Telemedical Interventional Management in patients with Non-Invasive Ventilatio

Not Applicable

• Conditions: J96.1; J96.9; Chronic respiratory failure; Respiratory failure, unspecified

• Registration Number: DRKS00033693
• Lead Sponsor: niversitätsmedizin Essen-Ruhrlandklinik

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Study Start: 2024-02-20
• Last Update Posted: 19 August 2024

Recruitment & Eligibility

• Status: Pending
• Sex: All
• Target Recruitment: 250

Inclusion Criteria

Patients with indication for NIV-initiation due to chronic respiratory insufficiency according to national and international guidelines
Patients who are able and willing to provide their data
Naive to long-term NIV treatment, NIV therapy no longer than 7 days before inclusion into study
Signed informed consent

Exclusion Criteria

Inability to comply with planned study procedures or to comply with study protocol requirements.
Another life-threatening disease (other than chronic respiratory insufficiency and underlying disease) with estimated survival < 12 months

Study & Design

• Study Type: interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
IV-therapy adherence and NIV-associated quality of life by S3-NIV-questionnaire <br><br>Measured at:<br>- initiation of therapy<br>- after 1 month<br>- after 6 months<br>- after 12 months

Secondary Outcome Measures

Name	Time	Method
- Generic and disease-specific quality of life<br>- Number of hospitalisation due to deteriorated health state<br><br>Measured at:<br>- initiation of therapy<br>- after 1 month<br>- after 6 months<br>- after 12 months