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Congestive Heart Failure (CHF) clinical trials

View clinical trials related to Congestive Heart Failure (CHF).

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NCT ID: NCT02983812 Completed - Diabetes Clinical Trials

Developing Enhanced Prediction Models

PREDICT
Start date: January 23, 2017
Phase:
Study type: Observational

In this study, patients will be prospectively enrolled for data collection to design prediction models that integrate claims data (inpatient, outpatient, and pharmacy), electronic health record data (on clinical, social, and behavioral indicators), and patient-generated activity data. Patients will be randomized to use either a smartphone or a wearable activity tracking device to capture patient-generated health data.

NCT ID: NCT02369042 Completed - Clinical trials for Congestive Heart Failure(CHF)

KYMA Device: External Measure of Thoracic Fluid and Vital Signs

Ease
Start date: October 2014
Phase: N/A
Study type: Interventional

External measure of thoracic fluid content (TFC) combined with vital signs (HR,respiratory rate(RR), posture and movements) using the technology developed by Kyma Medical Technologies while tracking clinical changes in acute in-hospital and chronic outpatient heart failure patients.

NCT ID: NCT02034045 Completed - Clinical trials for Chronic Obstructive Pulmonary Disease (COPD)

Expanding Paramedicine in the Community

EPIC
Start date: June 2013
Phase: N/A
Study type: Interventional

Initiatives aimed at reducing Emergency Department (ED) wait times and improved community health initiatives are major priorities in Canada. Three of the most common chronic diseases worldwide are Diabetes Mellitus (DM), Congestive Heart Failure (CHF) and Chronic Obstructive Pulmonary Disease (COPD). These diseases are on the rise and currently cost the Canadian health care system billions of dollars every year including the cost of hospitalizations and ED visits. The existing health care system does not have the resources and manpower to effectively care for these patients in the future. Paramedics are currently employed to provide Emergency Medical Services in remote, rural and urban settings in Canada. They are highly trained health care practitioners that are mobile in the community and currently work in a physician medically delegated act model and therefore are positioned to take on new collaborative roles to deliver patient care in the community setting. Increased community paramedic care could decrease the utilization of the health care system resources for patients with chronic disease. Using a randomized control trial design we will attempt to answer the question of whether whether non-emergency community paramedics conducting home visits to undertake assessments and evidence-based treatments of patients in partnership with family doctors will decrease the rate of patient hospitalization.

NCT ID: NCT01960907 Completed - Clinical trials for Chronic Obstructive Pulmonary Disease (COPD)

Clinical Trials for Elderly Patients With Multiple Disease

CHROMED
Start date: October 2013
Phase: N/A
Study type: Interventional

The CHROMED project focuses its investigation on the applicability of an integrated solution for a pathological condition which: a) is very prevalent in ageing patients and b) severely impairs quality of life: COPD with other typical comorbidities such as congestive heart failure and sleep disordered breathing. A specific ICT platform in combination with a set of innovative devices will be used to collect and process useful clinical data at the patient's home and used to optimize their medical treatment. To evaluate the impact of this solution, an international multi-centric randomized control trial will be implemented in five European regions: United Kingdom, Sweden, Estonia, Spain and Slovenia, representing different social and organizational contexts in Europe.

NCT ID: NCT01855022 Completed - Clinical trials for Chronic Obstructive Pulmonary Disease (COPD)

A Trial to Reduce Readmissions Using Motivational Interviewing and Interactive Voice Response

Start date: June 2010
Phase: N/A
Study type: Interventional

The primary purpose of this study is to determine the effectiveness of a hospital-based intervention, using motivational interviewing and interactive voice response (IVR), to reduce hospital readmissions within 90 days of enrollment compared to usual care, for patients with heart failure and chronic obstructive pulmonary disease.

NCT ID: NCT01044290 Completed - Cancer Clinical Trials

Outlook Quality of Life Intervention Study

Start date: January 2011
Phase: N/A
Study type: Interventional

The purpose of this study is to determine whether discussions of life story, forgiveness, and future goals improve quality of life for patients with serious illness.

NCT ID: NCT00734045 Completed - Clinical trials for Congestive Heart Failure (CHF)

Prospective Evaluation of the StatusFirst™ CHF NT-proBNP Device in Human Whole Blood and Plasma Samples

WB-13
Start date: February 2008
Phase: N/A
Study type: Observational

The primary objective of the study is to establish the correlation between NT-proBNP measurements in fresh human whole blood samples and those in plasma samples from the same study subjects, where said samples are collected in EDTA and Li-Hep anticoagulant tubes and measured by the StatusFirst™ CHF NT-proBNP device in conjunction with the DXpressTM Reader in a laboratory setting.

NCT ID: NCT00309764 Completed - Clinical trials for Congestive Heart Failure (CHF)

CHF Management Using Telemedicine

Start date: November 2001
Phase: N/A
Study type: Interventional

The overall objective of this study is to improve clinical outcomes and quality of life for congestive heart failure (CHF) patients by integrating a readily available, low cost technology – the telephone – into coordinated CHF care.

NCT ID: NCT00211874 Completed - Clinical trials for Systolic Dysfunction

Improving Heart Failure Care in Minority Communities

Start date: September 2000
Phase: N/A
Study type: Interventional

For congestive heart failure (CHF) patients with systolic dysfunction, a randomized controlled trial compared nurse-based disease management to address problems in patient and clinician management with usual care for effects on hospitalization and functioning among ethnically-diverse patients in ambulatory practices.