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Intensive Education on Lipid Management

Primary Purpose

Acute Coronary Syndrome

Status
Unknown status
Phase
Not Applicable
Locations
China
Study Type
Interventional
Intervention
Intensive Education
Control
Sponsored by
Junbo Ge
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Acute Coronary Syndrome focused on measuring acute coronary syndrome, statins, LDL-C, intensive education

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  1. The patients admitted to the hospital with a diagnosis of ACS including those for first consulting or with recurrence. The patient was prescribed atorvastatin (Lipitor®) by physicians in hospital;
  2. The age of patient enrolled will be ≥18 years old;
  3. The patient is able to understand and complete questionnaire.
  4. The patients agree to accept follow-up visits, and willing to participate in patient education courses and sign informed consent form.

Exclusion Criteria:

  1. The patient has contraindications to statins, such as active hepatic disease, patient has a history of intolerance or hypersensitivity to statins or has a history of prior rhabdomyolysis on a statin.
  2. The patient who uses other statins except Lipitor® when discharged from the hospital;
  3. Cardiac function class of the patient is class IV(NYHA);
  4. The patient has a malignant tumor;
  5. The patient has a severe arrhythmia.

Sites / Locations

  • Fujian Medical University Union Hospital
  • The 2nd affiliated hospital of harbin medical university
  • Xi'an Jiaotong University College of Medicine
  • The Luhe Teaching Hospital of the Capital Medical University
  • Shanghai Zhongshan Hospital

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Sham Comparator

Arm Label

Intensive Educational Group

Control Group

Arm Description

The Intensive Educational Group will receive 5 visits, including 2 visits via phone contacts. The expected dates for each visit will be stamped on the follow-up brochure for convenience. Patient education in this group includes routine education at discharge; 4 educational brochures, a calendar with health tips, and follow-up brochure with medical expert letter sent to patients at the day for discharge (baseline); and educational short messages through message platform once a week. Dosage and adjustment of statins, and concomitant medications in all the treated patients will be recorded.

The Control Group will receive 3 visits and receive care as per usual practice by the treating doctor and a follow-up brochure without medical expert letter. Dosage and adjustment of statins, and concomitant medications in all the treated patients will be recorded. Blood lipid panel (4 items), hepato-renal functions, and creatine kinase will be examined; while, Morisky 8-item questionnaire will be used to evaluate medication compliance at outpatient visits. In addition, the occurrence of major cardiovascular events and AE/SAE will be collected during the study.

Outcomes

Primary Outcome Measures

LDL-C target achieving rate

Secondary Outcome Measures

LDL-C target achieving rate
the proportions of patients with statin persistence
the proportions of patients with statin persistence
statin compliance
statin compliance
the relationship of LDL-C target achieving rate and statin compliance
the discontinuation reason of statin therapy
the difference of LDL-C control rate and statin compliance
To find the difference of LDL-C control rate and statin compliance between pre-specified sub-groups: PCI or non-PCI/male or female/age (≥65) or not/ having medical insurance or not/dyslipidemia history or not /MI (myocardial infarction) or UA (unstable angina)/different risk level according to TIMI/ patients for first consulting or patients with recurrence/ have received statin in the last 3 months or not.

Full Information

First Posted
August 15, 2013
Last Updated
August 18, 2013
Sponsor
Junbo Ge
Collaborators
Fujian Medical University, The Second Affiliated Hospital of Harbin Medical University, Health Science Center of Xi'an Jiaotong University, The Luhe Teaching Hospital of the Capital Medical University
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1. Study Identification

Unique Protocol Identification Number
NCT01925079
Brief Title
Intensive Education on Lipid Management
Official Title
A Randomized and Controlled Study About the Impact of Intensive Education on Lipid Management in Patients With Acute Coronary Syndrome in China
Study Type
Interventional

2. Study Status

Record Verification Date
August 2013
Overall Recruitment Status
Unknown status
Study Start Date
August 2013 (undefined)
Primary Completion Date
February 2015 (Anticipated)
Study Completion Date
June 2015 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor-Investigator
Name of the Sponsor
Junbo Ge
Collaborators
Fujian Medical University, The Second Affiliated Hospital of Harbin Medical University, Health Science Center of Xi'an Jiaotong University, The Luhe Teaching Hospital of the Capital Medical University

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
Among the patients with coronary heart disease, those with ACS (acute coronary syndrome) are extremely high-risk patients. Therefore, management outside hospital, especially the regular administration of drugs, is vital to prevent the recurrence of cardiovascular events. However, most patients often fail to stay on a long-term administration regimen, especially the administration of statins. According to the statistics, the average duration adhered with statin in patients with ACS is less than 3 months, use of statin at hospital discharge was only 80% and 65% in 6 month, with a very low LDL-C control rate (about 11% at 6 months), which poses a threat to the recurrence rate of cardiovascular events in patients with ACS. It was found in previous studies that there were many factors influencing patients' compliance, in which patients' refusing to take medicine accounted for a higher proportion. It suggests that patient had not recognized the importance of long-term administration. Therefore, it is extremely important for physicians to strengthen patient education and regular follow-up visits during disease management. Moreover, the effectiveness of patient education during chronic disease management has already been proved in some studies abroad, and the interventional effect of multiple patient education process outweighs that of single approach education. Thus, we intend to conduct a randomized and controlled study to explore the effect of multi-channel intensive patient education on LDL-C target achieving rate and statin adherence in patients with ACS in China.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Acute Coronary Syndrome
Keywords
acute coronary syndrome, statins, LDL-C, intensive education

