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Therapeutic Education Strategy for Patients With Acute Heart Failure (EduStra-HF)

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ClinicalTrials.gov Identifier: NCT03035123
Recruitment Status : Recruiting
First Posted : January 27, 2017
Last Update Posted : January 31, 2019
Sponsor:
Collaborators:
Agence Regionale de Sante d'Ile de France
Assistance Publique - Hôpitaux de Paris
French Cardiology Society
Novartis
Information provided by (Responsible Party):
Pr Ariel Cohen, Saint Antoine University Hospital

Brief Summary:

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.


Condition or disease Intervention/treatment Phase
Heart Failure Behavioral: Therapeutic education Not Applicable

Detailed Description:

The prevalence of HF in France is increasing. According to a report from the Haute Autorité de Santé (HAS) - the French Health Authority - published in June 2015 concerning discharge of patients hospitalized for HF, 2.3% of the French adult population is affected. Despite improvements in treatment and HF-specific care, the rehospitalization rate for HF remains substantial, and HF management is a major public health issue.

Chronic HF leads to psychological and physiological issues in patients. Furthermore, this disease affects patient quality of life and activities of daily living.

The HAS also reported that even if iterative hospitalizations are the consequence of complicated and multifactorial situations, some could be prevented by improved patient care.

The aim of the EduStra-HF study is to examine the effect of an intensive therapeutic education on patients discharged from hospital after an episode of acute HF. It will study whether this intervention reduces the rate of rehospitalization and increases quality of life in this population.

To achieve this goal, a multicentre, randomized, two parallel arm study will be conducted. Patients will be included in several cardiology centres in Paris (Ile-de-France) over 2 years and 3 months.

Included patients, chosen from patients admitted for acute HF in the participating hospitals, will be randomized into two groups, which will determine the monitoring they receive after discharge. For each patient, monitoring will last for 1 year from the day they return home.

The first group of patients will be randomized to receive "usual care" monitoring and will not be given specific therapeutic education after discharge.

The second group (intervention arm) will receive a specific educational monitoring programme from nurses via telephone calls and home visits, for 1 year. Monitoring will began early after discharge. Annual medical monitoring and visits to the cardiologist will also be planned.

All patients, regardless of attribution arm, will meet a nurse trained in therapeutic education during their stay in hospital. Moreover, validated and HF-related self-assessed questionnaires will be analyzed to assess quality of life and impact of HF on patient activities of daily living.

In the interventional arm, patients will receive monitoring documents, such as a HF information booklet and a personal monitoring agenda.

The EduStra-HF study will provide a specific analysis of a multisupport therapeutic education (including medical monitoring). Data on all HF drug treatments, including the more recent ones (e.g. Entresto), blood tests results, and cardiologic data will be recorded.


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Study Type : Interventional  (Clinical Trial)
Estimated Enrollment : 1086 participants
Allocation: Randomized
Intervention Model: Parallel Assignment
Masking: None (Open Label)
Primary Purpose: Supportive Care
Official Title: Impact of an Intensive Therapeutic Education on Occurrence of Clinical Events in Patients With Acute Heart Failure: EduStra-HF Study
Actual Study Start Date : April 1, 2017
Estimated Primary Completion Date : December 30, 2020
Estimated Study Completion Date : December 30, 2020

Resource links provided by the National Library of Medicine

MedlinePlus related topics: Heart Failure

Arm Intervention/treatment
No Intervention: "Usual care"
Patients will attend an appointment with the therapeutic education nurse before discharge, after which they will have no further contact with the education team. The Research team members will telephone the patient three times during the year (after 2, 6 and 12 months) to collect data on HF treatments, blood tests results, health-related events and hospitalizations.
Experimental: Interventional

Before discharge, patients will attend an appointment with a nurse trained in therapeutic education, in which the nurse will evaluate the overall knowledge and the skills of the patient about HF. The nurse will then define specific educational objectives with the patient, based on the patient's medical history, state of disease, comorbidities, alarm signs, fears and knowledge.

Each patient will receive six telephone calls and two home-visits during the 1 year of follow-up. Each contact between the nurse and the patient will be dedicated to HF education. The patient will also receive regular short text messages containing health advice and appointment reminders.

To help the patient regain his/her autonomy, intervals between education sessions will be progressively longer.

