Daily home monitoring in Idiopathic Pulmonary Fibrosis * a pilot study to assess feasibility of a home spirometry and eHealth self-management application

Daily home monitoring in Idiopathic Pulmonary Fibrosis * a pilot study to assess feasibility of a home spirometry and eHealth self-management application - Home monitoring in IPF

Status

Active, not recruiting

Phases

Unknown

Study type

Observational

Source

NL-OMON

Registry ID

NL-OMON45619

Enrollment

Registered

2017-08-07

Start date

2017-11-03

Completion date

Unknown

Last updated

2024-02-28

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

idiopathic pulmonary fibrosis lung fibrosis

Interventions

e-health

home monitoring

home spirometry

idiopathic pulmonary fibrosis

Eligibility

Age

18 Years to 64 Years

Inclusion criteria

Inclusion criteria: All patients with a diagnosis of IPF according to the ATS 2011 criteria

Exclusion criteria

Exclusion criteria: not able to speak, read or write in Dutch no access to the internet

Design outcomes

Primary

Measure	Time frame
Adherence to home monitoring and reproducibility of home spirometry will be measured to assess feasibility.	—

Secondary

Measure	Time frame
- Correlation between home spirometry and hospital based measurements of lung function - Exploratory endpoints are patient satisfaction with the care process and the effect of home monitoring on different parameters of HRQOL.	—

Countries

The Netherlands

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)