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RECRUITING
NCT07673237
NA

Remote Evaluation and Surveillance of Patients With Interstitial Lung Disease: Transforming ILD Care Delivery With Remote Monitoring

Sponsor: University of California, San Francisco

View on ClinicalTrials.gov

Summary

The purpose of this interventional study is to identify which combination of remote monitoring devices (e.g. home spirometry, pulse oximetry, scale, ePROs) is the most feasible (as defined by adherence, retention, and data completeness) and acceptable when used for the detection of clinically significant Interstitial Lung Disease events.

Key Details

Gender

All

Age Range

18 Years - Any

Study Type

INTERVENTIONAL

Enrollment

200

Start Date

2026-10-01

Completion Date

2028-08-01

Last Updated

2026-10-08

Healthy Volunteers

No

Interventions

DEVICE

Spirometer

Home spirometry will be conducted weekly by completing a spirometry maneuver (inhaling and exhaling through the device mouthpiece).

DEVICE

Oximeter

Oxygen saturation levels will be measured daily using a pulse oximeter.

DEVICE

Scale

Weight will be measured weekly using a wireless scale provided by the study.

OTHER

ePROs (electronic patient reported outcomes)

Brief electronic symptom questionnaires will be completed through a secure app which will be downloaded on participant's phone.

Locations (1)

University of California, San Francisco

San Francisco, California, United States