A randomized controlled trial for investigating a novel integrated care concept (NICC) for patients suffering from chronic cardiovascular disease: CardioCare MV

Organizational Data

DRKS-ID:
DRKS00013124
Recruitment Status:
Recruiting complete, study continuing
Date of registration in DRKS:
2017-10-05
Last update in DRKS:
2019-11-26
Registration type:
Prospective

Acronym/abbreviation of the study

CardioCare MV

URL of the study

http://www.cardiocare-mv.de

Brief summary in lay language

Cardiovascular diseases are the number 1 cause of death globally and represent a major economic burden on health care systems. We have developed a novel integrated care concept (NICC) which combines telemedicine with intensive support by a call center, an integrated care network including in- and outpatient care providers and guideline therapy for patients with heart failure (HF), atrial fibrillation (AF) or therapy resistant hypertension (TRH). The aim of the study is to show that NICC is preferable over guideline therapy alone. We aim at including approximately 890 patients. Patients could be enrolled either directly at the Care-Center (location: University Hospital of Rostock) or at one of the advanced treatments rooms of the Care-Center (outpatient cardiological specialist practices). The ethics commission's statement of the University of Rostock is available for amendment 2 since 20.08.2019 at the number A2017-0117.

Brief summary in scientific language

Background: Cardiovascular diseases are the number 1 cause of death globally and represent a major economic burden on health care systems. Positive effects of disease management programs have been shown for patients with heart failure (HF). Remote monitoring and telemonitoring with active intervention are beneficial in atrial fibrillation (AF) and therapy resistant hypertension (TRH), respectively. For these patients, we have developed a novel integrated care concept (NICC) which combines telemedicine with intensive support by a call center, an integrated care network including in- and outpatient care providers and guideline therapy for patients. Methods: The aim of the study is to demonstrate the superiority of NICC over guideline therapy alone. The trial is designed as open-label bi-center parallel-group design with two groups. Patients will only be included who will be accompanied by their general practitioner and/or specialist during the clinical trial (cooperating care provider in the sense of a IV-contract according to §140 SGB V). Randomization will be done individually with stratification by cardiovascular disease (AF, HF, TRH), center and admission type. Primary endpoints are based on the 1-year observation period after randomization. The first primary endpoint is the composite endpoint consisting of mortality, stroke and myocardial infarction. The number of hospitalizations form the second primary endpoint. The third primary endpoint is identical to the first primary endpoint plus cardiac decompensation. Adjustments for multiple testing are done using a fall back strategy. Secondary endpoints include patient adherence, health care costs, quality of life and safety. The power for the second primary endpoint is 80% at the two-sided 2.5% test-level with a sample size of 890 patients. Discussion: This study will inform care providers whether quality of care can be improved by an integrated care concept providing telemedicine through a 24/7 care center approach. We expect that cost of the NICC will be lower than standard care because of reduced hospitalizations. If the study has a positive result, NICC is planned to be immediately rolled out in the state of Mecklenburg-West Pomerania. The trial will also guide additional research to disentangle the effects of this complex intervention.

Health condition or problem studied

ICD10:
I50 - Heart failure
ICD10:
I10 - Essential (primary) hypertension
ICD10:
I48 - Atrial fibrillation and flutter
Healthy volunteers:
No Entry

Interventions, Observational Groups

Arm 1:
Novel integrated care concept (NICC): The care center is at the heart of the NICC structure. It will be available 24/7. It is the core platform to share information for all NICC patients in the care process and serves as integration point between the professional groups. The care center is utilizing the NICC platform for care coordination and patient monitoring. The NICC platform enables patient management from the distance and allows treating physicians to observe and follow the health status of patients daily. Using the NICC tablet, patients provide information from home about their health status. They will receive feedback about their therapy, measurements and reminders and motivation to follow care plans. The communication allows for a regular evaluation of the patient's situation, a review of the therapy and coordination of necessary adjustments with care providers. The general intervention rules are based on the current European Society of Cardiology (ESC) guidelines for treating AF, HF and TRH patients. Every patient is treated for 1 year with NICC.
Arm 2:
Standard care: guideline therapy according to the European Society of Cardiology Guideline AF: Kirchhof et al. (2016 Eur Heart J). Guideline HF: Ponikowski et al. (2016 Eur Heart J) Guideline for TRH follows guideline for arterial hypertension Mancia et al. (2013 Eur Heart J). Follow-up per patient: 1 year.

Endpoints

Primary outcome:
First primary endpoint: composite endpoint consisting of mortality, stroke and myocardial infarction within the 1-year observation period. Second primary endpoint: number of hospitalizations within the 1-year observation period. Third primary endpoint: composite endpoint consisting of mortality, stroke, myocardial infarction and cardiovascular decompensation within the 1-year observation period.
Secondary outcome:
Quality of life: measured at baseline, after 6 months and 1 year; measured with EQ-5D-5L. NYHA stadium, EHRA stadium, number of antihypertensives, blood pressure at the end of the 1-year observation period. Treatment cost within the 1-year observation period, measured with data provided by health insurance company. Safety: measure after 1 year; measured as mortality, stroke, TIA, myocardial infarction, hospitalization, cardiovascular decompensation. Standard inventories: measured at baseline, after 6 months and 1 year, such as well-being (WHO-5). Adherence to NICC; measured continuously (daily), e.g., frequency of transfer of measurements. Association between adherence to NICC and outcome.