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
2568 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Intensive Educational Group
Arm Type
Experimental
Arm Description
The Intensive Educational Group will receive 5 visits, including 2 visits via phone contacts. The expected dates for each visit will be stamped on the follow-up brochure for convenience. Patient education in this group includes routine education at discharge; 4 educational brochures, a calendar with health tips, and follow-up brochure with medical expert letter sent to patients at the day for discharge (baseline); and educational short messages through message platform once a week. Dosage and adjustment of statins, and concomitant medications in all the treated patients will be recorded.
Arm Title
Control Group
Arm Type
Sham Comparator
Arm Description
The Control Group will receive 3 visits and receive care as per usual practice by the treating doctor and a follow-up brochure without medical expert letter. Dosage and adjustment of statins, and concomitant medications in all the treated patients will be recorded. Blood lipid panel (4 items), hepato-renal functions, and creatine kinase will be examined; while, Morisky 8-item questionnaire will be used to evaluate medication compliance at outpatient visits. In addition, the occurrence of major cardiovascular events and AE/SAE will be collected during the study.
Intervention Type
Behavioral
Intervention Name(s)
Intensive Education
Intervention Description
Statin Treatment:The investigator will be suggested to increase the dose of atorvastatin according to guideline if a patient's LDL-C does not achieve target level. Patient education: Routine education at discharge. 4 education brochures will be delivered to patients. Calendar with healthy tips will be delivered to patients before discharge. A follow-up brochure with medical expert letter. A total of 24 specific short messages for ACS will be developed and sent to patients (one short message per week). Telephone follow ups will be performed according to a standard communication document. At discharge, patients will be given a brochure for future follow up.
Intervention Type
Other
Intervention Name(s)
Control
Intervention Description
Statin Treatment:The recommended dosage of atorvastatin will be adjusted at the physician's discretion. Patient education: Routine education at discharge. A follow-up brochure without medical expert letter. At discharge, patients will be given a brochure for future follow up.
Primary Outcome Measure Information:
Title
LDL-C target achieving rate
Time Frame
at Week 24 post-discharge
Secondary Outcome Measure Information:
Title
LDL-C target achieving rate
Time Frame
at Week 12 post-discharge
Title
the proportions of patients with statin persistence
Time Frame
at Week 12 post-discharge
Title
the proportions of patients with statin persistence
Time Frame
at Week 24 post-discharge
Title
statin compliance
Time Frame
at Week 12 post-discharge
Title
statin compliance
Time Frame
at Week 24 post-discharge
Title
the relationship of LDL-C target achieving rate and statin compliance
Time Frame
at Week 24 post-discharge
Title
the discontinuation reason of statin therapy
Time Frame
at Week 24 post-discharge
Title
the difference of LDL-C control rate and statin compliance
Description
To find the difference of LDL-C control rate and statin compliance between pre-specified sub-groups: PCI or non-PCI/male or female/age (≥65) or not/ having medical insurance or not/dyslipidemia history or not /MI (myocardial infarction) or UA (unstable angina)/different risk level according to TIMI/ patients for first consulting or patients with recurrence/ have received statin in the last 3 months or not.
Time Frame
at Week 24 post-discharge
Other Pre-specified Outcome Measures:
Title
the major adverse cardiovascular events
Time Frame
at 24 weeks follow up

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: The patients admitted to the hospital with a diagnosis of ACS including those for first consulting or with recurrence. The patient was prescribed atorvastatin (Lipitor®) by physicians in hospital; The age of patient enrolled will be ≥18 years old; The patient is able to understand and complete questionnaire. The patients agree to accept follow-up visits, and willing to participate in patient education courses and sign informed consent form. Exclusion Criteria: The patient has contraindications to statins, such as active hepatic disease, patient has a history of intolerance or hypersensitivity to statins or has a history of prior rhabdomyolysis on a statin. The patient who uses other statins except Lipitor® when discharged from the hospital; Cardiac function class of the patient is class IV(NYHA); The patient has a malignant tumor; The patient has a severe arrhythmia.
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Bingqing Huang
Phone
86-13816586495
Email
huang.bingqing@zs-hospital.sh.cn
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Junbo Ge, Professor
Organizational Affiliation
Fudan University
Official's Role
Principal Investigator
Facility Information:
Facility Name
Fujian Medical University Union Hospital
City
Fuzhou
State/Province
Fujian
Country
China
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Ziliang Chen, Professor
Facility Name
The 2nd affiliated hospital of harbin medical university
City
Harbin
State/Province
Heilongjiang
ZIP/Postal Code
150001
Country
China
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Bo Yu, Professor
Facility Name
Xi'an Jiaotong University College of Medicine
City
Xi'an
State/Province
Shanxi
ZIP/Postal Code
710061
Country
China
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Zhuyi Yuan, Professor
Facility Name
The Luhe Teaching Hospital of the Capital Medical University
City
Beijing
Country
China
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Jincheng Guo, Professor
Facility Name
Shanghai Zhongshan Hospital
City
Shanghai
ZIP/Postal Code
200032
Country
China
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Junbo Ge, Professor

12. IPD Sharing Statement

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Intensive Education on Lipid Management

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