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Health Improvement Through Food and Lifestyle Intervention Based On Personalized Retail Advice (FLORA)

Primary Purpose

Metabolic Syndrome, Gut Bacteria, Personalized Nutrition

Status
Unknown status
Phase
Not Applicable
Locations
Study Type
Interventional
Intervention
Microbiota modulation diet
Sponsored by
SmartWithFood
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional supportive care trial for Metabolic Syndrome focused on measuring Metabolic syndrome, Gut microbiota, Personalized dietary advice, Food literacy

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesAccepts Healthy Volunteers

Inclusion criteria

  • Willingness to participate to the study and to sign the informed consent (Dutch)
  • Older than 18 years
  • Diagnosed with pre-metabolic syndrome (diagnosed with central obesity [waist circumference ≥80 cm for women and ≥94 cm for men] and one of the following criteria: elevated blood pressure [systolic ≥130 mm Hg, diastolic ≥85 mm Hg], raised triglycerides [>150 mg/dL], reduced HDL-cholesterol [<40 mg/dL in men, <50 mg/dL in women], or raised fasting plasma glucose [≥100 mg/dL]
  • Residing in Belgium, no travels abroad planned longer than seven consecutive days during the five-months study period
  • Willingness to follow dietary guidelines during the three-months intervention period
  • Willingness to purchase bulk groceries primarily at Colruyt Group using the Collect&Go platform during the five-months study period
  • Access to a -20-18°C freezer

Exclusion criteria

  • Chronic constipation (less than one defecation once a week)
  • Gastro-intestinal surgery within the past 3 months
  • Inflammatory bowel disease (IBD) or diverticulitis
  • Irritable bowel syndrome (IBS)
  • Any food allergy or food intolerance
  • Metabolic syndrome
  • Diabetes Mellitus Type 1 or Type 2
  • Coeliac disease
  • Pregnant women or women planning a pregnancy during the study period
  • Lactating women
  • Subjects on a specific diet (e.g. vegetarian/vegan diet, gluten-free diet, lactose-free diet, high-protein diet)
  • Subjects being treated for hypertension or high cholesterol

Sites / Locations

    Arms of the Study

    Arm 1

    Arm 2

    Arm Type

    Experimental

    No Intervention

    Arm Label

    Study arm

    Control arm

    Arm Description

    During the three months intervention period, participants within this arm will do their groceries through the online Collect&Go platform of Colruyt Group. Dietitians will adjust their shopping carts by changing food products by healthier alternative ones taking into account the Flemish food-based dietary guidelines. Based on participants' dietary pattern and level of food literacy, personalized dietary advice will be provided and a dietitian helpline will be available for further nutrition-related questions.

    During the three months intervention period, participants within this arm will do their groceries through the online Collect&Go platform of Colruyt Group. Dietitians will adjust their shopping carts by changing food products by healthier alternative ones taking into account the guidelines from the newly developed microbiota modulation diet (MMD). Based on participants' dietary pattern and level of food literacy, personalized dietary advice will be provided and a dietitian helpline will be available for further nutrition-related questions.

    Outcomes

    Primary Outcome Measures

    Reduced waist circumference
    Participants' waist circumference (cm) decreases during the study period
    Reduced serum triglycerides
    Participants' serum triglyceride level (mg/dL) decreases during the study period (blood sample analysis)
    Reduced blood pressure
    Participants' blood pressure (mm Hg) decreases during the study period
    Elevated HDL-cholesterol
    Participants' HDL-cholesterol levels (mg/dL) increase during the study period (blood sample analysis)
    Reduced fasting plasma glucose
    Participants' fasting plasma glucose levels decrease during the study period (blood sample analysis)

    Secondary Outcome Measures

    Full Information

    First Posted
    September 18, 2019
    Last Updated
    October 19, 2020
    Sponsor
    SmartWithFood
    Collaborators
    Vlaams Instituut voor Biotechnologie, KU Leuven
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    1. Study Identification

    Unique Protocol Identification Number
    NCT04102891
    Brief Title
    Health Improvement Through Food and Lifestyle Intervention Based On Personalized Retail Advice
    Acronym
    FLORA
    Official Title
    Health Improvement Through Food and Lifestyle Intervention Based On Personalized Retail Advice
    Study Type
    Interventional

    2. Study Status

    Record Verification Date
    September 2020
    Overall Recruitment Status
    Unknown status
    Study Start Date
    February 2021 (Anticipated)
    Primary Completion Date
    June 2021 (Anticipated)
    Study Completion Date
    July 2021 (Anticipated)

    3. Sponsor/Collaborators

    Responsible Party, by Official Title
    Sponsor
    Name of the Sponsor
    SmartWithFood
    Collaborators
    Vlaams Instituut voor Biotechnologie, KU Leuven

    4. Oversight

    Studies a U.S. FDA-regulated Drug Product
    No
    Studies a U.S. FDA-regulated Device Product
    No
    Data Monitoring Committee
    No

