- ICH GCP
- Rejestr badań klinicznych w USA
- Badanie kliniczne NCT03902028
Optimized Medico-pharmaceutical Collaboration in the Drug Management of Patients With Heart Failure (COMPIC)
Interest of an Optimized Medico-pharmaceutical Collaboration in the Drug Management of Patients With Heart Failure: Controlled, Randomized, Multicentric Study
Przegląd badań
Status
Warunki
Interwencja / Leczenie
Szczegółowy opis
Heart failure (FH) is a public health problem with an estimated prevalence of about 1.5% in developed countries. In 2013, the number of patients hospitalized in France for heart failure amounted to 165 231 and 20% of them were re-hospitalized at least once for the same reason during this year. Several factors contribute to the occurrence of cardiac decompensation (DC) : some modifiable (age, severity of IC, etiology ...) and others modifiable, such as therapeutics. Various elements could reduce the frequency of re-hospitalizations and the mortality due to this disease :
- a better knowledge of treatments by patients and consequently a better therapeutic compliance
- a better knowledge of the factors and signs of DC (low-sodium diet, weighing...)
- a better implementation of prescribing recommendations : less than 50% of patients have optimal treatment compared to ESC recommendations
- a better communication at the transition points of the patient pathway. The creation of a binomial cardiologist-clinical pharmacist during hospitalization and the maintenance of this optimized multidisciplinary follow-up within 3 months post-hospitalization is a proposal to intervene on these factors. Indeed, the clinical pharmacist (present in the care unit) works in collaboration with the medical and paramedical teams and can improve the care of patients. In the experimental group, a specific multidisciplinary consultation is planned for one month after the end of the hospitalization. A 3-month follow-up visit will be carried out by phone call to meet the criteria for readmission, mortality, quality of life, adherence and persistence of treatments.
Typ studiów
Zapisy (Oczekiwany)
Faza
- Nie dotyczy
Kontakty i lokalizacje
Kontakt w sprawie studiów
- Nazwa: Audrey CASTET-NICOLAS, MCU-PH, Pharm D, PhD
- Numer telefonu: +33 (0)467338564
- E-mail: audrey-castet@chu-montpellier.fr
Kopia zapasowa kontaktu do badania
- Nazwa: Nicolas CHAPET, Pharm D, PhD
- Numer telefonu: (0)467338562
- E-mail: n-chapet@chu-montpellier.fr
Lokalizacje studiów
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Occitanie
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Montpellier, Occitanie, Francja, 34295
- Rekrutacyjny
- University Hospital of Montpellier Cardiology departments oh the Montpellier, Nîmes and Toulouse University Hospitals
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Kontakt:
- Audrey CASTET-NICOLAS, MCU-PH, Pharm D, PhD
- Numer telefonu: (0)467338564
- E-mail: audrey-castet@chu-montpellier.fr
-
Kontakt:
- Nicolas CHAPET, Pharm D
- Numer telefonu: (0)467338562
- E-mail: n-chapet@chu-montpellier.fr
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-
Kryteria uczestnictwa
Kryteria kwalifikacji
Wiek uprawniający do nauki
Akceptuje zdrowych ochotników
Płeć kwalifikująca się do nauki
Opis
Inclusion Criteria:
- Patient aged more than 18 years
- Adult patient admitted in cardiology department (full hospitalisation or intensive care) for heart failure no matter the type and the stage of the disease
- Person affiliated or beneficiary of a social security system
- Collection of a free, informed, express and written consent
Exclusion Criteria:
- Non autonomous drug management patients and not disposing
- a present caregiver during hospitalisation
- Patients living in an institution
- Person participating in another clinical trial with an exclusion period still ongoing
- Person whose physical and/or psychological health is severely altered, and which, in the opinion of the investigator, may affect the participation's to the study
- Person deprived of his rights, person under tutorship or guardianship
- Refusal to sign the consent
Plan studiów
Jak projektuje się badanie?
Szczegóły projektu
- Główny cel: Inny
- Przydział: Randomizowane
- Model interwencyjny: Przydział równoległy
- Maskowanie: Brak (otwarta etykieta)
Broń i interwencje
Grupa uczestników / Arm |
Interwencja / Leczenie |
---|---|
Eksperymentalny: Reinforced multidisciplinary follow-up
Entrance medication reconciliation performed by a pharmacist
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Reinforced multidisciplinary follow-up
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Brak interwencji: Standard care
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Co mierzy badanie?
