Actively Recruiting

Phase Not Applicable
Age: 18Years - 70Years
All Genders
NCT05808036

Efficacy of the DOMINO Diet App in IBS

Led by Universitaire Ziekenhuizen KU Leuven · Updated on 2026-03-19

110

Participants Needed

1

Research Sites

174 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

The aim of this study is to evaluate whether the DOMINO diet application is an effective tool in the treatment of Irritable bowel syndrome in tertiary care. Furthermore, this study aims to determine the response rate of the strict low FODMAP diet in non-responders to the DOMINO diet.

CONDITIONS

Official Title

Efficacy of the DOMINO Diet App in IBS

Who Can Participate

Age: 18Years - 70Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Voluntary written informed consent obtained prior to screening
  • Use of highly effective birth control methods or true sexual abstinence during the study risk period
  • Diagnosis of Irritable Bowel Syndrome by Rome IV criteria
  • Age between 18 and 70 years old
Not Eligible

You will not qualify if you...

  • History of major psychiatric disorders, depression, or substance abuse in the last 2 years
  • Any condition that could risk participant safety or study compliance
  • Prior or concurrent treatments that could affect safety or study integrity
  • Female who is pregnant, breastfeeding, or not using effective contraception if of child-bearing potential
  • Participation in other interventional trials with investigational products or devices
  • Predominant symptoms of functional dyspepsia or gastro-oesophageal reflux disease
  • Following a diet that interferes with the study diet as judged by the investigator
  • Previous unsuccessful low FODMAP diet under dietitian guidance

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

UZ Leuven

Leuven, Belgium

Actively Recruiting

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Research Team

J

Jan Tack

CONTACT

K

Karen Routhiaux

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

NON_RANDOMIZED

Model

PARALLEL

Primary Purpose

TREATMENT

Number of Arms

2

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