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IBS - Irritable Bowel Syndrome clinical trials

View clinical trials related to IBS - Irritable Bowel Syndrome.

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NCT ID: NCT05118243 Active, not recruiting - Clinical trials for IBS - Irritable Bowel Syndrome

Innovative Tools to Produce Legume-based Foods for Increased Consumer Acceptance

LeguComf
Start date: September 6, 2021
Phase: N/A
Study type: Interventional

The aim of this study is to investigate the effects of enzymatic treatment to reduce GOS (galactooligosaccharides) in legume-based crackers in IBS (irritable bowel syndrome) persons. The crackers are pea-based: the control crackers contain high amounts of GOS, while the enzymatically treated crackers contain a minimal amount of GOS. The participants will eat each type of cracker for three days (daily dose of 12 crackers) and report their gut symptoms (e.g. flatulence, stomach pain, bloating) by using a mobile app. There is a washout period of four days between the different crackers. In addition, the participants will keep food records on the cracker eating days as well as collect five fecal samples during the study. The participants will also report their physical activity and the number of defecations on each day. The study is carried out in a double-blinded crossover setting.

NCT ID: NCT04723056 Active, not recruiting - Clinical trials for IBS - Irritable Bowel Syndrome

Zemedy Application for Irritable Bowel Syndrome

Start date: October 15, 2021
Phase: N/A
Study type: Interventional

The purpose of the study is investigate the effectiveness of Zemedy, a mobile application that enables the digital delivery of a CBT program to people with IBS.

NCT ID: NCT03432078 Active, not recruiting - Clinical trials for IBS - Irritable Bowel Syndrome

Individual vs. Group Hypnotherapy in Patients With Irritable Bowel Syndrome

Start date: August 15, 2011
Phase: N/A
Study type: Interventional

Patients' fulfilling Rome III criteria for IBS with symptoms refractory to standard treatment who are referred to a specialist unit for hypnotherapy are consecutively included in the study. The patients are randomized to either individual or group treatment given by a nurse trained in hypnotherapy. The treatment consists of eight sessions of gut directed hypno therapy during twelve weeks. Effects are measured by validated questionnaires at baseline and at various time points during the treatment period as well as after the completion of the treatment.