- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06467682
12-week Tele-exercise Program in Patients With OSA
The Role of a Wearables-track Tele-exercising Program on Cognitive Function and Brain Oxygenation in Patients With Obstructive Sleep Apnea
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
Background: Obstructive sleep apnea (OSA) is characterized by repetitive episodes of obstruction of the upper airway during sleep and leads to intermittent hypoxia, sleep fragmentation, hypercapnia and sympathetic hyperactivity which are associated with multiple adverse effects on health, in particular with brain health. Hyperarousability in OSA has a negative impact on sleep in the macro- and micro-architecture and sleep continuity, both of which are important players in neurogenesis, brain plasticity, alertness, and memory formation and consolidation. Thus, chronic sleep changes caused by OSA could negatively affect cognitive health. Both sleep fragmentation and intermittent hypoxia interfere with brain structure and function, increasing their vulnerability to neurodegenerative diseases. The prevalence of OSA is increasing as it is conjoined with obesity and it tends to elude clinicians' attention, as in only 10% of the population the definitive diagnosis can be established. Almost 80% of OSA patients report declining performance at work while 40% of dementia risk is attributable to modifiable risk factors such as physical inactivity.
Exercise offers a wide variety of benefits for the general population as it improves the cardiopulmonary, and metabolic profile. In addition, exercise is recommended as a low-cost, easily administered, and non-pharmacologic intervention, with positive effect on brain health and cognitive function, mainly by improving the sleep architecture, by enhancing the neurovascular oxygenation process and cerebral oxygenation, by reducing sympathetic overactivity and improving vascular function at rest and during exercise or mental stress. Finally, it has been shown that exercise can counteract the many aspects of decline in the brain's environment, such as the reduced blood flow and the lack of important factors (i.e. brain-derived neurotrophic factor-BDNF) that nurture brain neurons and encourage the growth and development of new neurons and synapses.
Therefore, long-term exercise providing the greatest and longest-lasting benefits e.g. increase cerebral neurovascular dynamics as assessed with functional Near-Infrared Spectroscopy (fNIRS) method and the intensity of exercise being related to cognitive functions such as improve memory after 12-week aerobic exercise and exercise with resistances. The effectiveness of different physical activity programs has not been properly established and some studies suggest that supervised versus self-selected programs might have similar results. In addition, the types of exercise programs in patients with sleep disorders have been addressed in literature. However, it has been noted that compliance in supervised programs in particular those lasting several weeks can often be an important limitation of the studies. Tele-exercising could be a key to overcome this important limitation, however, data on tele-exercising seems to be scarce.
Purpose: The main goal of the study is to explore the impact of a 12-week tele-exercising program on the cognitive profile as well as on specific parameters of brain functions, brain metabolism and brain oxygenation in patients with obstructive sleep apnea, thus highlighting the multidimensional relationship between physical exercise, cognition and brain oxygenation/metabolism. We will therefore apply a 12-week, wearable-track, tele-exercise intervention in patients with a Sleep Apnea Syndrome with and without cognitive impairment and compare the groups outcome on cognition and brain metabolism.
The primary aim of this study is to investigate the extent to which tele-exercise improves cognitive functions in patients with OSA.
For this aim, we will compare the cognitive performance at baseline and at 12-weeks follow-up in 3 groups of patients.
- Patients with OSA without cognitive impairment
- Patients with cognitive impairment assigned to a 12-week tele-exercising program
- Patients with cognitive impairment not assigned to a tele-exercising intervention
For the screening of cognitive impairment and the evaluation of cognitive outcome, the following cognitive tests will be performed:
- Attention/orientation, memory, verbal fluency, language and visuospatial abilities at ADDENBROOKE'S COGNITIVE EXAMINATION - ACE-R.
