Improving physician adherence in heart failure treatment
Official title: A Prospective Open Randomised Trial to Test the Efficacy of an Assisted Therapy
Run by Medical University Innsbruck · NCT06714344 · Data updated 2026-11-12
This study is testing a new support program to help doctors follow heart failure treatment guidelines better, to see if it can improve patients' health and reduce hospital visits.
Quick facts
| Study type | Interventional |
|---|---|
| Ages | 18 Years and up |
| Sex | All |
| Enrollment | 234 (estimated) |
| Sponsor | Medical University Innsbruck Academic / other |
| Locations | 2 sites (Graz, Styria and 1 other locations) |
| Status | Recruiting |
| Started | December 3, 2024 |
| Main results expected | September 30, 2027 |
| Study ends | September 30, 2027 |
| Registry record updated | February 19, 2025 |
| Trial ID | NCT06714344 on ClinicalTrials.gov |
Is this trial a fit for you?
✓Likely a good fit
Ideal candidates for this study are adults over 18 years old who have been hospitalized for decompensated heart failure and require intravenous diuretics.
✕Probably not a fit
Patients with multimorbidity, dementia, or those unwilling to participate may not benefit from this study.
A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.
What this trial studies
This study evaluates the effectiveness of an Assisted Therapy Optimizing Module designed to enhance physician adherence to guideline-directed medical therapy (GDMT) for heart failure patients. It is a prospective, randomized, multi-sectoral, multi-centre study with a parallel group design. The intervention aims to support network physicians in implementing GDMT, which is often underutilized, particularly in patients enrolled in the telemedicine-supported Herzmobil Tirol program. By improving adherence to GDMT, the study seeks to enhance patient outcomes, including quality of life and reduced hospitalizations.
Why it matters
Potential benefit: If successful, this approach could significantly improve the management of heart failure, leading to better patient outcomes and reduced hospitalizations.
How similar studies have gone: Other studies have shown success in improving adherence to treatment guidelines in chronic conditions, suggesting potential for this approach in heart failure management.
Who can join: the full rules
Show full inclusion / exclusion criteria
Inclusion Criteria: AMPEL, CIP, Version: 1.2 Date: 27.03.2024 1. Written, signed and dated informed consent for inclusion in the HM programme 2. Male and female patients over 18 years of age. 3. Hospitalised for decompensated heart failure requiring intravenous diuretics 4. Need for iv diuresis in nonhospital setting because of impending hospitalization for cardiac decompensation Exclusion Criteria: 1. Multimorbidity (Charlson Comorbidity Index \> 6) 2. Dementia 3. Lack of willingness to participate
Where it's running
-
Medical University of Graz, University Hospital for Internal Medicine (Cardiology)
Graz, Styria, Austria Recruiting -
Medical University of Innsbruck, University Hospital for Internal Medicine III (Cardiology and Angiology)
Innsbruck, Tyrol, Austria Recruiting
Study contacts
- Study coordinator: Gerhard Poelzl, Prof. Dr.
- Email: gerhard.poelzl@tirol-kliniken.at
- Phone: +43 (0)50 504-25621
Similar studies
Other studies for the same condition or treatment. Recruiting studies are listed first.
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This study tests whether using NT-proBNP blood tests to guide heart failure screening in adults 65 and older in rural China can find unrecognized heart problems more effectively than symptom-based screening.
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How to take part
- Review the eligibility criteria above with your treating physician.
- Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
- Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.