Educational Intervention Targeting Statin Therapy and Compliance in Diabetic Patients

NCT ID: NCT04499846

Last Updated: 2021-10-13

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

COMPLETED

Total Enrollment

96 participants

Study Classification

OBSERVATIONAL

Study Start Date

2020-06-11

Study Completion Date

2021-05-07

Brief Summary

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The objective of the study is to measure changes in compliance to statin therapy in patients with type 2 diabetes after an educational intervention. This intervention is part of the therapeutic education of the diabetic patient, carried out throughout the follow-up of his/her diabetes.

Detailed Description

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Conditions

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Type II Diabetes

Study Design

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Observational Model Type

CASE_ONLY

Study Time Perspective

PROSPECTIVE

Study Groups

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Diabetic patients following education

Patients will followed an educational intervention about physiopathology of diabetes and mechanisms of action of statins. A questionnaire will allow to measure compliance to the treatment.

Therapeutic education

Intervention Type OTHER

Patients will follow a therapeutic education in order to inform them about the mechanism of action of statins. After this intervention a questionnaire will use to measure compliance.

Interventions

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Therapeutic education

Patients will follow a therapeutic education in order to inform them about the mechanism of action of statins. After this intervention a questionnaire will use to measure compliance.

Intervention Type OTHER

Eligibility Criteria

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Inclusion Criteria

* 18 years old or more
* Type 2 diabetes
* Following treatment with statins
* Hospitalization in the diabetes day hospitals of the Saint Philibert or Saint Vincent Hospitals (Lille, France).
* Ability to answer the Girerd test in both interviews (in the individual interview and by phone)
* Patient informed to participate in the study
* Signed patient's consent.

Exclusion Criteria

* Patients under guardianship
Minimum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Lille Catholic University

OTHER

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Principal Investigators

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François Delecourt, MD

Role: PRINCIPAL_INVESTIGATOR

GHICL

Locations

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Hôpital Saint-philibert

Lomme, Hauts-de-France, France

Site Status

Countries

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France

Other Identifiers

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2020-A00402-37

Identifier Type: OTHER

Identifier Source: secondary_id

RC-P0096

Identifier Type: -

Identifier Source: org_study_id