NCT04522258

Brief Summary

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

Trial Health

87
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
70

participants targeted

Target at P50-P75 for not_applicable

Timeline
Completed

Started May 2019

Geographic Reach
1 country

1 active site

Status
completed

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Start

First participant enrolled

May 2, 2019

Completed
1.2 years until next milestone

First Submitted

Initial submission to the registry

July 14, 2020

Completed
1 month until next milestone

First Posted

Study publicly available on registry

August 21, 2020

Completed
3 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

November 8, 2020

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

November 8, 2020

Completed
Last Updated

January 7, 2021

Status Verified

January 1, 2021

Enrollment Period

1.5 years

First QC Date

July 14, 2020

Last Update Submit

January 6, 2021

Conditions

Outcome Measures

Primary Outcomes (1)

  • Stress sensitivity (cortisol)

    Induction of cognitive, physical, and social stress using Maastricht Acute Stress Test. Stress hormone cortisol is quantified by gathering multiple saliva samples throughout the stress induction and recovery during both pre-intervention and post-intervention visit.

    through study completion, on average 1 year and 5 months

Secondary Outcomes (13)

  • Stress sensitivity (subjective)

    through study completion, on average 1 year and 5 months

  • Cortisol awakening response

    through study completion, on average 1 year and 5 months

  • Fear

    through study completion, on average 1 year and 5 months

  • Fear (subjective)

    through study completion, on average 1 year and 5 months

  • Positive and Negative Affect Schedule (PANAS)

    through study completion, on average 1 year and 5 months

  • +8 more secondary outcomes

Study Arms (2)

Placebo

PLACEBO COMPARATOR

Refined cereal flour

Dietary Supplement: Placebo

Dietary fiber

ACTIVE COMPARATOR

Fermentable cereal bran

Dietary Supplement: Dietary fiber

Interventions

Dietary fiberDIETARY_SUPPLEMENT

Fermentable cereal bran

Dietary fiber
PlaceboDIETARY_SUPPLEMENT

Refined cereal flour

Placebo

Eligibility Criteria

Age20 Years - 40 Years
Sexmale
Healthy VolunteersYes
Age GroupsAdult (18-64)

You may qualify if:

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

You may not qualify if:

  • 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

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

UZ Leuven/Stresslab

Leuven, I Am Not in the U.S. Or Canada, 3000, Belgium

Location

MeSH Terms

Interventions

Dietary Fiber

Intervention Hierarchy (Ancestors)

Dietary CarbohydratesCarbohydratesFoodDiet, Food, and NutritionPhysiological PhenomenaFood and Beverages

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
TRIPLE
Who Masked
PARTICIPANT, INVESTIGATOR, OUTCOMES ASSESSOR
Masking Details
Participants, investigators, and personnel involved in data analyses are blinded to the intervention. Unblinding occurs after all data has been collected AND analysed.
Purpose
BASIC SCIENCE
Intervention Model
PARALLEL
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Prof. Dr. Kristin Verbeke

Study Record Dates

First Submitted

July 14, 2020

First Posted

August 21, 2020

Study Start

May 2, 2019

Primary Completion

November 8, 2020

Study Completion

November 8, 2020

Last Updated

January 7, 2021

Record last verified: 2021-01

Locations