Continous Positive Airway Pressure (CPAP) Compliance Study

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

Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.

Recruitment Status

COMPLETED

Clinical Phase

NA

Total Enrollment

50 participants

Study Classification

INTERVENTIONAL

Study Start Date

2012-07-31

Study Completion Date

2012-11-30

Brief Summary

Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.

Does an internet based text or email interaction and education improve CPAP compliance for patients with Obstructive sleep apnea (OSA) and reduce nursing intervention.

Related Clinical Trials

Explore similar clinical trials based on study characteristics and research focus.

Group-based Peer Support Versus Individual Education for Patients Undergoing CPAP Treatment

NCT02538419

Sleep Apnea, Obstructive

COMPLETED NA

Telemonitoring of CPAP Therapy in Sleep Apnea Patients

NCT04868422

Obstructive Sleep Apnea

COMPLETED NA

Intensive Versus Standard Follow up to Improve Continuous Positive Airway Pressure (CPAP) Compliance

NCT02016339

Sleep Apnea

COMPLETED NA

Positive Airway Pressure Program

NCT02331992

Sleep Apnea, Obstructive

COMPLETED NA

Continuous Positive Airway Pressure and Oral Appliances Treatments in Mild Obstructive Sleep Apnea

NCT01461486

Mild Obstructive Sleep Apnea Syndrome

COMPLETED NA

Detailed Description

Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.

Conditions

See the medical conditions and disease areas that this research is targeting or investigating.

Obstructive Sleep Apnea (OSA)

Study Design

Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.

Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Primary Study Purpose

TREATMENT

Blinding Strategy

NONE

Study Groups

Review each arm or cohort in the study, along with the interventions and objectives associated with them.

Standard of care

Participants randomized to this arm will have the usual follow up care without any additional information.

Group Type ACTIVE_COMPARATOR

Standard of care

Intervention Type BEHAVIORAL

participants will receive education from staff nurses as needed.

Additional Education

This arm will receive a weekly text message or e-mail asking participants to sign on to the web page that we will provide. Once they sign on, they will see additional educational materials and questions regarding their CPAP use. Based on their response, they will be directed to suggestion or sites to help improve their compliance with their CPAP.

Group Type ACTIVE_COMPARATOR

additional educational material

Intervention Type BEHAVIORAL

The internet-based intervention group would receive a weekly text or an email (based on the subject's preference). The content of the message asks about their approximate compliance over the past week. Based on their response, they will be directed to one of two internet web pages.

Interventions

Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.

additional educational material

The internet-based intervention group would receive a weekly text or an email (based on the subject's preference). The content of the message asks about their approximate compliance over the past week. Based on their response, they will be directed to one of two internet web pages.

Intervention Type BEHAVIORAL

Standard of care

participants will receive education from staff nurses as needed.

Intervention Type BEHAVIORAL

Eligibility Criteria

Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.

Inclusion Criteria

* Adults (age 18 - 90 years of age) newly diagnosed with OSA who have been recommended CPAP therapy.

Exclusion Criteria

* Previously attempted CPAP, requires the use of bilevel positive airway pressure device, difficulty with English language such that they have difficulty understanding instructions given at high school equivalent, periodic limb movement associated arousals greater than 20/hour, primary complaint of insomnia, diagnosis of restless leg syndrome or periodic limb movement disorder

Minimum Eligible Age

18 Years

Maximum Eligible Age

90 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No