- Outcome: Changes between baseline and follow-up at ACE-R subdomains' scores
- Executive function and rote memory
- Outcome: Score at Trail Making Test A and B (TMT)
- Verbal episodic memory based on subdomains of encoding process and immediate recall, free and cued recall, recognition and delayed recall
- Outcome: Score in a serial verbal learning task, with control of encoding and recall, according to the modified procedure of Grober and Buschke
- Procedural memory:
- Outcome: performance in a variation of the visual-motor skill-learning task the Mirror Tracing Task (MTT)
- Working memory with subdomains the auditory information processing speed, flexibility and working memory span:
- Outcome: performance in the Modified Paced Auditory Serial Addition Test (PASAT) and in a task for "Transformed Auditory Span".
The secondary aims of this study are:
To investigate the extent to which tele-exercise has a positive impact on brain oxygenation and metabolism in patients with OSA.
Outcome: cerebral oxygenation according to fNIRS-based measure levels of oxy-hemoglobin (HbO) and deoxygenated-hemoglobin (deoxy-Hb) For this aim, we will compare cerebral oxygenation values fNIRS- at baseline and following a 12-week follow-up in the, above mentioned, three groups of patients.
- Investigate the extent to which tele-exercise has a positive impact on sleep architecture in patients with OSA.
For this aim, we will compare polysomnography quantitative and qualitative parameters as well as scores in sleep/wake questionnaires at baseline and at 12 weeks follow-up in the, above mentioned, three groups of patients.
Outcomes: Change in sleep architecture, sleep staging features and respiratory features in PSG between baseline and 12-weeks follow up.
Participants: We will recruit patients with clinical suspicion of OSA from Sleep Outpatient clinics at the Nicosia General Hospital, Cyprus, to undergo in home-based polysomnography study with portable device [1]. We will perform a screening cognitive test (ACE-R) to identify individuals with cognitive impairment. Patients with OSA and cognitive impairment (CI) will be randomized to two groups: with CI that will undergo the tele-exercise program (TEp) (Group A, N=20) and with CI That will not undergo the TEp (Group B, N=20). A third matched group (Group C) of OSA patients without cognitive impairment (N=20) will act as another control group and will undergo the tele-exercise program. A sample size estimation, based on previous studies showed that 20 patients per group would be sufficient to detect differences in our primary outcome. Groups A and C will carry out a tele-exercise program form Unique Safe Tele-Exercise Project platform (https://ustep.gr), on a 12-week duration. All patients which will be enrolled in our study will receive non-CPAP treatment (delayed therapy). Α feasibility study will precede with 10 OSA patients (Apnea-Hypopnea-Index, AHI >15 events/h) and similar characteristics, for a 12-week period of tele-exercising so as to investigate and record data related to exercise adherence, drop-out and compliance. All patients group they will be recommendations for diet focused on body weight loss as percent of body fat (where required) and sleep position to improve their quality of life (scale score).
Data collected: Study-related assessments include: a) standard lung function testing, followed by the diffusing capacity of the lungs for carbon monoxide according to ATS/ERS guidelines, b) physical fitness tests [6-MWT (meters) , handgrip strength test (kg) and 30s Sit-to-Stand (repetitions)], so as to record and assess O2 consumption (mL/min/kg) and muscle strength (kg), c) the perceptual ability and reaction time test (ms), d) prior to physical fitness tests, will answer questionnaires on: quality and patterns of sleep (PSQI), shifting attention and for selective attention (TMT A and Β), Epworth Sleep Scale (ESS), Karolinska Sleepiness Scale (KSS), cognitive impairment OSA risk (MoCA), and work ability (WAI) (scales scores) and e) assessments to record cerebral oxygenation-oxygenated (μmol/L) and deoxygenated hemoglobin (μmol/L) (fNIRS) during physical fitness tests, reaction time and when answering the questionnaires. All the above assessments will be performed at baseline and at follow-up in 3 months.