Study Design

Purpose:
Treatment
Allocation:
Randomized controlled study
Control:
  • Active control (effective treatment of control group)
Phase:
N/A
Study type:
Interventional
Mechanism of allocation concealment:
No Entry
Blinding:
No
Assignment:
Parallel
Sequence generation:
No Entry
Who is blinded:
No Entry

Recruitment

Recruitment Status:
Recruiting complete, study continuing
Reason if recruiting stopped or withdrawn:
No Entry

Recruitment Locations

Recruitment countries:
  • Germany
Number of study centers:
Multicenter study
Recruitment location(s):
  • Medical center HELIOS Kliniken Schwerin Schwerin
  • University medical center Rostock

Recruitment period and number of participants

Planned study start date:
2017-12-01
Actual study start date:
2017-12-04
Planned study completion date:
No Entry
Actual Study Completion Date:
No Entry
Target Sample Size:
964
Final Sample Size:
964

Inclusion Criteria

Sex:
All
Minimum Age:
18 Years
Maximum Age:
no maximum age
Additional Inclusion Criteria:
1. Heart failure (I50, NYHA II-IV) or atrial fibrillation (I48, EHRA II-IV) or resistant hypertension (I10-15, ≥ 3 antihypertensive medicines from different drug classes, SBP > 140 /90mmHg or ≥ 4 antihypertensives irrespective of the blood pressure, with at least one drug being a diuretic). 2. Member of health insurance company AOK Nordost or Techniker Krankenkasse (TK). 3. Inscription to integrated care contract with the health insurance company. 4. Residence in Mecklenburg-Vorpommern. 5. Age ≥ 18 years. 6. Written informed consent.

Exclusion Criteria

1. Pregnancy, suspected pregnancy or breast-feeding period. 2. Participation in another clinical trial up to 30 days before inclusion in this trial. 3. Cognitive deficits: patients need to be able to read and understand German language as presented on a tablet. 4. Chronic kidney disease requiring dialysis or creatinine clearance < 15 ml/min.

Addresses

Primary Sponsor

Address:
Universitätsmedizin Rostock
Prof. Dr. Christian Schmidt
Ernst-Heydemann-Str. 8
18055 Rostock
Germany
Telephone:
+49 381 494 5011
Fax:
+49 381 494 5012
Contact per E-Mail:
Contact per E-Mail
URL:
http://med.uni-rostock.de
Investigator Sponsored/Initiated Trial (IST/IIT):
Yes

Contact for Scientific Queries

Address:
AMEDON GmbH
Dr. Katja Krockenberger
Willy-Brandt-Allee 31C
23554 Lübeck
Germany
Telephone:
+49 451 38450262
Fax:
No Entry
Contact per E-Mail:
Contact per E-Mail
URL:
http://amedon.de

Contact for Public Queries

Address:
Universitätsmedizin Rostock Versorgungsstrukturen GmbH
Dr Miriam Mann
Ernst-Heydemann-Str. 8
18057 Rostock
Germany
Telephone:
+49 381 494 5073
Fax:
No Entry
Contact per E-Mail:
Contact per E-Mail
URL:
No Entry

Principal Investigator

Address:
AMEDON GmbH
Dr. Katja Krockenberger
Willy-Brandt-Allee 31C
23554 Lübeck
Germany
Telephone:
+49 451 38450262
Fax:
No Entry
Contact per E-Mail:
Contact per E-Mail
URL:
http://amedon.de

Sources of Monetary or Material Support

Public funding institutions financed by tax money/Government funding body (German Research Foundation (DFG), Federal Ministry of Education and Research (BMBF), etc.)

Address:
Gemeinsamer Bundesausschuss
Postfach 120606
10596 Berlin
Germany
Telephone:
No Entry
Fax:
No Entry
Contact per E-Mail:
Contact per E-Mail
URL:
No Entry

Private sponsorship (foundations, study societies, etc.)

Address:
Techniker Krankenkasse
Postfach 110 565
19005 Schwerin
Germany
Telephone:
No Entry
Fax:
No Entry
Contact per E-Mail:
Contact per E-Mail
URL:
No Entry

Private sponsorship (foundations, study societies, etc.)

Address:
AOK Nordost - Die Gesundheitskasse
Behlertstraße 33 A
14467 Potsdam
Germany
Telephone:
No Entry
Fax:
No Entry
Contact per E-Mail:
Contact per E-Mail
URL:
No Entry

Ethics Committee

Address Ethics Committee

Address:
Ethikkommission an der Medizinischen Fakultät der Universität Rostock im Institut für Rechtsmedizin
St.-Georg-Str. 108
18055 Rostock
Germany
Telephone:
+49-381-4949904
Fax:
+49-381-4949902
Contact per E-Mail:
Contact per E-Mail
URL:
No Entry

Vote of leading Ethics Committee

Vote of leading Ethics Committee
Date of ethics committee application:
2017-07-17
Ethics committee number:
A 2017-0117
Vote of the Ethics Committee:
Approved
Date of the vote:
2017-07-18

Further identification numbers

Other primary registry ID:
NCT03317951 - ClinicalTrials.gov
EudraCT Number:
No Entry
UTN (Universal Trial Number):
No Entry
EUDAMED Number:
No Entry

IPD - Individual Participant Data

Do you plan to make participant-related data (IPD) available to other researchers in an anonymized form?:
No Entry
IPD Sharing Plan:
No Entry

Study protocol and other study documents

Study protocols:
No Entry
Study abstract:
No Entry
Other study documents:
No Entry
Background literature:
No Entry
Related DRKS studies:
No Entry

Publication of study results

Planned publication:
No Entry
Publikationen/Studienergebnisse:
No Entry
Date of first publication of study results:
No Entry
DRKS entry published for the first time with results:
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Basic reporting

Basic Reporting / Results tables:
No Entry
Brief summary of results:
No Entry