Effects of Dietary Fiber on Affective Processes
1 other identifier
interventional
70
1 country
1
Brief Summary
The effects of dietary fiber on psychobiological processes are examined in a sample of healthy volunteers.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P50-P75 for not_applicable
Started May 2019
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
Study Start
First participant enrolled
May 2, 2019
CompletedFirst Submitted
Initial submission to the registry
July 14, 2020
CompletedFirst Posted
Study publicly available on registry
August 21, 2020
CompletedPrimary Completion
Last participant's last visit for primary outcome
November 8, 2020
CompletedStudy Completion
Last participant's last visit for all outcomes
November 8, 2020
CompletedJanuary 7, 2021
January 1, 2021
1.5 years
July 14, 2020
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 COMPARATORRefined cereal flour
Dietary fiber
ACTIVE COMPARATORFermentable cereal bran
Interventions
Eligibility Criteria
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
- KU Leuvenlead
Study Sites (1)
UZ Leuven/Stresslab
Leuven, I Am Not in the U.S. Or Canada, 3000, Belgium
MeSH Terms
Interventions
Intervention Hierarchy (Ancestors)
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