Remote Monitoring for Interstitial Lung Disease

This study is testing different ways to monitor people with fibrotic interstitial lung disease (f-ILD) from home. This includes conditions like Idiopathic Pulmonary Fibrosis (IPF) and other types of lung fibrosis. You would use devices like a spirometer (to measure breathing), a pulse oximeter (to check oxygen levels), and/or a wireless scale, all connected to your phone. Researchers want to see which combination of these tools works best to detect important changes in your health. To join, you need to be 18 or older, speak English or Spanish, and have a UCSF diagnosis of a major ILD type. The study aims to find out how well these tools can spot new health events and how consistently people use them over 12 months. The current recruitment status is unclear.

Study design
This is an interventional study with a planned enrollment of 200 participants. It is not specified if it is randomized or blinded.
What's involved
You would have an initial in-person visit and a final in-person visit at the UCSF clinic. Other follow-up visits at 3, 6, and 9 months will be done remotely via Zoom. You will use study-provided home monitoring devices weekly (spirometry for all, some also daily pulse oximetry and/or weekly weight measurements) and complete electronic questionnaires for 12 months.
Compensation
Not stated in the trial record.
Follow-up
Participants will be monitored for 12 months, with primary endpoints measured at Baseline and Month 12.

AI-generated from the public study record. Only the study team can confirm whether you're eligible — confirm details with them before making decisions.

NCT07673237

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

Not Yet Recruiting
NAAges 18+InterventionalHealth services
University of California, San Francisco
~200 participants
Updated 2026-06-29 on ClinicalTrials.gov
What's tested:Home Monitoring in Patients with f-ILD

At a glance

Recruiting sites
0 of 1 listed site is recruiting right now
RecruitingSuspended, closed, or not yet open
What they're measuring
Detection rate of clinically significant ILD events
Measured over Baseline, Month 12
+4 more outcomes measured
Fibrotic Interstitial Lung Disease
IPF and PPF
Lung Fibrosis Interstitial

NCT07673237

Where you'd take part

This study runs at 1 site. They're the same protocol — you choose where, and that choice sets who your contact draft is addressed to.

  • University of California, San Francisco

    San Francisco, Californiano site contact published

Sites open and close at different times, so the status above is per site — it can differ from the study's overall status.

  • Erica Farrand, MD · PRINCIPAL_INVESTIGATOR · University of California, San Francisco

Opens a ready-to-send draft in your own email app — review before sending.

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Eligibility criteria

Inclusion

age 18 or older
English or Spanish speaking
have a UCSF diagnosis of one of the major ILD subtypes seen in the ILD Clinic (Idiopathic Pulmonary Fibrosis, Chronic Hypersensitivity Pneumonitis, Connective-tissue disease related ILD, Sarcoidosis, Familial Fibrosis). Languages are limited to those for which both device instructional materials and user support are available (written and video). The ILD diagnosis will be based on multidisciplinary conference review, which is the diagnostic gold standard. We have restricted the ILD subtypes to those for which there is efficacy data for RPM or comparable clinical trajectories, and subtypes that account for \>10% of the ILD diagnoses seen at UCSF.

Exclusion

Patients who are unable provide informed consent for any reason or are acutely ill.
  • Detection rate of clinically significant ILD eventsBaseline, Month 12

    Measured using a composite endpoint of acute exacerbation, hospitalization, or rapid disease progression, defined as a ≥10% relative decline in FVC over 3 months

  • Time to detection of first ILD eventBaseline, Month 12

    Measured using a composite endpoint of acute exacerbation, hospitalization, or rapid disease progression, defined as a ≥10% relative decline in FVC over 3 months.

  • Adherence12 months

    Adherence to remote monitoring protocol, defined as the proportion of measurements completed \>=67% of weeks with full data entry)

  • Retention12 months

    Primary: Participant retention at 12 months (target \>=80%)

  • Data Completeness12 months

    Data completeness, defined as \>85% of expected remote monitoring data points successfully transmitted