Telemedicine for Heart Failure: Evaluation of Treatment, Prognosis and Patient Experience
This study aims to observe the impact of telemedicine on heart failure patients, focusing on general health, hospitalizations, mortality rates, and the number of out-patient clinical care contacts.
Data Collection
Collected from today forward - ProspectiveCardiovascular Diseases
+ Heart Diseases
+ Heart Failure
Case-Control
Comparing exposures between individuals with and without disease in order to identify potential risk factors.Summary
Study start date: April 15, 2020
Actual date on which the first participant was enrolled.Heart failure (HF) is a condition that affects many people, especially those over 80 years old. It can cause significant healthcare costs and suffering. Traditional treatment involves frequent physical visits to specialized clinics to adjust medications. However, recent advances in technology have made telemonitoring possible, where health data is wirelessly transmitted from sensors. This study aims to evaluate if telemonitoring can provide effective, safe, and cost-efficient care with high patient satisfaction for HF patients. It's important because it could improve care, reduce hospitalizations, and enhance quality of life for HF patients. The study uses real-world data from the Swedish national HF register, SwedeHF, and electronic health records to optimize patient selection, equipment, and protocols, as recommended by the European Society of Cardiology's (ESC) guidelines for HF, 2021. Adult HF patients from specialized clinics are being recruited. They receive equipment to report vital signs and patient experience measures, automatically transmitted via smartphone for six months. A digital application is used for data registration and communication with healthcare providers. Medication adjustments may be done remotely. Abnormal values trigger notifications to healthcare providers, who offer services during office hours. Physical visits are planned as needed. A matched control population is obtained from the SwedeHF registry. Data is collected from medical records, questionnaires, and national registers. Outcomes include mortality, healthcare needs, patient experience, time to and dosages at optimal medical therapy. Health economic outcomes and management systems are also evaluated. Data analysis uses traditional regression models and machine learning techniques to identify predictive factors for death and rehospitalization.
Protocol
This section provides details of the study plan, including how the study is designed and what the study is measuring.300 patients to be enrolled
Total number of participants that the clinical trial aims to recruit.Case-Control
Eligibility
Researchers look for people who fit a certain description, called eligibility criteria: person's general health condition or prior treatments.Any sex
Biological sex of participants that are eligible to enroll.Over 18 Years
Range of ages for which participants are eligible to join.Healthy volunteers not allowed
If individuals who are healthy and do not have the condition being studied can participate.Conditions
Pathology
Criteria
Study Plan
Find out more about all the medication administered in this study, their detailed description and what they involve.Study Objectives
Primary Objectives
Secondary Objectives
Study Centers
These are the hospitals, clinics, or research facilities where the trial is being conducted. You can find the location closest to you and its status.This study has 1 location
Sahlgrenska University Hospital
Gothenburg, SwedenOpen Sahlgrenska University Hospital in Google Maps