Completed

Telemedicine for Heart Failure: Evaluation of Treatment, Prognosis and Patient Experience

0 criteria met from your profileSee at a glance how your profile meets each eligibility criteria.
Study Aim

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.

What is being collected

Data Collection

Collected from today forward - Prospective
Who is being recruted

Cardiovascular Diseases

+ Heart Diseases

+ Heart Failure

Over 18 Years
+8 Eligibility Criteria
See all eligibility criteria
How is the trial designed

Case-Control

Comparing exposures between individuals with and without disease in order to identify potential risk factors.
Observational
Study Start: April 2020
See protocol details

Summary

Principal SponsorSahlgrenska University Hospital
Last updated: January 28, 2026
Sourced from a government-validated database.Claim as a partner

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.

Official TitleTelemedicine in Heart Failure: Studies of Treatment, Prognosis and Patient Experience
NCT06237998
Principal SponsorSahlgrenska University Hospital
Last updated: January 28, 2026
Sourced from a government-validated database.Claim as a partner

Protocol

This section provides details of the study plan, including how the study is designed and what the study is measuring.
Design Details

300 patients to be enrolled

Total number of participants that the clinical trial aims to recruit.

Case-Control

These studies compare people who have a disease (cases) with those who don't (controls). The goal is to look back at previous exposures or risk factors to identify what might have contributed to the disease.

Eligibility

Researchers look for people who fit a certain description, called eligibility criteria: person's general health condition or prior treatments.
Conditions
Criteria

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

Cardiovascular DiseasesHeart DiseasesHeart Failure

Criteria

8 exclusion criteria prevent from participating
Insufficient understanding of spoken or written Swedish, and no access to assistance

Lacking cognitive and physical ability to handle equipment and make measurements

Not motivated to participate

Does not hold a national digital identification: Mobilt BankID

Show More Criteria

Study Plan

Find out more about all the medication administered in this study, their detailed description and what they involve.
Study Objectives

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

Suspended

Sahlgrenska University Hospital

Gothenburg, SwedenOpen Sahlgrenska University Hospital in Google Maps
CompletedOne Study Center