NCT03035123Completed
Therapeutic Education Strategy for Patients With Acute Heart Failure
Impact of an Intensive Therapeutic Education on Occurrence of Clinical Events in Patients With Acute Heart Failure: EduStra-HF Study
Source: ClinicalTrials.gov · Last updated 3 Apr 2025
Brief summary (registry, in English)
The EduStra-HF study will examine the impact of an intensive therapeutic education on patients discharged from hospital after an episode of acute heart failure (HF). Patients will be randomized into two groups: one will receive "usual care" monitoring and one will receive a specific educational monitoring programme for 1 year. All patients will meet with a specialized therapeutic education nurse before discharge. The effect of the intensive education on HF rehospitalization and quality of life will be examined.
- Status (registry)
- Completed
- Study type
- Interventional
- Enrollment
- 318 (actual)
- First submitted
- 5 Dec 2016
- Start date
- 1 Apr 2017
- Primary completion date
- 30 Dec 2023
- Lead sponsor
- Resicard
- Diseases
- Heart failure
- NCT number
- NCT03035123
What you commit to
- Study type: Interventional
- Participants enrolled: 318
- From 1 Apr 2017 to the primary completion date, 30 Dec 2023
- 6 sites in 1 country
- Visits and tests: ask the trial team, the registry does not list them
Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.
Who cannot take part
Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.
Prior treatment
- Cardiac surgery in the previous 3 months
- Medical or surgical procedure which might interfere with monitoring
Other illness
- Active cancer
- Severe psychiatric or neurological disorder
- Complicated acute myocardial infarction
- Significant valvular diseases requiring surgery
- Planned heart transplant
Other
- Psychosocial:
- Refusal to accept the study design
- Patient under guardianship
- Monitoring obstacle: language, cognitive deficiency, itinerant lifestyle, regular travel, institutionalization
- Inability to sign the consent form or to complete questionnaires
- Medical:
- Hypertrophic obstructive cardiomyopathy
- Enrollment in another clinical trial
Who the study is looking for
- Adult patient with acute HF
- Affiliated to the French Social Security system
- Accepting the principle of telephone monitoring
- Accepting home visits from a study nurse
- Possession of a mobile phone
Age in the registry: 18 years to - · Sex: All · Does not accept healthy volunteers
Sites (6)
Sites in registry order. Pick your city on the disease page to sort them by distance.
| Site | City | Country | Site status |
|---|---|---|---|
| Clinique Ambroise Pare Coordinator of this site? Confirm its status | Neuilly-sur-Seine | France | Unknown status |
| Institut Mutualiste Montsouris Coordinator of this site? Confirm its status | Paris | France | Unknown status |
| Clinique du Mont Louis Coordinator of this site? Confirm its status | Paris | France | Unknown status |
| Hopital AP-HP Saint-Antoine Coordinator of this site? Confirm its status | Paris | France | Unknown status |
| Centre Cardiologique du Nord Coordinator of this site? Confirm its status | Saint-Denis | France | Unknown status |
| Centre Hospitalier André Mignot Coordinator of this site? Confirm its status | Versailles | France | Unknown status |
This page is information, not medical advice. Discuss any trial with your doctor.