Effect of Patient Education on Compliance and Cardiovascular Risk Parameters

NCT ID: NCT02096887

Last Updated: 2014-03-26

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

UNKNOWN

Clinical Phase

NA

Total Enrollment

2000 participants

Study Classification

INTERVENTIONAL

Study Start Date

2014-06-30

Study Completion Date

2016-01-31

Brief Summary

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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.

Detailed Description

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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.

Conditions

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Cardiovascular Risk Factors

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Primary Study Purpose

PREVENTION

Blinding Strategy

NONE

Study Groups

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Patient Education

Patient Education

Group Type OTHER

Patient Education

Intervention Type BEHAVIORAL

Patient Education using the following two instruments:

1. Framingham Risk Score calculator:
2. Know your numbers patient booklet

Interventions

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Patient Education

Patient Education using the following two instruments:

1. Framingham Risk Score calculator:
2. Know your numbers patient booklet

Intervention Type BEHAVIORAL

Eligibility Criteria

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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
Minimum Eligible Age

30 Years

Maximum Eligible Age

70 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

Yes

Sponsors

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Pfizer

INDUSTRY

Sponsor Role collaborator

Kuwait Institute for Medical Specialization

OTHER_GOV

Sponsor Role lead

Responsible Party

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Dr. Samia Almusallam

Director of the family medicine residency program

Responsibility Role PRINCIPAL_INVESTIGATOR

Principal Investigators

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Samia Almusallam, FRCGP

Role: PRINCIPAL_INVESTIGATOR

Kuwait Institute for Medical Specialization

Maleka M Serour, MRCGP/ INT

Role: PRINCIPAL_INVESTIGATOR

Kuwait Institute for Medical Specialization

Wafa A Rashed, FRCP

Role: PRINCIPAL_INVESTIGATOR

Ministry of Health -Mubarak Hospital- Cardiology unit

Other Identifiers

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WS964765

Identifier Type: -

Identifier Source: org_study_id

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