Podstawowe miary wyniku
Miara wyniku |
Opis środka |
Ramy czasowe |
---|---|---|
Rehospitalisation for heart failure
Ramy czasowe: Call at 3 months after hospitalisation discharge
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At least one rehospitalisation with heart failure related cause
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Call at 3 months after hospitalisation discharge
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Miary wyników drugorzędnych
Miara wyniku |
Opis środka |
Ramy czasowe |
---|---|---|
Prescriptions conformity rates compared to heart failure recommendations edited by the European Society of Cardiology in 2016
Ramy czasowe: At hospitalisation discharge (Day 0)
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Evaluated by a pharmacist
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At hospitalisation discharge (Day 0)
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Prescriptions conformity rates compared to heart failure recommendations edited by the European Society of Cardiology in 2016
Ramy czasowe: Call at 3 months after hospitalisation discharge
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Evaluated by a pharmacist
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Call at 3 months after hospitalisation discharge
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Compliance level
Ramy czasowe: At hospitalisation discharge (Day 0)
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Evaluated by the " Girerd medication adherence questionnaire " The " Girerd medication adherence questionnaire " contains 6 questions which answers are " yes " or " no ". The number of " yes " responses permits to evaluate the level of the patient medication adherence as following : 0 yes : good compliance 1 or 2 yes : minor non compliance 3 or more yes : non compliance |
At hospitalisation discharge (Day 0)
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Compliance level
Ramy czasowe: At 1 month after hospitalisation discharge for the experimental group only
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Evaluated by the "Girerd medication adherence questionnaire" Evaluated by the " Girerd medication adherence questionnaire " The " Girerd medication adherence questionnaire " contains 6 questions which answers are " yes " or " no ". The number of " yes " responses permits to evaluate the level of the patient medication adherence as following : 0 yes : good compliance 1 or 2 yes : minor non compliance 3 or more yes : non compliance |
At 1 month after hospitalisation discharge for the experimental group only
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Compliance level
Ramy czasowe: Call at 3 months after hospitalisation discharge
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Evaluated by the "Girerd medication adherence questionnaire" Evaluated by the " Girerd medication adherence questionnaire " The " Girerd medication adherence questionnaire " contains 6 questions which answers are " yes " or " no ". The number of " yes " responses permits to evaluate the level of the patient medication adherence as following : 0 yes : good compliance 1 or 2 yes : minor non compliance 3 or more yes : non compliance |
Call at 3 months after hospitalisation discharge
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Treatment persistence rates
Ramy czasowe: Call at 3 months after hospitalisation discharge
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Evaluated by a pharmacist
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Call at 3 months after hospitalisation discharge
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Death rate
Ramy czasowe: Call at 3 months after hospitalisation discharge
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Evaluated by a pharmacist
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Call at 3 months after hospitalisation discharge
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Time before death
Ramy czasowe: Call at 3 months after hospitalisation discharge
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Evaluated by a pharmacist
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Call at 3 months after hospitalisation discharge
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Time of occurrence of a potential rehospitalisation related to the disease
Ramy czasowe: Call at 3 months after hospitalisation discharge
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Evaluated by a pharmacist
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Call at 3 months after hospitalisation discharge
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Quality of life score
Ramy czasowe: Call at 3 months after hospitalisation discharge
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Evaluated by the Minnesota Living with Heart Failure Questionnaire the Minnesota Living with Heart Failure Questionnaire contains 21 questions.
Each of the 21 questions ask the patients to indicate how much a possible effect of heart failure have affected their ability to live as wanted during the past month using a scale from 0 (not present or no effect), 1 (very little), 2, 3, 4, or 5 (very much).The measurement of heart failure severity is assessed by summing the responses that ranges from 0 to 105.
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Call at 3 months after hospitalisation discharge
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Satisfaction of the patient
Ramy czasowe: Call at 3 months after hospitalisation discharge
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Evaluated by Likert scale This questionnaire indicates the degree of patient satisfaction using 9 questions which explore the improvement of patient behavior concerning disease and treatment.
The measurement of satisfaction is assessed by summing the responses that range from 9 (unsatisfied) to 36 (very satisfied)
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Call at 3 months after hospitalisation discharge
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Satisfaction of health professionals
Ramy czasowe: online questionnaire at 3 months after hospitalisation discharge
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Evaluated by Likert scale (only for interventional arm) This questionnaire indicates the degree of health professional satisfaction using 6 questions which explore the improvement of transition between hospital to community and comprehension of therapeutic optimization.
The measurement of satisfaction is assessed by summing the responses that range from 6 (unsatisfied) to 24 (very satisfied)
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online questionnaire at 3 months after hospitalisation discharge
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Incremental cost-effectiveness ratio
Ramy czasowe: 3 months after hospitalisation discharge
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3 months after hospitalisation discharge
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Współpracownicy i badacze
Sponsor
Publikacje i pomocne linki
Publikacje ogólne
- Ponikowski P, Voors AA, Anker SD, Bueno H, Cleland JGF, Coats AJS, Falk V, Gonzalez-Juanatey JR, Harjola VP, Jankowska EA, Jessup M, Linde C, Nihoyannopoulos P, Parissis JT, Pieske B, Riley JP, Rosano GMC, Ruilope LM, Ruschitzka F, Rutten FH, van der Meer P; ESC Scientific Document Group. 2016 ESC Guidelines for the diagnosis and treatment of acute and chronic heart failure: The Task Force for the diagnosis and treatment of acute and chronic heart failure of the European Society of Cardiology (ESC)Developed with the special contribution of the Heart Failure Association (HFA) of the ESC. Eur Heart J. 2016 Jul 14;37(27):2129-2200. doi: 10.1093/eurheartj/ehw128. Epub 2016 May 20. No abstract available. Erratum In: Eur Heart J. 2016 Dec 30;:
- Jackevicius CA, de Leon NK, Lu L, Chang DS, Warner AL, Mody FV. Impact of a Multidisciplinary Heart Failure Post-hospitalization Program on Heart Failure Readmission Rates. Ann Pharmacother. 2015 Nov;49(11):1189-96. doi: 10.1177/1060028015599637. Epub 2015 Aug 10.
