A Mindfulness-Based Intervention to Improve CPAP

NCT ID: NCT05499286

Last Updated: 2025-05-21

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

ACTIVE_NOT_RECRUITING

Clinical Phase

NA

Total Enrollment

102 participants

Study Classification

INTERVENTIONAL

Study Start Date

2020-06-28

Study Completion Date

2025-09-30

Brief Summary

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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

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Conditions

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Obstructive Sleep Apnea (Moderate to Severe) Obstructive Sleep Apnea

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Primary Study Purpose

OTHER

Blinding Strategy

SINGLE

Investigators

Study Groups

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Mindfulness Program

Participants will attend an online mindfulness program known as the Mindful Awareness and Resilience Skills for Adolescents (MARS-A) program.

Group Type ACTIVE_COMPARATOR

Mindfulness Program

Intervention Type OTHER

Mindful Awareness and Resilience Skills for Adolescents (MARS-A) Curriculum

Online Peer Support Program

Participants will attend an online peer support program where they will engage with each other by sharing experiences while providing advice and emotional support.

Group Type NO_INTERVENTION

No interventions assigned to this group

Interventions

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Mindfulness Program

Mindful Awareness and Resilience Skills for Adolescents (MARS-A) Curriculum

Intervention Type OTHER

Eligibility Criteria

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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
Minimum Eligible Age

13 Years

Maximum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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The Hospital for Sick Children

OTHER

Sponsor Role lead

Responsible Party

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Indra Narang

Principal Investigator

Responsibility Role PRINCIPAL_INVESTIGATOR

Principal Investigators

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Indra Narang, MD

Role: PRINCIPAL_INVESTIGATOR

The Hospital for Sick Children

Locations

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Hospital for Sick Children

Toronto, Ontario, Canada

Site Status

Countries

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Canada

Other Identifiers

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1000068799

Identifier Type: -

Identifier Source: org_study_id

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