Effects of Dietary Fiber on Affective Processes

NCT ID: NCT04522258

Last Updated: 2021-01-07

Study Results

Results pending

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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Recruitment Status

COMPLETED

Clinical Phase

NA

Total Enrollment

70 participants

Study Classification

INTERVENTIONAL

Study Start Date

2019-05-02

Study Completion Date

2020-11-08

Brief Summary

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The effects of dietary fiber on psychobiological processes are examined in a sample of healthy volunteers.

Detailed Description

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The study is an interventional triple-blind, placebo-controlled, parallel group design with 2 arms (placebo, dietary fiber). Healthy male participants adhere to their normal eating habits for the duration of the study (32 days). At the baseline study visit, measurements are taken in the lab, including biological samples and psychophysiological measurements. Participants then consume placebo or dietary fiber for 4 weeks and revisit the lab on day 32 for a second measurement of the outcomes of interest. Specifically, we investigate the effect of dietary fiber on affective processing, including stress sensitivity and fear-related processes (e.g. extinction learning). Volunteers also respond to questionnaires in relation to mood and GI symptoms, and provide biological samples (saliva, blood, faecal, and urine samples) for analysis of cortisol levels, circulating short chain fatty acids and serum BDNF, faecal SCFA and microbiota composition, and intestinal permeability, respectively.

Conditions

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Emotions Stress Fear

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Primary Study Purpose

BASIC_SCIENCE

Blinding Strategy

TRIPLE

Participants Investigators Outcome Assessors
Participants, investigators, and personnel involved in data analyses are blinded to the intervention. Unblinding occurs after all data has been collected AND analysed.

Study Groups

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Placebo

Refined cereal flour

Group Type PLACEBO_COMPARATOR

Placebo

Intervention Type DIETARY_SUPPLEMENT

Refined cereal flour

Dietary fiber

Fermentable cereal bran

Group Type ACTIVE_COMPARATOR

Dietary fiber

Intervention Type DIETARY_SUPPLEMENT

Fermentable cereal bran

Interventions

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Dietary fiber

Fermentable cereal bran

Intervention Type DIETARY_SUPPLEMENT

Placebo

Refined cereal flour

Intervention Type DIETARY_SUPPLEMENT

Eligibility Criteria

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Inclusion Criteria

* Male participants
* Age range 20-40 years
* BMI range 18.5-27
* Dutch or English as native-language

Exclusion Criteria

* previous or current neurological, psychiatric, gastrointestinal or endocrine disorders, or other relevant medical history
* current or recent regular medication use
* previous or current substance/alcohol dependence or abuse (\> 2 units per day/14 units per week)
* one or more diagnoses based on the mini-international neuropsychiatric interview
* smoking
* night-shift work
* adherence to vegan or vegetarian diets
* use of pre- or probiotics within one month preceding the study
* use of antibiotics within 3 months preceding the study
* Habitual diet not exceeding consumption of 25 g of dietary fiber per day
* previous experience with one of the tasks used in the study
Minimum Eligible Age

20 Years

Maximum Eligible Age

40 Years

Eligible Sex

MALE

Accepts Healthy Volunteers

Yes

Sponsors

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KU Leuven

OTHER

Sponsor Role lead

Responsible Party

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Kristin Verbeke

Prof. Dr. Kristin Verbeke

Responsibility Role PRINCIPAL_INVESTIGATOR

Locations

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UZ Leuven/Stresslab

Leuven, I Am Not in the U.S. Or Canada, Belgium

Site Status

Countries

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Belgium

Other Identifiers

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S62344

Identifier Type: -

Identifier Source: org_study_id

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