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Remote Monitoring of Respiratory Health

NCT ID: NCT04739943

Last Updated: 2024-12-11

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

TERMINATED

Clinical Phase

NA

Total Enrollment

20 participants

Study Classification

INTERVENTIONAL

Study Start Date

2021-04-01

Study Completion Date

2021-12-03

Brief Summary

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Recently, interest in ways to monitor and care for patients remotely has significantly increased due to concerns for infection control as well as a way to increase access to regular clinic visits that may be limited for socioeconomic and geographic reasons. However, remote care can be limited by a lack of objective data to help guide clinical care. With respect to respiratory disease, caring for patients remotely may be enhanced by the ability of patients to monitor at home such things as vital signs, lung sounds, and lung function by spirometry. Enhanced methods to follow symptoms and track medication compliance may also be beneficial. These enhancements could improve care and quality of life both for persons with acute respiratory illnesses and those with chronic respiratory disease (such as asthma or COPD).

The purpose of this study is to develop and study methods for patients to monitor their respiratory health at home and make that data available to medical providers to improve their care.

Detailed Description

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Conditions

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Chronic Respiratory Disease Asthma Copd

Keywords

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digital health mobile monitoring

Study Design

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Allocation Method

NA

Intervention Model

SINGLE_GROUP

Participants will be given access to one or more devices or smartphone/tablet applications. They will then be followed with surveys as well as data from chart review to see how use of one or more elements for remote monitoring may affect their quality of life and overall care.
Primary Study Purpose

PREVENTION

Blinding Strategy

NONE

Study Groups

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Mobile Monitoring

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.

Group Type EXPERIMENTAL

Mobile Monitoring

Intervention Type BEHAVIORAL

Participants use a smartphone app for self monitoring of respiratory symptoms

Interventions

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Mobile Monitoring

Participants use a smartphone app for self monitoring of respiratory symptoms

Intervention Type BEHAVIORAL

Eligibility Criteria

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Inclusion Criteria

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

Exclusion Criteria

* people who do not consent
* significant cognitive impairment
* non-English speaking
Minimum Eligible Age

1 Month

Eligible Sex

ALL

Accepts Healthy Volunteers

Yes

Sponsors

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Stanford University

OTHER

Sponsor Role lead

Responsible Party

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R. Sharon Chinthrajah

Associate Professor of Medicine

Responsibility Role PRINCIPAL_INVESTIGATOR

Principal Investigators

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Sharon Chinthrajah, MD

Role: PRINCIPAL_INVESTIGATOR

Stanford University, Sean N. Parker Center for Allergy and Asthma Research

Locations

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Stanford University

Palo Alto, California, United States

Site Status

Countries

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United States

Other Identifiers

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56494

Identifier Type: -

Identifier Source: org_study_id