Gamified workouts before bed may ease sleep apnea
NCT ID NCT07214636
First seen Jun 27, 2026 · Last updated Jul 29, 2026 · Updated 2 times
Summary
This study tests a digital, game-like exercise system called ApneaTheraPlay for people with obstructive sleep apnea. Participants will do a mix of breathing, aerobic, strengthening, and throat exercises three times a week for 12 weeks, either through the game or a structured program. The goal is to see if these pre-sleep workouts can reduce apnea events and improve oxygen levels. The trial involves 54 adults aged 18–65 with mild to severe apnea.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- gamified video-based exercise program (ApneaTheraPlay)
- What this could lead to
- If it works, this could offer a fun, at-home exercise option to help manage sleep apnea symptoms and reduce reliance on CPAP machines.
- What could go wrong
- This is a small, early-stage trial with only 54 participants. The exercises may not improve apnea enough to be clinically meaningful, and long-term adherence is unknown.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Phase
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Not a phased trial
Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.
- Participants
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About 54 people
The number the study aims to enrol. It can still change while the study runs.
- Expected to start
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Jul 2026
An estimate. Start dates often move.
- Expected to finish
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Dec 2027
An estimate. End dates often move.
- Lead sponsor
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Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
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18 to 65 years
- Sex
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Anyone
- Healthy volunteers
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Accepted
You do not need to have the condition being studied to take part.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: * 18-65 years of age * Individuals diagnosed with mild, moderate, or severe OSAS (AHI 5-30 events/hour) based on laboratory diagnostic polysomnography assessments * Individuals diagnosed by a pulmonologist within the last year and who have started CPAP therapy for at most 12 months and who are regular users * Those with habitual snoring * All participants in the exercise group must have or have access to a phone, tablet, or computer compatible with SMART technologies using the exercise system app * Participants must have sufficient physical function to follow the exercise instructions * Familiarity with mobile health applications, as assessed by the VAS, and a willingness to participate in these exercises of \>7 * Not having participated in physiotherapy-based interventions targeting OSAS in the last 3 months * A score of 68 or higher on the System Usability Scale (SUS) Exclusion Criteria: * • BMI \> 40 kg/m2 * Serious drug or alcohol abuse * Regular use of sedatives, muscle relaxants, or opioids that may affect sleep patterns or exercise performance * Pregnancy or postpartum (\<6 months) due to hormonal effects on sleep and respiratory function * Any medical contraindication to physical activity (unstable coronary disease, decompensated heart failure) according to the American College of Sports Medicine (ACSM) exercise guidelines (American College of Sports Medicine, 2021) * History of stroke * Presence of any significant respiratory, neuromuscular, or other disorder causing hypercapnia * Systemic disease associated with an inflammatory entity (e.g., arthritis, sarcoidosis, vasculitis, lupus) * Craniofacial deformity * Presence of secondary respiratory diseases such as severe upper airway obstruction or COPD * Presence of dysphagia * Presence of a frenulum restricting tongue movement
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
How to take part
Only the study team decides who joins. These are the ways to reach them.
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The places running it
1 site. The list below names each one and where it is.
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The official record
ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.
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A doctor treating you
A doctor who knows your case can contact a study site on your behalf, and can tell you whether this study is worth pursuing at all.
Contacts and locations
Locations
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Istanbul Medipol Universty
Istanbul, Göztepe Neighborhood, 34810, Turkey (Türkiye)
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