Telemedicine and Ventilator Titration in Chronic Respiratory Patients Initiating Non-invasive Ventilation

NCT ID: NCT01560741

Last Updated: 2012-10-04

Basic Information

• Recruitment Status: UNKNOWN
• Clinical Phase: PHASE1
• Total Enrollment: 128 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2012-07-31
• Study Completion Date: 2013-05-31

Brief Summary

The critical nature of respiratory diseases, the continuously increasing prevalence of these conditions, and the subjective perception of patients vis-à-vis their pulmonary function and health status underscore the importance of home telemonitoring. These conditions are critical and necessitate close and regular monitoring that may be achieved at distance using telemonitoring. This study will assess a number of measures both at baseline and post-intervention from a number of domains, including Arterial Blood Gases (ABG), BiPAP-related data, chronic respiratory failure symptoms, health-related quality of life, patients satisfaction and utilization of healthcare resources.

Detailed Description

In recent years home care is becoming increasingly used and considered by some the future of healthcare. Home mechanical ventilation has been shown to improve morbidity and mortality in patients with chronic respiratory failure of different aetiologies. A French survey suggests an increase of 12% of cases per year. With the prospect of a substantial increase of ventilated patients at home, facilities and resources have not been proportionally growing, so new approaches should be investigated and addressed to absorb this constant flux of patients.

Telemedicine is defined as the broad use of electronic and communications technologies to provide and support remote monitoring of health status. It has been shown to be an effective alternative model of care for managing chronic diseases. It as also been shown to reduce healthcare costs and is a major topic on the agendas of health and social care policies in Europe.

Home telemonitoring of respiratory conditions results in early identification of deteriorations in patient condition and symptom control.

However, evidence on the magnitude of clinical and structural effects remains preliminary, with variations in study approaches and an absence of robust study designs and formal evaluations.

The objective is gathering data that can be help to establish guidelines for non invasive home mechanical ventilation initiation and quality control.

Conditions

Chronic Obstructive Pulmonary Disease; Neuromuscular Disease; Chest Wall Disorders; Obesity Hypoventilation Syndrome

Keywords

Chronic respiratory failure; Noninvasive Mechanical Ventilation; Home-care; Telemedicine; COPD

Study Design

• Allocation Method: RANDOMIZED
• Intervention Model: PARALLEL
• Primary Study Purpose: TREATMENT
• Blinding Strategy: DOUBLE

Study Groups

Telemedicine Group

Patients will be initiated and adapted on non-invasive home mechanical ventilation in Pulmonology Department of S. João Hospital, in an outpatient setting, according to the prevailing standard of care for Chronic Respiratory Diseases patients in this unit. Patients will be provided with a ventilator outfitted with a wireless transmitter to allow the remote data collection of compliance and efficacy information. While patient sleeps, data is collected. If abnormalities criteria will be detected, remote titration of ventilator settings will be done to optimise therapy. Patient will be monitored again and data analyzed. This procedure will be repeated until we obtained the optimal ventilator parameters for each patient in this group. Nocturnal oximetry under home mechanical non-invasive ventilation will be carried out after one week and one month of treatment. Subjects also receive pre-arranged telephone calls to assist with progress.

Group Type: ACTIVE_COMPARATOR

Telemonitoring tools

Intervention Type: DEVICE

Patients will go home with telemedicine tools to monitor efficacy and compliance of non-invasive home mechanical ventilation

Usual care

Patients will be initiated and adapted on non-invasive home mechanical ventilation in Pulmonology Department of S. João Hospital, in an outpatient setting, according to the prevailing standard of care for Chronic Respiratory Diseases patients in this unit. Patients will be assessed by a hospital visit scheduled at the end of third month after their initial adaptation. In this hospital visit data provided by the ventilator will be transferred to research team computer so they could evaluate patient compliance and efficacy of ventilation criteria under the parameters used at home present at the time of assessment. If abnormality criteria will be detected, re-titration of ventilator settings will be made. Patients will be encouraged to call their respiratory consultant any time they had a problem or concern.

Group Type: OTHER

Usual Care

Intervention Type: DEVICE

The assessment of efficacy and compliance will be monitor at the end of third month. This is the date of the scheduled hospital visit.

Interventions

Telemonitoring tools

Patients will go home with telemedicine tools to monitor efficacy and compliance of non-invasive home mechanical ventilation

Intervention Type: DEVICE

Usual Care

The assessment of efficacy and compliance will be monitor at the end of third month. This is the date of the scheduled hospital visit.

Intervention Type: DEVICE

Other Intervention Names

wireless transmiter; Hospital visit

Eligibility Criteria

Inclusion Criteria

OHS:

• PaCO2 > 45 mmHg;
• IMC > 40 Kg/m2

COPD:

• Age < 80 years;
• Receiving appropriate medical therapy according to gold guidelines
• Long-term oxygen therapy (LTOT) for at least 3 months;
• PaCO2 > 50 mmHg during room air
• ph > 7,35 and free from exacerbations in the 4 weeks preceding recruitment;
• One exacerbation in the last year before preceding recruitment with necessity of NIV in the acute care setting;
• FEV1 < 1,5l or < 50% predicted;
• FEV1/FVC < 60%
• Total Lung Capacity (TLC)≥ 90% predicted;
• PaO2 < 60 mmHg breathing room air at rest.

NMD and CWD:

• PaCO2 > 45 mmHg;
• Significant nocturnal desaturation
• FVC < 50% predicted;
• SNIP < 40 cmH20
• MIP < 60% predicted
• Ortopnea;
• 20% drop of VC in supine position.

Exclusion Criteria

OHS:

• COPD
• NMD

COPD:

• 15% increase in FEV1 after inhaled Salbutamol (200 µg);
• Active smoking;
• History of OSA (with AHI > 15 episodes.h-1)

NMD and CWD:

• COPD;
• OHS;
• PCF < 270;
• Severe bulbar weakness (ALSFRS bulbar subscore 0-3)
• MIC/VC=1

• Minimum Eligible Age: 15 Years
• Maximum Eligible Age: 80 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: No

Sponsors

Hospital Sao Joao

OTHER

Sponsor Role: lead

Responsible Party

Miguel R. Goncalves

Clinical Professor

Responsibility Role: PRINCIPAL_INVESTIGATOR

Principal Investigators

J C Winck, Phd

Role: PRINCIPAL_INVESTIGATOR

Hospital de S. João

Locations

Hospital de S.João

Porto, Porto District, Portugal

Site Status: RECRUITING

Countries

Portugal

Central Contacts

João Carlos Winck, PhD

Role: CONTACT

Phone: +351 225 512 100

Email: jcwfc@hsjoao.min-saude.pt

Miguel Gonçalves, PhD

Role: CONTACT

Phone: +351 225 512 100

Email: goncalvesmr@gmail.com

Other Identifiers

TeleMotiNIV2012

Identifier Type: -

Identifier Source: org_study_id