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A Mindfulness-Based Intervention to Improve CPAP

Not Applicable
Active, not recruiting
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
Inclusion Criteria
  • Adolescent age (13-18 years)
  • Confirmed diagnosis of moderate or severe OSA
  • Adolescent should have the capacity to consent themselves
Exclusion Criteria
  • 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
GroupInterventionDescription
Mindfulness ProgramMindfulness ProgramParticipants will attend an online mindfulness program known as the Mindful Awareness and Resilience Skills for Adolescents (MARS-A) program.
Primary Outcome Measures
NameTimeMethod
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
NameTimeMethod
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

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