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The purpose of this pilot study is to evaluate a remote patient monitoring (RPM) system using a daily PRO tool (EXACT = Exacerbations of Chronic Pulmonary Disease Tool), in preventing hospitalization from Chronic Obstructive Pulmonary Disease (COPD) exacerbations in a COPD population at high risk of exacerbation, compared to those managed by usual care.
This study uses two parallel groups of approximately 100 patients in each arm. After a screening period to confirm eligibility, patients will be randomized to either the RPM system group, or the usual care group. Both groups will be followed for 52 weeks until the end of study. There are only 4 planned study visits and patients will continue on their usual treatment.
The remote patient monitoring system will issue an alert to the clinical site once the established threshold change has been reached. The alert notification will require the clinical site to contact the patient and treat the patient based on clinical judgment and clinical practice. Patients in the usual care arm will be managed through their normally nurse/physician contact.
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| Remote patient monitoring | Experimental | Remote patient monitoring system including the Exacerbations of Chronic Pulmonary Disease Tool (EXACT) tool can use changes in daily scores over a certain threshold level to alert notification to the clinical site. The site will contact the patient in order to determine the clinical significance associated with the change in score, and to treat the patient based on clinical judgment and clinical practice. |
|
| Usual care | Experimental | This group of patient will continue on their usual standard care as close to real life situation as possible. |
|
| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| Remote Patient Monitoring | Device | Remote patient monitoring system including exacerbations of chronic pulmonary disease Tool - Patient Reported Outcome (EXACT PRO), Lung Monitor, and Pulse Oximeter |
| Measure | Description | Time Frame |
|---|---|---|
| The number of hospitalizations and emergency room visits for management of COPD exacerbation(s) | Comparison of the total number of hospitalizations and emergency room visits (combined) for management of Chronic Obstructive Pulmonary Disease (COPD) exacerbation(s) between the two arms | 52 weeks |
| Measure | Description | Time Frame |
|---|---|---|
| Lenght of hospitalization | Comparison of the average length of hospital stay for management of COPD exacerbation(s) between the two arms. | 52 weeks |
| Time to first hospitalization | Comparison of the time to first occurrence of hospitalization for management of COPD exacerbation(s) between the two arms. |
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Inclusion Criteria:
Exclusion criteria:
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| Name | Affiliation | Role |
|---|---|---|
| Novartis Pharmaceuticals | Novartis Pharmaceuticals | Study Director |
| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| Novartis Investigative Site | Barcelona | Catalonia | 08025 | Spain | ||
| Novartis Investigative Site |
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| Label | URL |
|---|---|
| Results for CIDD001D2401 can be found on the Novartis Clinical Trial Results Website | View source |
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| Usual care | Other | Patients in the usual care arm will continue their normally established procedures of nurse/physician contact and evaluation, as is considered standard for each individual practitioner in the study. |
|
| 52 weeks |
| Use of health care resources | Comparison of the combined health care resource utilization (hospitalizations, unscheduled, scheduled office visits, telephone call contacts) for management of COPD between the two arms. | 52 weeks |
| Number of medical visits | Comparison of the number of medical visits combined (hospitalizations, emergency room visits, unscheduled and scheduled office visits) for management of COPD between the two arms. | 52 weeks |
| Barcelona |
| Catalonia |
| 08035 |
| Spain |
| Novartis Investigative Site | Barcelona | Catalonia | 08036 | Spain |
| Novartis Investigative Site | Girona | Catalonia | 17007 | Spain |
| Novartis Investigative Site | L'Hospitalet de Llobregat | Catalonia | 08907 | Spain |
| Novartis Investigative Site | Lleida | Catalonia | 25198 | Spain |
| Novartis Investigative Site | Sant Boi de Llobregat | Catalonia | 08830 | Spain |
| Novartis Investigative Site | Sant Cugat del Vallès | Catalonia | 08190 | Spain |
| Novartis Investigative Site | Sant Joan Despí | Catalonia | 08970 | Spain |
| Novartis Investigative Site | Majadanonda | Madrid | 28220 | Spain |
| Novartis Investigative Site | Madrid | 28034 | Spain |
| Novartis Investigative Site | Madrid | 28040 | Spain |
| Novartis Investigative Site | Torremolinos | 29620 | Spain |
| Novartis Investigative Site | Gagnef | 785 21 | Sweden |
| Novartis Investigative Site | Gothenburg | Sweden |
| Novartis Investigative Site | Kungshamn | 456 31 | Sweden |
| Novartis Investigative Site | Lund | 222 22 | Sweden |
| Novartis Investigative Site | Lund | SE-221 85 | Sweden |
| Novartis Investigative Site | Östersund | 831 83 | Sweden |
| Novartis Investigative Site | Stockholm | 113 61 | Sweden |
| ID | Term |
|---|---|
| D029424 | Pulmonary Disease, Chronic Obstructive |
| ID | Term |
|---|---|
| D008173 | Lung Diseases, Obstructive |
| D008171 | Lung Diseases |
| D012140 | Respiratory Tract Diseases |
| D002908 | Chronic Disease |
| D020969 | Disease Attributes |
| D010335 | Pathologic Processes |
| D013568 | Pathological Conditions, Signs and Symptoms |
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