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Free Walking Exercise in Obstructive Sleep Apnea Patients With Non-alcoholic Fatty Liver

Impact of Free Walking Exercise on Obstructive Sleep Apnea Patients With Non-alcoholic Fatty Liver on Liver Enzymes, Degree of Exhaustion, and Quality of Sleep

Status
Recruiting
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06508190
Enrollment
40
Registered
2024-07-18
Start date
2024-07-12
Completion date
2024-12-01
Last updated
2024-07-18

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

Conditions

Non-alcoholic Fatty Liver, Obstructive Sleep Apnea

Brief summary

Research evaluating the impact of continuous positive airway pressure (CPAP) & walking exercise on fatigue severity, liver enzymes and sleeping quality in patients with non-alcoholic fatty liver disease who also have obstructive sleep apnea. Forty patients are divided into two groups: twenty patients CPAP and other twenty patients for CPAP and walking program .

Detailed description

Research evaluating the impact of continuous positive airway pressure (CPAP) & walking exercise on fatigue severity, liver enzymes and sleeping quality in patients with non-alcoholic fatty liver disease who also have obstructive sleep apnea. Forty patients are divided into two groups: twenty patients CPAP and other twenty patients for CPAP and walking program .

Interventions

BEHAVIORALcontinuous positive airway pressure

continuous positive airway pressure therapy for a period of 12 weeks, all patients with in this group are required to utilize the CPAP machine for at least 4 hours each night

BEHAVIORALfree walking exercise and continuous positive airway pressure

patients will receive continuous positive airway pressure therapy for a period of 12 weeks, all patients with in this group are required to utilize the CPAP machine for at least 4 hours each night. Also, patients will perform walking exercise for 30 mint, daily for 12 weeks

Sponsors

Ahram Canadian University
Lead SponsorOTHER

Study design

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

Masking description

The authors of this clinical trial and patients do not provide the study outcome examiners with information regarding device therapy or free walking exercise.

Intervention model description

Forty patients suffering from obstructive sleep apnea are divided into two groups: one for CPAP and the other for CPAP and free walking program.

Eligibility

Sex/Gender
ALL
Age
40 Years to 65 Years
Healthy volunteers
No

Inclusion criteria

* The body mass index (BMI) \< 35 kg/m2. * obstructive sleep apnea patients with fatty liver

Exclusion criteria

* liver transplantation , alcoholic fatty liver, antipsychotic medications, bariatric surgery; cardiac , renal problem , liver cancer ; pregnancy,orthopedic problems, systemic diseases, respiratory dysfunctions, neurological dysfunctions.

Design outcomes

Primary

MeasureTime frameDescription
Alanine tranaminaseit will be measured after 12 weeksserum hepatic enzyme

Secondary

MeasureTime frameDescription
Body mass indexit will be measured after 12 weeksit will be masusured on empty stomach and bladder
triglycerodesit will be assessed after 12 weeksit will be meausred in plasma
Asparatate transamianseit will be measured after 12 weeksserum hepatic enzyme
fatigue severity scaleit will be assessed after 12 weeksa questionnaire that wil be used for assessing fatigue
Epworth sleepness scaleit will be assessed after 12 weeksa questionnaire that wil be used for daytime sleepness
Pittsiburg sleeping quality indexit will be assessed after 12 weeksa questionnaire that wil be used for assessing sleeping quality

Countries

Egypt

Contacts

Backup ContactEl-gohary Ola, PHD
01227191398
Primary ContactEl-Hadidy Hagar, PHD
hagarhadidy2016@gmail.com00201007453552

Outcome results

None listed

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