Interventions program: The 12-week TEp will be performed and supported by the uStep platform, with each patient taking part in 3 training sessions per week with a 60-min duration period per training session. There will be personalized training sessions: a) warm-up and warm-down (5-min respectively) with the mobility exercises and respiratory exercises for upper and lower limbs, b) aerobic exercise (30-min) with continuous outdoor walking (intensity calculation according HRpeak during 6MWT and self-reported feeling of dyspnea and leg fatigue) and c) multi-joint strength exercises (20-min) to improve the strength of upper and lower limbs (intensity calculation according to muscle strength tests). Participants of the tele-exercise program will use wearable-based tracking, during intervention period, to assessment the cardio-oxygenation.
Study Type
Enrollment (Estimated)
Phase
- Not Applicable
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Adult
- Older Adult
Accepts Healthy Volunteers
Description
Inclusion criteria
- age ≥18-to-≤70 years,
- apnea hypopnea index (AHI) ≥15 events/h,
- no contraindications (e.g. unstable angina during the previous month, myocardial infarction during the previous month, resting heart rate >120 bpm, systolic blood pressure >180 mmHg and diastolic blood pressure >100 mmHg) for 6-minute walk test (6MWT)
- body mass index (BMI) <40 kg/m2
- without daily physical working strain
- without active self-reported symptoms (fatigue and dyspnea)
- without pregnancy for women
- patients with preexistent musculoskeletal disability will be excluded since their condition might impair maximum exercise capacity
- all participants should speak and read Greek
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Basic Science
- Allocation: N/A
- Interventional Model: Single Group Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Other: 12-week intervention tele-exercise program
tele-exercise and tele-rehabilitation
|
The 12-week tele-exercise program will be performed and supported via the USTEP digital platform, with each patient taking part in 3 training sessions per week with a 60-min duration period per training session.
There will be personalized training sessions: i) warm-up and warm-down, ii) aerobic exercise, and iii) strength exercises.
All tele-exercise program participants, will use wearable-based tracking to assessment the cardio-oxygenation.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
The primary aim of this study is to investigate the extent to which tele-exercise improves cognitive functions in patients with OSA
Time Frame: Baseline and after 12-week
|
Absolute number (scale score) in both the total score and the domains of the MoCA questionnaire (assessing cognitive impairment), individual patient, between baseline and after 12 weeks of intervention.
|
Baseline and after 12-week
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
To investigate the extent to which tele-exercise has a positive impact on brain oxygenation in patients with OSA.
Time Frame: Baseline and after 12-week
|
Absolute number (μmol/L) in brain oxygenation (fNIRS method), individual of patient, between baseline and after 12 weeks of intervention.
|
Baseline and after 12-week
|
|
To investigate the extent to which tele-exercise has a positive impact on brain metabolism in patients with OSA.
Time Frame: Baseline and after 12-week
|
Absolute number (μmol/L) in brain metabolism (fNIRS method), individual of patient, between baseline and after 12 weeks of intervention.
|
Baseline and after 12-week
|
|
Investigate the extent to which tele-exercise has a positive impact on sleep architecture in patients with OSA.
Time Frame: Baseline and after 12-week
|
Percentage change for each sleep stage (REM and non-REM), individual of patient, between baseline and after 12 weeks of intervention.
|
Baseline and after 12-week
|
|
To investigate to what extent tele-exercise has a positive effect on oxygen saturation during sleep in patients with OSA.
Time Frame: Baseline and after 12-week
|
Duration (min) of in-nadir oxygen saturation during sleep, individual of patient, between baseline and after 12 weeks of intervention.
|
Baseline and after 12-week
|
|
To investigate the extent to which tele-exercise has a positive impact on Apnea Hypopnea Index in patients with OSA.
Time Frame: Baseline and after 12-week
|
Absolute number of Apnea Hypopnea Index (events/h), individual of patient, between baseline and after 12 weeks of intervention.
|
Baseline and after 12-week
|
Collaborators and Investigators
Sponsor
Study record dates
Study Major Dates
Study Start (Estimated)
Primary Completion (Estimated)
Study Completion (Estimated)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- EEBK/EP 2023/60
- 101034403 (Other Grant/Funding Number: ONISILOS - University of Cyprus - Marie Skłodowska-Curie)
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
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