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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT02140658
Other study ID # TTYY20140312
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date May 2014
Est. completion date September 2015

Study information

Verified date December 2018
Source Ministry of Science and Technology of the People´s Republic of China
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The purpose of this study is to assess the affect of multiple health education interventions for statins medication Persistence and clinical prognosis of ischemic stroke patients at 3, 6 and 12 months.


Description:

The study is a prospective, multicenter, hospital-based study on secondary prevention for patients with ischemic cerebrovascular diseases between May 2014 and June 2015. Physicians from 24 hospitals in Beijing underwent a standard secondary prevention training of ischemic cerebrovascular diseases by professional training, instruction manuals, stratification management software. In order to improve the persistence of taking preventive secondary medicine, IS patients from these 24 hospitals received healthy education through manuals and Digital Video Disc about health education during hospitalization and acquired secondary preventive knowledge of ischemic cerebrovascular diseases through regular health education messages during 6 months after discharge. Patients with IS from other 6 hospitals were used as a control, and no such intervention was given to them.

Telephone follow-up was performed at 3 months, 6 months, and 1 year after the onset of cerebral infarction, during which the use of antiplatelet and statins drugs and recurrence of IS were recorded. Patients who took antiplatelet drugs or statins at three follow-ups were regarded as persistent antiplatelet drugs or statins taking within one year after the onset of the disease. The main prognostic indicator was the recurrence of IS and persistence of statins medication within 1 year, and the main purpose was to explore the impact of persistent statins use on IS recurrence.


Recruitment information / eligibility

Status Completed
Enrollment 3111
Est. completion date September 2015
Est. primary completion date June 2015
Accepts healthy volunteers No
Gender All
Age group 18 Years to 80 Years
Eligibility Inclusion Criteria:

1. Adult subjects (male or female =18 years);

2. Acute ischemic stroke occured within 14 days of symptoms onset

3. Blood low density lipoprotein (LDL) ?100mg/dl(2.59mmol/L)

4. Patients were prescribed statins at discharge

5. Patients signed informed consent

6. Patients have a cell phone and have the ability to receive and view messages

Exclusion Criteria:

1. Non-cerebrovascular events or hemorrhagic stroke

2. Patients have serious heart, liver, kidney dysfunction or coagulation disorders

3. Patients have circumstances that may affect the follow-up such as disturbance of consciousness, severe depression or other mental disorders, aphasia

4. Modified Rankin Scale score at discharge =3

5. Patients with severe vision or vision field impairment which may affect patients to read message in cell phone

6. Those who are participating in other clinical trials

7. Those who can not guarantee with the completion of 6 month follow-up after enrollment

Study Design


Related Conditions & MeSH terms


Intervention

Behavioral:
multiple health education interventions

conventional health education


Locations

Country Name City State
China Beijing Tian Tan Hospital, Capital Medical University Beijing

Sponsors (2)

Lead Sponsor Collaborator
yongjun wang Ministry of Science and Technology of the People´s Republic of China

Country where clinical trial is conducted

China, 

Outcome

Type Measure Description Time frame Safety issue
Primary Proportion of patients who continued taking statins drugs at three months after stroke onset. Statins Medication persistence at 3 months. Patients who took statins at three months follow-up were regarded as persistent during three months. 3 months after stroke onset
Primary Proportion of patients who continued taking statins drugs at six months after stroke onset. Statins Medication persistence at 6 months.Patients who took statins at six months follow-up were regarded as persistent at six months. 6 months after stroke onset
Primary Proportion of patients who continued taking statins drugs at 12 months after stroke onset. Statins Medication persistence at 12 months.Patients who took statins at twelve months follow-up were regarded as persistent at twelve months. 12 months after stroke onset
Primary Proportion of patients who continued taking statins drugs in 1 year after stroke onset. Statins Medication persistence in 1 year: Patients who took statins at 3, 6 and 12 months follow-up were regarded as persistent during one year after stroke onset. 1 year after stroke onset
Primary Recurrence of ischemic stroke in three months after stroke onset Recurrence of ischemic stroke was defined as a new focal neurological deficit of vascular origin lasting >24 hours and without hemorrhage on computed tomography or MRI of the brain. 3 months after stroke onset
Primary Recurrence of ischemic stroke in six months after stroke onset Recurrence of ischemic stroke was defined as a new focal neurological deficit of vascular origin lasting >24 hours and without hemorrhage on computed tomography or MRI of the brain. 6 months after stroke onset
Primary Recurrence of ischemic stroke in 12 months after stroke onset Recurrence of ischemic stroke was defined as a new focal neurological deficit of vascular origin lasting >24 hours and without hemorrhage on computed tomography or MRI of the brain. 12 months after stroke onset
Secondary Percentage of patients with 3-month poor clinical prognosis (including Death or Nonfatal myocardial infarction or Nonfatal hemorrhagic stroke or Severe disabilities) as a cluster and evaluated individually Death included Vascular death and non-vascular death; Severe disabilities was defined as modified Rankin Scale =4 3 months after stroke onset
Secondary Percentage of patients with 6-month poor clinical prognosis (including Death or Nonfatal myocardial infarction or Nonfatal hemorrhagic stroke or Severe disabilities) as a cluster and evaluated individually Death included Vascular death and non-vascular death; Severe disabilities was defined as modified Rankin Scale =4 6 months after stroke onset
Secondary Percentage of patients with 12-month poor clinical prognosis (including Death or Nonfatal myocardial infarction or Nonfatal hemorrhagic stroke or Severe disabilities) as a cluster and evaluated individually Death included Vascular death and non-vascular death; Severe disabilities was defined as modified Rankin Scale =4 12 months after stroke onset
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