- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06656520
Impact of Telehealth Care
October 22, 2024 updated by: Pei-Hung Liao
Impact of Telehealth Care on Clinical Outcomes in Heart Failure Patients
Heart failure is associated with high incidence and mortality rates, limited physical activity, decreased quality of life, and increased healthcare expenses.
Implementing a Telehealth Care (TC) HF program could address these challenges while improving patient outcomes.
Study Overview
Status
Withdrawn
Conditions
Detailed Description
Telemonitoring for heart failure patients reduces all-cause and cardiovascular mortality by enabling early intervention during clinical deterioration, improving outcomes even for those recently discharged.
Moreover, a reduction in the percentage of days lost due to unplanned cardiovascular hospital admissions is evident.
Furthermore, the rapid expansion of telehealth care and telemedicine services during the COVID-19 pandemic optimized the management and care quality of heart failure patients through telemonitoring .
Study Type
Observational
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
- Child
- Adult
- Older Adult
Accepts Healthy Volunteers
No
Sampling Method
Non-Probability Sample
Study Population
Inpatients diagnosed with heart failure were enrolled, with patients automatically selected daily by the electronic medical record system.
A list of ward visits was obtained based on the first three digits of the International Classification of Diseases 10th edition diagnosis codes; the ICD-10 code I50 was applied for selection.
Description
Inclusion Criteria:
- Inpatients diagnosed with heart failure were enrolled, with patients automatically selected daily by the electronic medical record system. A list of ward visits was obtained based on the first three digits of the International Classification of Diseases 10th edition diagnosis codes; the ICD-10 code I50 was applied for selection.
Exclusion Criteria:
- Other diagnosis
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
mortality and rehospitalization rates
Time Frame: After discharge one year
|
analyze the one-year all-cause mortality and rehospitalization rates in patients with and without telehealth care while examining cardiovascular mortality and rehospitalization rates simultaneously.
|
After discharge one year
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (Actual)
October 2, 2023
Primary Completion (Estimated)
October 2, 2026
Study Completion (Estimated)
October 31, 2026
Study Registration Dates
First Submitted
October 22, 2024
First Submitted That Met QC Criteria
October 22, 2024
First Posted (Actual)
October 24, 2024
Study Record Updates
Last Update Posted (Actual)
October 24, 2024
Last Update Submitted That Met QC Criteria
October 22, 2024
Last Verified
October 1, 2024
More Information
Terms related to this study
Other Study ID Numbers
- 23MMHIS219e
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
NO
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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