Implementation of Home Monitoring in Patients With Pulmonary Fibrosis

NCT06883448 · Status: RECRUITING · Phase: NA · Type: INTERVENTIONAL · Enrollment: 220

Last updated 2025-12-22

No results posted yet for this study

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

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
  • Erasmus Medical Center

    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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Entities

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT06883448 on ClinicalTrials.gov