Clinical trial Recruiting at 4 sites Interventional Ages 18 and up

Digital self-management package for people with interstitial lung disease

Official title: A Randomised Clinical Trial of a Digital Self-management Package for People With Interstitial Lung Disease

Run by University of Sydney · NCT06122233 · Data updated 2026-11-12

This study is testing a new smartphone app designed to help people with interstitial lung disease manage their health better and feel improved overall compared to standard care.

Quick facts

Study typeInterventional
Ages18 Years and up
SexAll
Enrollment400 (estimated)
SponsorUniversity of Sydney
Academic / other
Locations4 sites (Sydney, New South Wales and 3 other locations)
StatusRecruiting
StartedJune 3, 2024
Main results expectedJune 2027
Study endsAugust 2027
Registry record updatedApril 4, 2025
Trial IDNCT06122233 on ClinicalTrials.gov

Is this trial a fit for you?

Likely a good fit

Ideal candidates are individuals diagnosed with fibrotic interstitial lung disease who possess a smartphone and have adequate digital literacy.

Probably not a fit

Patients who do not own a smartphone or lack the necessary digital literacy may not benefit from this study.

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

This clinical trial compares a digital self-management package called REBUILD-SM, which includes a smartphone app, to standard care for individuals with interstitial lung disease (ILD). Participants in the intervention group will receive support from healthcare professionals while tracking their health data and completing questionnaires through the app. The study aims to evaluate improvements in health-related quality of life, symptoms, anxiety, self-efficacy, and physical activity over time. The control group will use a limited version of the app without the full self-management support.

Why it matters

Potential benefit: If successful, this approach could significantly enhance the quality of life and self-management capabilities for patients with interstitial lung disease.

How similar studies have gone: Other studies have shown promise in using digital health interventions for chronic disease management, suggesting potential success for this approach.

Who can join: the full rules

Show full inclusion / exclusion criteria
Inclusion Criteria:

* Diagnosis of fibrotic ILD
* In possession of a smartphone/tablet and an email address
* Able to understand written and spoken English
* Adequate digital literacy to complete requirements of trial
* On stable ILD treatment for 30 days prior to enrolment

Exclusion Criteria:

* Not in possession of a smartphone/tablet
* Insufficient digital literacy to complete requirements of trial
* Unable to communicate in written/spoken English
* Not on stable ILD treatment for 30 days prior to enrolment
* Acute exacerbation within 30 days prior to enrolment
* Participating in pulmonary rehab at enrolment or during 12-week intervention period
* Unable to provide informed consent

Where it's running

  • Royal Prince Alfred Hospital
    Sydney, New South Wales, Australia
    Recruiting
  • The Prince Charles Hospital
    Brisbane, Queensland, Australia
    Recruiting
  • Alfred Hospital
    Melbourne, Victoria, Australia
    Recruiting
  • Austin Health
    Melbourne, Victoria, Australia
    Recruiting

Study contacts

Similar studies

Other studies for the same condition or treatment. Recruiting studies are listed first.

  • European database and biobank for childhood interstitial lung diseases

    This study is creating a database and biobank to collect information and samples from children with interstitial lung diseases across Europe to improve their treatment and understanding of these conditions.

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  • AccuPulmo CT Portal for Detecting Pulmonary Fibrosis on Chest CT

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    Recruiting Taichung Veterans General Hospital · Taichung · NCT07761377

  • Advanced imaging to see how immunosuppression affects lung fibrosis activity

    This trial will test whether immunosuppression changes PET and MRI measurements of active collagen deposition and tissue injury in people with non‑IPF interstitial lung disease who are starting treatment.

    Recruiting Phase 2 Massachusetts General Hospital · Boston, Massachusetts · NCT07572383

  • TX000045 for pulmonary hypertension from interstitial lung disease

    This study tests TX000045 to see if it can reduce pulmonary vascular resistance in people with PH caused by interstitial lung disease and to check its safety.

    Recruiting at 12 sites Phase 2 Tectonic Operating Company, Inc. · Phoenix, Arizona and 15 other locations · NCT07473700

  • 68Ga-NI-FAPI-04 PET/CT imaging to detect fibroblast activation in cancer, fibrotic, and heart diseases

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    Recruiting Phase 1/2 Peking Union Medical College Hospital · Beijing, Beijing Municipality · NCT07464132

  • Nebulized human amniotic fluid for interstitial lung disease

    This pilot will try nebulized diluted human amniotic fluid (HAF‑Matrix) in adults 40–90 with interstitial lung disease to check safety and look for early signs of benefit.

    Recruiting Phase 1 Maule Stem Cell Research Institute, Inc. · Venice, Florida · NCT07372989

How to take part

  1. Review the eligibility criteria above with your treating physician.
  2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
  3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.
Last reviewed 2026-11-14 by the Find a Trial editorial team. Information on this page is for educational purposes and is not medical advice. Always consult qualified healthcare professionals about clinical trial participation.