Stimulating Fiber Intake Via Personalized Dietary Advice
- Conditions
- Personalized AdviceMicrobiotaDietary FiberDietary Habits
- Interventions
- Other: Control (no intervention)Behavioral: PDA
- Registration Number
- NCT03848546
- Lead Sponsor
- Wageningen University
- Brief Summary
Dietary fibers are linked to improved health and prevention of diseases such as obesity, stroke, hypertension, diabetes and colorectal cancer. Moreover, fibers play a crucial role in improving and maintaining gut health, by increasing stool weight,stool frequency and improvement of stool consistency. Currently, very few adults meet the recommendation of 30 (females) or 40 (males) grams per day. Personalized dietary advice may be the solution to increase dietary fiber intake in large populations.
The objective is to investigate if a personalized dietary advice is more effective in increasing dietary fiber intake in the Dutch population than the general advice that is currently provided by the Netherlands Nutrition center and the Dutch Digestive Foundation (MLDS).Second objective is to assess the effect of increased fiber intake on stool pattern, perceived well-being and consumer behavior parameters and the role of psychological factors in the effectiveness of personalized dietary advice on dietary fiber intake.
Study design: A 4.5-month (6 weeks intervention + follow-up after 3 months) single-blind randomized controlled trial with two groups: the intervention group, which receives personalized dietary advice (PDA), and the control group, which only receives the general dietary advice. Primary study parameters/outcome of the study: Primary endpoint is dietary fiber intake, which will be assessed using an Food Frequency Questionnaire and 24hr recalls.
Fecal microbiota composition and metabolite levels will be used as an objective marker for fiber intake. Secondary study parameters/outcome of the study (if applicable):
Secondary parameters include stool pattern, well-being, hunger, satiety and body weight. Furthermore, psychological measurements will give insight into why the PDA was (not) effective.
- Detailed Description
This study is performed in healthy adults, older than 18 years, with no gastro-intestinal complaints. The intervention group receives personalized dietary advice (PDA) based on their current food pattern, preferences and selfregulation capacity. The PDA aims to compute high-fiber alternatives for products that subjects currently use and that are close to their current eating behavior, to help increase dietary fiber intake. This PDA will be provided using an online webportal. The control group only receives a general dietary advice, e.g. (a) flyer(s) containing information on fibers from the Netherlands Nutrition Center and the MLDS. The intervention group will also receive this general advice next to the PDA.
Recruitment & Eligibility
- Status
- COMPLETED
- Sex
- All
- Target Recruitment
- 106
-
Age ≥18 years.
-
Apparently healthy: no gastrointestinal complaints, no food allergies and no medication that can influence the outcome of the study (see exclusion criteria).
-
Relatively low fiber intake: which is assessed by a short fiber intake screening questionnaire (score ranging from
1 to 22). Females with a score ≤13 and males with a score ≤15 will be included in the study.
-
Living in the surroundings of Wageningen (max. 50 km).
-
In possession of a mobile phone with android ≥4.4 or iOS system ≥9 to use apps.
-
Signed informed consent.
- Any digestive tract disorder that is expected to interfere with the study outcomes, such as chronic constipation or diarrhea, Crohn's Disease, Ulcerative Colitis, Irritable Bowel Syndrome, Coeliac disease.
- Diagnosis of Diabetes Mellitus, since the change in carbohydrate intake may interfere with medication usage.
- Currently following a strict diet and unwilling or unable to change; for example a gluten free diet or a "crash diet" using meal substitutes.
- Use of medication that can interfere with the study outcomes, including laxatives, diuretics, antidepressants, codeine, antibiotics or fiber supplements
- Female subjects: currently pregnant or breastfeeding, or intending to become pregnant during the study, as this can affect stool patterns and well-being.
- Simultaneously participating in another study.
- Unwilling or unable to fulfill the study criteria.
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- PARALLEL
- Arm && Interventions
Group Intervention Description Control Control (no intervention) Receives the general advice (two flyers containing information about fiber intake) PDA PDA Intervention group: receives the personalized dietary advice
- Primary Outcome Measures
Name Time Method change in Microbiota composition Before study, at 3 weeks and at 6 weeks of a fecal sample
Change in dietary fiber intake Before study, after 6 weeks intervention, and 3 months follow-up Will be measured using the Food Frequency Questionnaire, and 24hr recalls to compute grams of fiber.
change in Short Chain Fatty acid level Before study, at 3 weeks and at 6 weeks of a fecal sample
- Secondary Outcome Measures
Name Time Method Stool pattern Daily during 6-week intervention Bristol stool chart en stool frequency
Body weight study start, and after 6 weeks Subjects weigh themselves (morning, fasted)
Hunger and Satiety Daily during 6-week intervention Using validated questions
Perceived wellbeing Daily during 6-week intervention Using validated questions
Psychological questionnaires Before and after the 6-week intervention, and at 3-months follow-up Validated questionnaire will be used to assess motives, barriers, knowledge, intentions, self-efficacy, self-regulation and knowledge
Trial Locations
- Locations (1)
Wageningen University, Division of Human Nutrition
🇳🇱Wageningen, Netherlands