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Clinical Trial Details — Status: Not yet recruiting

Administrative data

NCT number NCT02096887
Other study ID # WS964765
Secondary ID
Status Not yet recruiting
Phase N/A
First received March 24, 2014
Last updated March 25, 2014
Start date June 2014
Est. completion date January 2016

Study information

Verified date March 2014
Source Kuwait Institute for Medical Specialization
Contact n/a
Is FDA regulated No
Health authority Kuwait: Joint Committee for the Protection of Human Subjects in Research
Study type Interventional

Clinical Trial Summary

Patient's awareness of their risk factors for heart disease and their active involvement in their own management plan can help improve their adherence to treatment and their risk profile. The purpose of this study is to investigate the influence of patient education and awareness of heart disease risk factors on compliance to medication and lifestyle modification.


Description:

Prospective cluster randomized interventional study with primary health care clinics as clusters.Clinics will be randomized to conventional care or to structured patient education in addition to care. Trained physicians will extract information from the patient medical record and will conduct a personal interview with the participants, after they finish with their routine visit, to fill a case report form (CRF)

CRF will include the following items:

- Patient Demographics,

- Socioeconomic: income, employment and education

- Past Medical History

- Smoking history

- Alcohol use

- Medications

- Adherence: Morisky scale

- Examination: BP, weight, height, waist

- Investigations: LDL-C, HbA1C 2.Compliance/adherence to the medication will be measured by using the Morisky scale, which is a validated scale for measuring adherence in hypertension and diabetic patients among other disease.

Patients attending clinics that are randomized to structured patient education will receive education targeting all the risk factors they have. They will be informed about specific evidence -based target values they should achieve for each of the risk factors. Their compliance to prescribed medications will be encouraged and specific advice about improving compliance will be given. To achieve this physicians in the education clinics are going to use two items:

1. Framingham Risk Score calculator.

2. Know your numbers patient booklet.

Follow up visits will be scheduled at 2 months, 6 months and 12 months after the initial visit. For patients in both education and conventional clinics, compliance to medications will be assessed and the degree of risk factor control will also be determined through specific measurements that include number of cigarettes smoked, systolic and diastolic blood pressure, body mass index and waist circumference, HBA1C and LDL values.


Recruitment information / eligibility

Status Not yet recruiting
Enrollment 2000
Est. completion date January 2016
Est. primary completion date January 2015
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Both
Age group 30 Years to 70 Years
Eligibility Inclusion Criteria:

- Patients with one or more CVD risk factors will be consecutively enrolled, smokers and obese patients should have an additional risk factors

- The risk factors are based on Framingham Risk Score calculator and include smoking, high blood pressure, high blood cholesterol ,diabetes and being overweight or obese

- All participants must be adults (30 -70 years of age) who give an informed consent

- All participants should be of Kuwaity nationality, literate and fluent in either Arabic or English

- Patients are likely to be available for a one year follow up

Exclusion Criteria:

- Patients with mental disability or severe psychiatric disorder who are unable to provide informed consent or participate in educational activities.

- Patients with severe visual or hearing disability that will prevent participation in the educational activity

- Patients <30 years or >70 years of age

- Illiterate patients

- Non Kuwaity nationals

- Patients who are not permanently resident in Kuwait

- Patient who refuse to provide the informed consent

Study Design

Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Prevention


Related Conditions & MeSH terms


Intervention

Behavioral:
Patient Education
Patient Education using the following two instruments: Framingham Risk Score calculator: Know your numbers patient booklet

Locations

Country Name City State
n/a

Sponsors (2)

Lead Sponsor Collaborator
Kuwait Institute for Medical Specialization Pfizer

Outcome

Type Measure Description Time frame Safety issue
Primary cardiovascualr risk factor control Cardiovascular risk factors control as assessed by the following parameters: HbA1C, Blood pressure, LDL-C, BMI and smoking cessation 12 months No
Primary medication compliance Medication compliance as assessed by Morisky scale 12 months No
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