- Available at: https://academic.oup.com/eurheartj/article/37/27/2129/1748921/2016-ESC-Guidelines-for-the-diagnosis-and. (Accessed: 12th September 2017).
- Masters J, Morton G, Anton I, Szymanski J, Greenwood E, Grogono J, Flett AS, Cleland JG, Cowburn PJ. Specialist intervention is associated with improved patient outcomes in patients with decompensated heart failure: evaluation of the impact of a multidisciplinary inpatient heart failure team. Open Heart. 2017 Mar 8;4(1):e000547. doi: 10.1136/openhrt-2016-000547. eCollection 2017.
- Van Spall HGC, Rahman T, Mytton O, Ramasundarahettige C, Ibrahim Q, Kabali C, Coppens M, Brian Haynes R, Connolly S. Comparative effectiveness of transitional care services in patients discharged from the hospital with heart failure: a systematic review and network meta-analysis. Eur J Heart Fail. 2017 Nov;19(11):1427-1443. doi: 10.1002/ejhf.765. Epub 2017 Feb 24.
- Lopez Cabezas C, Falces Salvador C, Cubi Quadrada D, Arnau Bartes A, Ylla Bore M, Muro Perea N, Homs Peipoch E. Randomized clinical trial of a postdischarge pharmaceutical care program vs regular follow-up in patients with heart failure. Farm Hosp. 2006 Nov-Dec;30(6):328-42. doi: 10.1016/s1130-6343(06)74004-1. English, Spanish.
- Parajuli DR, Franzon J, McKinnon RA, Shakib S, Clark RA. Role of the Pharmacist for Improving Self-care and Outcomes in Heart Failure. Curr Heart Fail Rep. 2017 Apr;14(2):78-86. doi: 10.1007/s11897-017-0323-2.
- Wan TTH, Terry A, Cobb E, McKee B, Tregerman R, Barbaro SDS. Strategies to Modify the Risk of Heart Failure Readmission: A Systematic Review and Meta-Analysis. Health Serv Res Manag Epidemiol. 2017 Apr 18;4:2333392817701050. doi: 10.1177/2333392817701050. eCollection 2017 Jan-Dec.
- Buckley MS, Harinstein LM, Clark KB, Smithburger PL, Eckhardt DJ, Alexander E, Devabhakthuni S, Westley CA, David B, Kane-Gill SL. Impact of a clinical pharmacy admission medication reconciliation program on medication errors in "high-risk" patients. Ann Pharmacother. 2013 Dec;47(12):1599-610. doi: 10.1177/1060028013507428. Epub 2013 Oct 15.
- Warden BA, Freels JP, Furuno JP, Mackay J. Pharmacy-managed program for providing education and discharge instructions for patients with heart failure. Am J Health Syst Pharm. 2014 Jan 15;71(2):134-9. doi: 10.2146/ajhp130103.
Daty zapisu na studia
Główne daty studiów
Rozpoczęcie studiów (Rzeczywisty)
Zakończenie podstawowe (Oczekiwany)
Ukończenie studiów (Oczekiwany)
Daty rejestracji na studia
Pierwszy przesłany
Pierwszy przesłany, który spełnia kryteria kontroli jakości
Pierwszy wysłany (Rzeczywisty)
Aktualizacje rekordów badań
Ostatnia wysłana aktualizacja (Rzeczywisty)
Ostatnia przesłana aktualizacja, która spełniała kryteria kontroli jakości
Ostatnia weryfikacja
Więcej informacji
Terminy związane z tym badaniem
Słowa kluczowe
Dodatkowe istotne warunki MeSH
Inne numery identyfikacyjne badania
- RECHMPL18_0040
Informacje o lekach i urządzeniach, dokumenty badawcze
Bada produkt leczniczy regulowany przez amerykańską FDA
Bada produkt urządzenia regulowany przez amerykańską FDA
Te informacje zostały pobrane bezpośrednio ze strony internetowej clinicaltrials.gov bez żadnych zmian. Jeśli chcesz zmienić, usunąć lub zaktualizować dane swojego badania, skontaktuj się z register@clinicaltrials.gov. Gdy tylko zmiana zostanie wprowadzona na stronie clinicaltrials.gov, zostanie ona automatycznie zaktualizowana również na naszej stronie internetowej .
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