Evaluation of Nutritional Prevention Program for Women's Cardiovascular Health on Quality of Life (SAFE)
NCT ID: NCT06380218
Last Updated: 2024-04-23
Study Results
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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RECRUITING
NA
50 participants
INTERVENTIONAL
2023-07-11
2025-08-01
Brief Summary
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Detailed Description
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The nutritional prevention program includes tools and 10 collective workshops to change the life behaviours (eating habits and physical activity) by assessing :
* Food balance and diversity
* Eating behaviour and representations
* Level of knowledge in nutrition
* Level of physical activity and physical inactivity
* Physical abilities: strength, balance, flexibility, cardio respiratory endurance, recovery capacity
* Behavioural barriers and educational levers to improve women's cardiovascular health
Conditions
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Study Design
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NA
SINGLE_GROUP
PREVENTION
NONE
Study Groups
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Nutrional and physical activity program
10 collective combined workshops of nutrition and physical activity = 1 per week during 10 weeks associated to margarine consumption
Nutrional and physical activity program
Nutritional prevention and physical activity workshops associated with a substitution of saturated and/or trans fatty acids by cis-unsaturated acids via the consumption of Primevère margarine to influence lifestyle habits, quality of life and improvement of the lipid profile of women with cardiovascular risk
Interventions
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Nutrional and physical activity program
Nutritional prevention and physical activity workshops associated with a substitution of saturated and/or trans fatty acids by cis-unsaturated acids via the consumption of Primevère margarine to influence lifestyle habits, quality of life and improvement of the lipid profile of women with cardiovascular risk
Eligibility Criteria
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Inclusion Criteria
* Regularly consuming butter and/or "standard" margarine rich in saturated fatty acids
Exclusion Criteria
* Consuming omega-3 rich food supplements within 3 months of inclusion
* Treated with lipid-lowering agents (statins), antidiabetic or antihypertensive drugs for less than 3 months
* Suffering of eating disorders
* Presenting a medical contraindication to the practice of physical activity
* Having previously participated in a similar prevention program
* Suffering from serious chronic diseases (cancer, serious cardiovascular history, etc.)
40 Years
65 Years
FEMALE
Yes
Sponsors
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Institut Pasteur de Lille
OTHER
Responsible Party
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Jean-Michel Lecerf
Principal Invesigator
Principal Investigators
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Jean-Michel Lecerf, MD
Role: PRINCIPAL_INVESTIGATOR
Institut Pasteur de Lille - NutrInvest
Locations
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NutrInvest - Institut Pasteur de Lille
Lille, Nord, France
Countries
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Central Contacts
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Facility Contacts
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Other Identifiers
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2023-A00249-36
Identifier Type: -
Identifier Source: org_study_id
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