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Mobile Monitoring Device for Respiratory Disorders

N/A

Waitlist Available

Led By Sharon Chinthrajah, MD

Research Sponsored by Stanford University

Eligibility Criteria Checklist

Specific guidelines that determine who can or cannot participate in a clinical trial

Must have

age 1 month or older with a diagnosis of chronic respiratory disease (ex. asthma, COPD), an acute respiratory illness or a healthy volunteer

Age 1 month or older with a diagnosis of chronic respiratory disease (ex. asthma, COPD), an acute respiratory illness or a healthy volunteer

Must not have

Significant cognitive impairment

Non-English speaking

Timeline

Screening 3 weeks

Treatment Varies

Follow Up up to 2 years

Awards & highlights

No Placebo-Only Group

Summary

This trial is looking at ways to help patients with respiratory disease monitor their symptoms and compliance with medication at home, as well as their vital signs, lung sounds, and lung function.

Who is the study for?

This trial is for individuals aged 1 month or older with chronic respiratory diseases like asthma or COPD, acute respiratory illnesses, or even healthy volunteers. Participants must be able to give consent themselves or through a parent if underage and speak English. Those with significant cognitive impairment cannot join.

What is being tested?

The study is testing the use of mobile monitoring devices that allow patients to track their respiratory health at home. This data will then be used by medical providers to potentially improve patient care and overall quality of life.

What are the potential side effects?

Since this trial involves non-invasive remote monitoring devices, there are no direct side effects from medications as in drug trials. However, participants may experience inconvenience or discomfort associated with using these devices regularly.

Eligibility Criteria

Inclusion Criteria

You may be eligible if you check “Yes” for the criteria below

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I am over 1 month old and have a chronic respiratory condition, an acute respiratory illness, or am healthy.

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I am over 1 month old and have a chronic respiratory condition, an acute respiratory illness, or am healthy.

Exclusion Criteria

You may be eligible for the trial if you check “No” for criteria below:

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I have significant memory or thinking problems.

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I do not speak English.

Timeline

Screening ~ 3 weeks3 visits

Treatment ~ Varies

Follow Up ~ up to 2 years

Screening ~ 3 weeks

Treatment ~ Varies

Follow Up ~up to 2 years

This trial's timeline: 3 weeks for screening, Varies for treatment, and up to 2 years for reporting.

Treatment Details

Study Objectives

Study objectives can provide a clearer picture of what you can expect from a treatment.

Primary study objectives

Asthma Control Test (ACT)

PROMIS-10 survey

Awards & Highlights

No Placebo-Only Group

All patients enrolled in this study will receive some form of active treatment.

Trial Design

1Treatment groups

Experimental Treatment

Group I: Mobile MonitoringExperimental Treatment1 Intervention

Participants will be asked to use a smartphone or tablet application for remote monitoring or respiratory health. They will be followed over time with surveys as well as chart review to assess effects of adding these mobile monitoring elements to their standard care.

0 / 4Eligibility criteria met