    5. Study Description

    Brief Summary
    FLORA is a longitudinal intervention study with a randomized, parallel group design. Primary objective is to improve metabolic health through gut microbiota modulation by means of a retailer-driven personalized dietary intervention in a real-life setting. Four hundred Flemish pre-metabolic adults will be randomly divided into a control and treatment arm, each comprising 200 participants. The study period is divided into three phases: a four weeks characterization, a twelve weeks intervention, and a four weeks post-intervention phase. During the intervention phase, control participants' online Collect&Go shopping carts are adjusted in accordance with Flemish food-based dietary guidelines. Based on the same guidelines, participants are provided with personalized dietary advice considering their usual dietary pattern and level of food literacy. In the treatment arm, a similar intervention will be applied using guidelines based on a microbiota modulation diet (MMD). During intervention, all participants can contact a dietician helpline for additional advice on study-related dietary issues. Over the five months, saliva and fecal samples will be collected on a regular basis, with an intensive sampling period of seven consecutive days at the end of each study phase. A GP consult consisting of a short medical exam, blood withdrawal and medical questionnaire takes place each month. Further, online questionnaires on lifestyle, health and well-being will be sent by e-mail and each five days, participants complete a food diary through their smartphone. Fecal, saliva, blood samples and meta-data will be analysed to detect changes in metabolic health.

    6. Conditions and Keywords

    Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
    Metabolic Syndrome, Gut Bacteria, Personalized Nutrition
    Keywords
    Metabolic syndrome, Gut microbiota, Personalized dietary advice, Food literacy

    7. Study Design

    Primary Purpose
    Supportive Care
    Study Phase
    Not Applicable
    Interventional Study Model
    Parallel Assignment
    Masking
    Participant
    Allocation
    Randomized
    Enrollment
    400 (Anticipated)

    8. Arms, Groups, and Interventions

    Arm Title
    Study arm
    Arm Type
    Experimental
    Arm Description
    During the three months intervention period, participants within this arm will do their groceries through the online Collect&Go platform of Colruyt Group. Dietitians will adjust their shopping carts by changing food products by healthier alternative ones taking into account the Flemish food-based dietary guidelines. Based on participants' dietary pattern and level of food literacy, personalized dietary advice will be provided and a dietitian helpline will be available for further nutrition-related questions.
    Arm Title
    Control arm
    Arm Type
    No Intervention
    Arm Description
    During the three months intervention period, participants within this arm will do their groceries through the online Collect&Go platform of Colruyt Group. Dietitians will adjust their shopping carts by changing food products by healthier alternative ones taking into account the guidelines from the newly developed microbiota modulation diet (MMD). Based on participants' dietary pattern and level of food literacy, personalized dietary advice will be provided and a dietitian helpline will be available for further nutrition-related questions.
    Intervention Type
    Other
    Intervention Name(s)
    Microbiota modulation diet
    Intervention Description
    The Collect&Go shopping carts of the 400 participants will be adapted by replacing food products by healthier alternative ones based on the Flemish food-based dietary guidelines and the microbiota modulation diet guidelines for the control and study arm respectively. Based on these guidelines, and the habitual dietary pattern and level of food literacy of the participant, personalized dietary advice will be provided. A dietitian helpline will be available for further nutritional issues as well.
    Primary Outcome Measure Information:
    Title
    Reduced waist circumference
    Description
    Participants' waist circumference (cm) decreases during the study period
    Time Frame
    5 months
    Title
    Reduced serum triglycerides
    Description
    Participants' serum triglyceride level (mg/dL) decreases during the study period (blood sample analysis)
    Time Frame
    5 months
    Title
    Reduced blood pressure
    Description
    Participants' blood pressure (mm Hg) decreases during the study period
    Time Frame
    5 months
    Title
    Elevated HDL-cholesterol
    Description
    Participants' HDL-cholesterol levels (mg/dL) increase during the study period (blood sample analysis)
    Time Frame
    5 months
    Title
    Reduced fasting plasma glucose
    Description
    Participants' fasting plasma glucose levels decrease during the study period (blood sample analysis)
    Time Frame
    5 months

    10. Eligibility

    Sex
    All
    Minimum Age & Unit of Time
    18 Years
    Accepts Healthy Volunteers
    Accepts Healthy Volunteers
    Eligibility Criteria
    Inclusion criteria Willingness to participate to the study and to sign the informed consent (Dutch) Older than 18 years Diagnosed with pre-metabolic syndrome (diagnosed with central obesity [waist circumference ≥80 cm for women and ≥94 cm for men] and one of the following criteria: elevated blood pressure [systolic ≥130 mm Hg, diastolic ≥85 mm Hg], raised triglycerides [>150 mg/dL], reduced HDL-cholesterol [<40 mg/dL in men, <50 mg/dL in women], or raised fasting plasma glucose [≥100 mg/dL] Residing in Belgium, no travels abroad planned longer than seven consecutive days during the five-months study period Willingness to follow dietary guidelines during the three-months intervention period Willingness to purchase bulk groceries primarily at Colruyt Group using the Collect&Go platform during the five-months study period Access to a -20-18°C freezer Exclusion criteria Chronic constipation (less than one defecation once a week) Gastro-intestinal surgery within the past 3 months Inflammatory bowel disease (IBD) or diverticulitis Irritable bowel syndrome (IBS) Any food allergy or food intolerance Metabolic syndrome Diabetes Mellitus Type 1 or Type 2 Coeliac disease Pregnant women or women planning a pregnancy during the study period Lactating women Subjects on a specific diet (e.g. vegetarian/vegan diet, gluten-free diet, lactose-free diet, high-protein diet) Subjects being treated for hypertension or high cholesterol

    12. IPD Sharing Statement

    Plan to Share IPD
    No

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