Cardiovascular Risk Factors And Intensive Dietary Counselling
Primary Purpose
High Blood Pressure, Hypercholesterolemia, Tobacco Smoking
Status
Unknown status
Phase
Not Applicable
Locations
Study Type
Interventional
Intervention
Group-level Intensive dietary Counselling
Individual-level Intensive Dietary Counselling
Sponsored by

About this trial
This is an interventional prevention trial for High Blood Pressure focused on measuring Cardiovascular risk, Primary prevention, Intensive dietary counselling, Physical exercise
Eligibility Criteria
Inclusion Criteria:
- Age between 40-65 years
- Presence of any cardiovascular risk factors (Hypertension, Hypercholesterolemia, tobacco smoking, diabetes, obesity)
Exclusion Criteria:
- Currently diagnosed with any vardiovascular disease
- Currently involved in any other clinical trial
- Cognitive impairment that prevents from providing an informed consent
Sites / Locations
Arms of the Study
Arm 1
Arm 2
Arm Type
Experimental
Active Comparator
Arm Label
Group-level Intensive Dietary Counselling
Individual-level Intensive Dietary Counselling
Arm Description
Active learning through 4-6 60-minute sessions workshop, enrolling 8-12 people each time.
Individualised dietary counselling delivered at the health-care point
Outcomes
Primary Outcome Measures
Cardiovascular risk as calculated by means of the SCORE (Systematic Coronary Risk Evaluation) scale. Low-risk regions version.
Secondary Outcome Measures
Health-Related Quality of Life
Spanish version of the EQ-5D-5L questionnaire by the EuroQol Group
Full Information
NCT ID
NCT02173600
First Posted
June 24, 2014
Last Updated
June 24, 2014
Sponsor
Andalusian Regional Ministry of Health
Collaborators
Andaluz Health Service
1. Study Identification
Unique Protocol Identification Number
NCT02173600
Brief Title
Cardiovascular Risk Factors And Intensive Dietary Counselling
Official Title
Estimation of Cardiovascular Risk After Intensive Dietary Counselling in a Primary Care Setting
Study Type
Interventional
2. Study Status
Record Verification Date
June 2014
Overall Recruitment Status
Unknown status
Study Start Date
May 2014 (undefined)
Primary Completion Date
June 2015 (Anticipated)
Study Completion Date
December 2015 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Andalusian Regional Ministry of Health
Collaborators
Andaluz Health Service
4. Oversight
Data Monitoring Committee
Yes
5. Study Description
Brief Summary
The Intensive Dietary Counselling (IDC) intervention is a prevention and health promotion activity. It is being implemented by the Andalusian Health Service to reinforce basic intervention advice on healthy diet and exercise. The IDC intervention is aimed at the prevention of diseases of the heart and blood vessels (e.g. heart failure, heart attack and stroke).
The main objective of the present study is to assess adherence to the IDC intervention and, consequently, its effectiveness on the prevention of the above mentioned diseases.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
High Blood Pressure, Hypercholesterolemia, Tobacco Smoking
Keywords
Cardiovascular risk, Primary prevention, Intensive dietary counselling, Physical exercise
7. Study Design
Primary Purpose
Prevention
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
Investigator
Allocation
Randomized
Enrollment
630 (Anticipated)
8. Arms, Groups, and Interventions
Arm Title
Group-level Intensive Dietary Counselling
Arm Type
Experimental
Arm Description
Active learning through 4-6 60-minute sessions workshop, enrolling 8-12 people each time.
Arm Title
Individual-level Intensive Dietary Counselling
Arm Type
Active Comparator
Arm Description
Individualised dietary counselling delivered at the health-care point
Intervention Type
Behavioral
Intervention Name(s)
Group-level Intensive dietary Counselling
Intervention Type
Behavioral
Intervention Name(s)
Individual-level Intensive Dietary Counselling
Primary Outcome Measure Information:
Title
Cardiovascular risk as calculated by means of the SCORE (Systematic Coronary Risk Evaluation) scale. Low-risk regions version.
Time Frame
upt to 12 months from the beginning
Secondary Outcome Measure Information:
Title
Health-Related Quality of Life
Description
Spanish version of the EQ-5D-5L questionnaire by the EuroQol Group
Time Frame
Baseline, 6 and 12 months from the beginning
Other Pre-specified Outcome Measures:
Title
Chronic low-grade inflammation
Description
High sensibility c-reactive protein
Time Frame
Baseline, 6 and 12 months from the beginning
10. Eligibility
Sex
All
Minimum Age & Unit of Time
40 Years
Maximum Age & Unit of Time
65 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria:
Age between 40-65 years
Presence of any cardiovascular risk factors (Hypertension, Hypercholesterolemia, tobacco smoking, diabetes, obesity)
Exclusion Criteria:
Currently diagnosed with any vardiovascular disease
Currently involved in any other clinical trial
Cognitive impairment that prevents from providing an informed consent
12. IPD Sharing Statement
Learn more about this trial
Cardiovascular Risk Factors And Intensive Dietary Counselling
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