Implementation of Home Monitoring in Patients With Pulmonary Fibrosis
NCT06883448 · Status: RECRUITING · Phase: NA · Type: INTERVENTIONAL · Enrollment: 220
Last updated 2025-12-22
Summary
The objective of this study is to evaluate the impact of structurally replacing half of the outpatient clinic visits for patients with pulmonary fibrosis by home monitoring and video consultations on patient self-management and health(care) outcomes.
Conditions
- Pulmonary Fibrosis
- Interstitial Lung Disease (ILD)
Interventions
- COMBINATION_PRODUCT
-
Home monitoring care
Patients in the home monitoring group will receive a home spirometer, pulse oximetry meter, and access to a smartphone or tablet app, where they can perform home based measurements weekly and complete PROMs. Furthermore, this app includes disease specific information and allows for direct communication with the hospital via eConsultation. In the home monitoring group, half of the outpatient clinic visits will alternately be replaced by remote visits via video consultation.
Sponsors & Collaborators
-
Zuyderland Medisch Centrum, Sittard-Geleen, the Netherlands
collaborator UNKNOWN -
Leiden University Medical Center, LUMC, Leiden, The Netherlands
collaborator UNKNOWN -
UMC Utrecht, Utrecht, the Netherlands
collaborator UNKNOWN -
Rijnstate, Arnhem, the Netherlands
collaborator UNKNOWN -
Catharina, Eindhoven, the Netherlands
collaborator UNKNOWN -
MC Leeuwarden, Leeuwarden, the Netherlands
collaborator UNKNOWN -
OLVG, Amsterdam, the Netherlands
collaborator UNKNOWN -
Medical Center Haaglanden, The Hague, The Netherlands
collaborator UNKNOWN -
Amphia, Breda, the Netherlands
collaborator UNKNOWN -
St. Antonius Hospital
collaborator OTHER - lead OTHER
Principal Investigators
-
Marlies S. Wijsenbeek-Lourens, Prof Dr · Department of Respiratory Medicine, Center of Excellence for Interstitial Lung Disease, Erasmus University Medical Center, Rotterdam, The Netherlands
Study Design
- Allocation
- RANDOMIZED
- Purpose
- HEALTH_SERVICES_RESEARCH
- Masking
- NONE
- Model
- PARALLEL
Eligibility
- Min Age
- 18 Years
- Sex
- ALL
- Healthy Volunteers
- No
Timeline & Regulatory
- Start
- 2024-10-02
- Primary Completion
- 2026-09-01
- Completion
- 2026-09-01
Countries
- Netherlands
Study Locations
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