Team-Based care may cut hospital readmissions for a common heart failure
NCT ID NCT07798856
First seen Sep 01, 2026 · Last updated Sep 02, 2026 · Updated 1 time
Summary
This trial tests whether a coordinated care team, including cardiologists, pharmacists, dietitians, and rehabilitation specialists, can improve outcomes for people hospitalized with heart failure with preserved ejection fraction (HFpEF). Participants receive structured follow-up, medication review, dietary and lifestyle counseling, and exercise guidance. Researchers compare their hospital stay length, readmission rates, and quality of life against a historical group that received standard care. The goal is to see if this integrated approach reduces hospitalizations and improves daily living for a condition with limited treatment options.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- Multidisciplinary Integrated Care Model (MICM), a structured team-based care program including cardiology management, case management, pharmacist-led medication review, nutritional counseling, and exercise guidance
- What this could lead to
- If it works, this integrated care approach could reduce hospital readmissions and improve quality of life for people with HFpEF, a condition with few effective treatments.
- What could go wrong
- This is a quasi-experimental study with a historical control group, which is less reliable than a randomized trial. The results may be influenced by differences between the groups, and the intervention may not be widely applicable.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Phase
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Not a phased trial
Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.
- Participants
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About 200 people
The number the study aims to enrol. It can still change while the study runs.
- Expected to start
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Aug 2026
An estimate. Start dates often move.
- Expected to finish
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Oct 2027
An estimate. End dates often move.
- Lead sponsor
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Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
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18 years and older
- Sex
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Anyone
- Healthy volunteers
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Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: * Age 18 years or older * Hospitalized with a physician diagnosis of heart failure with preserved ejection fraction (HFpEF) * Left ventricular ejection fraction (LVEF) ≥50% on echocardiography performed during the index hospitalization * New York Heart Association (NYHA) functional class III to IV * Able to communicate in Mandarin or Taiwanese and understand the study intervention * For the prospective intervention group: willing to participate and provide written informed consent. For the historical control group: existing medical record data will be collected under a waiver of informed consent. Exclusion Criteria: * Patients who elected hospice or palliative care as part of an advance care plan during the index hospitalization * Severe cognitive impairment without a family member or caregiver available to assist with the digital platform * Anticipated inability to complete post-discharge follow-up or lack of regular follow-up at the study institution's outpatient clinic * Length of index hospital stay less than 24 hours
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
How to take part
Only the study team decides who joins. These are the ways to reach them.
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The places running it
1 site. The list below names each one and where it is.
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The official record
ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.
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A doctor treating you
A doctor who knows your case can contact a study site on your behalf, and can tell you whether this study is worth pursuing at all.
Contacts and locations
Locations
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Chi Mei Medical Center
Tainan, Yongkang Dist, 71004, Taiwan
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