A Mindfulness-Based Intervention to Improve CPAP
- Conditions
- Obstructive Sleep Apnea (Moderate to Severe)Obstructive Sleep Apnea
- Interventions
- Other: Mindfulness Program
- Registration Number
- NCT05499286
- Lead Sponsor
- The Hospital for Sick Children
- Brief Summary
The main purpose of this study is to assess the effectiveness of a mindfulness-based intervention in improving CPAP use compared to online peer support
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ACTIVE_NOT_RECRUITING
- Sex
- All
- Target Recruitment
- 102
- Adolescent age (13-18 years)
- Confirmed diagnosis of moderate or severe OSA
- Adolescent should have the capacity to consent themselves
- Known developmental delay such that they are not able to participate in the study;
- Neuromuscular disorders
- Central sleep apnea
- Known diagnosis of severe psychiatric illnesses (e.g. suicidal ideation)
- Limited knowledge and proficiency in English to complete the study as judged by the clinical team
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- PARALLEL
- Arm && Interventions
Group Intervention Description Mindfulness Program Mindfulness Program Participants will attend an online mindfulness program known as the Mindful Awareness and Resilience Skills for Adolescents (MARS-A) program.
- Primary Outcome Measures
Name Time Method The effectiveness of MBI for CPAP adherence. Week 4-12 The primary objective is to evaluate the effectiveness of a mindfulness-based intervention (MBI) in improving CPAP adherence in adolescents with OSA when compared to online peer support. Adherence to CPAP will be measured objectively as hours of usage of CPAP per night.
- Secondary Outcome Measures
Name Time Method The effects of increased adherence on mental, physical, and psychosocial statuses. Week 4-12 Evaluate the effects of increased CPAP adherence on daytime sleepiness, HRQOL, psychosocial functioning and mental health status (e.g. anxiety and depression). This will be measured by administering questionnaires at baseline, before intervention, after intervention and again at follow-up.
Trial Locations
- Locations (1)
Hospital for Sick Children
🇨🇦Toronto, Ontario, Canada