
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date June 1, 2021
Est. completion date June 1, 2022

Study information

Verified date January 2022
Source Ahi Evren Chest and Cardiovascular Surgery Education and Research Hospital
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The effect of expiratory muscle strength training (EMST) on sleep quality, disease severity, and respiratory muscle strength has been previously investigated in OSA syndrom. Only the effects of the high-intensity short-term EMST study in moderate OSAS patients were studied. High intensity and low intensity EMST has advantages and disadvantages.The study aims to compare the effects of high (60% MEP) and low (30% MEP) expiratory muscle strength training (EMST) on disease severity, sleep efficiency, snoring, fatigue severity and quality of life in severe OSAS patients.


Description:

Ahi Evren Chest Cardiovascular Surgery Training Research Hospital In sleep lab, polysomnography will be directed to the physiotherapist by the pulmonologist with severe OSAS patients. Patients will be divided into two groups by block randomization method. The study was planned as double-blind. Patients will not know what treatment they are receiving, the doctor does not know what treatment the patient is receiving, and technicians who take and analyze polysomnography will not know what treatment the patients are receiving. Severe OSAS patients with MEP 30% (low intensity) to the first group, MEP 60% (high intensity) to the second group with expiratory muscle training device, 7 days / week, 25 breaths per day, 1 minute rest for 5 breaths will be run with the cycle. The training will take a total of 8 weeks. The follow-up of the patients will be done remotely by phone. MEP measurements will be repeated every 2 weeks in the hospital and the new training workload will be calculated.


Recruitment information / eligibility

Status Completed
Enrollment 32
Est. completion date June 1, 2022
Est. primary completion date April 30, 2022
Accepts healthy volunteers No
Gender All
Age group 19 Years to 60 Years
Eligibility Inclusion Criteria: 1. Patients diagnosed with severe OSAS by Polysomnography in Ahi Evren Chest, Cardiovascular Surgery Training and Research Hospital Sleep Center will be included. 2. General health condition is stable Exclusion Criteria: 1. Passed stroke, 2. Neurological disease and psychological disease 3. Cardiac disease 4. Hypothyroidism 5. Serious obstructive nasal disease, 6. A history of infection in the past month. 7. Previous oroferengeal surgery history 8. With a BMI of 40 kg / m2 or more, 9. Using substance, alcohol, sedative and hypnotic drugs

Study Design


Intervention

Other:
Expiratory muscle trainig
This exercise will be used to strengthen forced expiratory muscles.

Locations

Country Name City State
Turkey Trabzon Ahi Evren Thoracic and Cardiovascular Surgery Training and Research Hospital Trabzon

Sponsors (2)

Lead Sponsor Collaborator
Ahi Evren Chest and Cardiovascular Surgery Education and Research Hospital The Scientific and Technological Research Council of Turkey

Country where clinical trial is conducted

Turkey, 

Outcome

Type Measure Description Time frame Safety issue
Other Antropometric measurements Neck circumference, Waist circumference, Hip circumference, Waist to hip ratio with circumference measurement method 2 day
Primary Disease severity Polysomnography recordings will be taken especially sleep efficiency and apnea-hypopnea index (AHI). Higher sleep efficiency and lower AHI values shows that patient have better status and lower disease severity 2 day
Primary Respiratory muscle strength Maximal inspiratory and expiratory muscle strength measurement with mouth pressure device 5 day
Secondary Daytime sleepiness Epworth Sleepiness Scale (ESS). Minimum and maximum scores: 0-24. The higher ESS score means the higher that person's average sleep propensity in daily life (ASP), or their 'daytime sleepiness' 2 day
Secondary Snoring severitiy and frequency Berlin Questionnaire: Snoring frequency (0-3) and severity (0-4). Higher scores show higher snoring frequency and severity. 2 day
Secondary Sleep quality The Pittsburgh Sleep Quality Index (PSQI). Minimum and maximum scores: 0-21. Higher PSQI scores show worse sleep quality. 2 day
Secondary Fatigue severity. Fatigue Severity Scale (FSS) . Minimum and maximum scores: 0-7. FSS scores higher than 4 shows high intensity fatigue perception 2 day
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