Behavioral: Therapeutic education
Interventional arm




Primary Outcome Measures :
  1. Number of rehospitalizations for acute heart failure (HF) in both groups of patients [ Time Frame: 1 year ]

Secondary Outcome Measures :
  1. Patients knowledge about the illness [ Time Frame: 1 year ]
    Nurses will evaluate during each telephone call and home visit patients knowledge and skills about the following items : illness, treatments, diet, physical activity, medical follow-up. This data will be recorded in a specific table and classified into "acquired / partially acquired / not acquired" items.

  2. Global quality of life [ Time Frame: 1 year ]
    Assessed by validated questionnaire SF-12

  3. Quality of life linked to Heart Failure [ Time Frame: 1 year ]
    Assessed by validated questionnaire KCCQ-15

  4. Length of stay for HF and all-cause hospitalizations [ Time Frame: 1 year of follow-up ]
  5. Hospitalization rate for cardiovascular diseases except HF [ Time Frame: 1 year of follow-up ]
  6. Cardiovascular and all-cause mortality rate [ Time Frame: 1 year of follow-up ]
  7. B-type natriuretic peptide (BNP) or NT pro-BNP levels [ Time Frame: During 1 year of follow-up ]

Other Outcome Measures:
  1. Cost effectiveness of the intervention [ Time Frame: During 1 year of follow-up ]
    Comparison between both groups of patients of the HF-hospitalizations average cost, related to the operating cost of the EduStra-HF method.



Information from the National Library of Medicine

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Ages Eligible for Study:   18 Years and older   (Adult, Older Adult)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   No
Criteria

Inclusion Criteria:

  • 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

Exclusion Criteria:

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:

  • Active cancer
  • Severe psychiatric or neurological disorder
  • Complicated acute myocardial infarction
  • Significant valvular diseases requiring surgery
  • Hypertrophic obstructive cardiomyopathy
  • Planned heart transplant
  • Cardiac surgery in the previous 3 months
  • Enrollment in another clinical trial
  • Medical or surgical procedure which might interfere with monitoring

Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT03035123


Contacts
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Contact: Ariel Cohen, MD PhD +33149282886 ariel.cohen@aphp.fr
Contact: Patrick Assyag, MD +33143798361 patrick.assyag@wanadoo.fr

Locations
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France
Clinique Ambroise Paré Recruiting
Neuilly-sur-Seine, France, 92200
Principal Investigator: Olivier Belliard, MD         
Clinique du Mont Louis Terminated
Paris, France, 75011
Hopital AP-HP Saint-Antoine Recruiting
Paris, France, 75012
Principal Investigator: Ariel Cohen, MD PhD         
Hôpital AP-HP Pitié-Salpêtrière Withdrawn
Paris, France, 75013
Institut Mutualiste Montsouris Recruiting
Paris, France, 75014
Principal Investigator: Christelle Diakov, MD         
Centre Cardiologique du Nord Recruiting
Saint Denis, France, 93200
Principal Investigator: Thierry Laperche, MD         
Centre Hospitalier André Mignot Recruiting
Versailles, France, 78000
Principal Investigator: Jean-Louis George, MD         
Sponsors and Collaborators
Resicard
Agence Regionale de Sante d'Ile de France
Assistance Publique - Hôpitaux de Paris
French Cardiology Society
Novartis
Investigators
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Principal Investigator: Ariel Cohen, MD PhD Hôpital Saint-Antoine

Additional Information:
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Responsible Party: Pr Ariel Cohen, Head of the cardiology department, Saint Antoine University Hospital
ClinicalTrials.gov Identifier: NCT03035123     History of Changes
Other Study ID Numbers: EduStra-HF
RCB ID: 2016-A00899-42 ( Other Grant/Funding Number: National Drug and Health Products Safety Agency (ANSM) )
First Posted: January 27, 2017    Key Record Dates
Last Update Posted: January 31, 2019
Last Verified: January 2019
Individual Participant Data (IPD) Sharing Statement:
Plan to Share IPD: Undecided
Plan Description: Sharing Individual Participant Data requires a specific authorization from the French Board CNIL (Commission Nationale de l'Informatique et des Libertés) which chooses whether to allow the research team to share patient data. A specific request is needed and will be sent to that authority.

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Studies a U.S. FDA-regulated Drug Product: No
Studies a U.S. FDA-regulated Device Product: No

Keywords provided by Pr Ariel Cohen, Saint Antoine University Hospital:
Heart Failure
Therapeutic education
Quality of life

Additional relevant MeSH terms:
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Heart Failure
Heart Diseases
Cardiovascular Diseases