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Clinical Trials/NCT01316367
NCT01316367
Completed
Phase 4

Effectiveness of PRECEDE Model for Health Education on Cardiovascular Risk Reduction in Patients With Type 2 Diabetes Mellitus

Hospital Carlos III, Madrid1 site in 1 country600 target enrollmentFebruary 2003

Overview

Phase
Phase 4
Intervention
Not specified
Conditions
Type 2 Diabetes Mellitus
Sponsor
Hospital Carlos III, Madrid
Enrollment
600
Locations
1
Primary Endpoint
HbA1c level
Status
Completed
Last Updated
15 years ago

Overview

Brief Summary

BACKGROUND: Individual health education is considered to be essential in the overall care of patients with type 2 diabetes (DM2), although there is some uncertainty regarding its metabolic control benefits. There have been very few randomized studies on the effects of individual education on normal care in DM2 patients with a control group, and none of these have assessed the long-term results. Therefore, this study aims to use this design to assess the effectiveness of the PRECEDE (Predisposing, Reinforcing, Enabling, Causes in Educational Diagnosis, and Evaluation) education model in the metabolic control and the reduction of cardiovascular risk factors, in patients with type 2 diabetes.

METHODS: An open community randomized clinical trial will be carried out in 8 urban community health centers in the Northeastern Madrid (Spain). Six hundred patients with DM2 will be randomized in two groups: PRECEDE or conventional model for health promotion education. The main outcome measures is glycated hemoglobin A1C, body mass index (BMI), blood pressure, lipids and control criteria during the 2-year follow-up period.

Detailed Description

Assignment to the Health Promotion Education (HPE) will be random, three centers will use conventional HPE (the control group) and the remaining five will use PRECEDE-type HPE. Eligible patients are selected from a list of DM2 patients by each professional using random sampling, until the predetermined sample size is attained. Conventional HPE is defined according to the recommendations of the Spanish Ministry of Health National Conference on Diabetes Mellitus, and was complemented by the criteria for good care of the Madrid Primary Healthcare Service for the promotion of healthy lifestyles among adults for 2004-2007

Registry
clinicaltrials.gov
Start Date
February 2003
End Date
March 2005
Last Updated
15 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Sponsor
Hospital Carlos III, Madrid

Eligibility Criteria

Inclusion Criteria

  • Older than 30 years of age, with previously diagnosed DM2 (cardinal clinical, plus random blood glucose \> 200 mg/dl or oral glucose of \> 200 mg/dl at 2 h, twice, or plasma fasting glucose of \> 126 mg/dl on two occasions or being diagnosed previously, received specific treatment for DM2)

Exclusion Criteria

  • Gestational diabetes
  • Patients involved in clinical trials
  • Patients with life expectancy less than 1 year (according to clinical judgment)
  • Patients who refused to participate
  • Homebound patients Patients meeting criteria for inclusion and not meeting any exclusion criteria were invited to participate, and were included after accepting and signing an informed consent form.

Outcomes

Primary Outcomes

HbA1c level

Time Frame: Final (before 2 years follow-up)

Secondary Outcomes

  • Blood Pressure(Final (before 2 years follow-up))
  • Low-density lipoprotein (LDL) cholesterol(Final (before 2 years of follow-up))
  • Body Mass Index (BMI)(Final (before 2 years of follow-up)

Study Sites (1)

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