The goal of this clinical trial is to learn if abdominally targeted exercises can assist to manage disease activity in Crohn disease (CD) patients. The main questions it aims to answer are: Does abdominally targeted exercises can improve the quality of life of CD patients. Does abdominally targeted exercises positively influence clinical and biological responses in CD patients. Researchers will compare performing sets of special physical exercises designed for CD patients, compared to a control set of exercises ("generic" physical activity) to see if exercises designed for CD can result in an improved quality of life, in CD patients suffering from mild to moderate disease activity. Participants will: * Perform physical exercises designed for CD or control set of exercises every day for 8 weeks. * Visit the clinic once every 4 weeks for doctor visit, blood and stool test and filling out questionnaires.
Age range
18 Years – 60 Years
Sex
ALL
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Generated to help you prepare — always confirm anything about your own eligibility and care with the study team and your doctor.
The trial coordinator is the person who runs the study day to day. These cover the practical side — logistics, costs, and what taking part would actually mean for your life. The study team confirms whether you meet the criteria; these are questions to ask, not a sign you qualify.
A starting point for the conversation — always confirm anything about your own eligibility, costs, and care with the study team and your doctor.
Clinical response rate
Timeframe: From enrollment to the end of treatment at 8 weeks
Clinical remission rate
Timeframe: From enrollment to the end of treatment at 8 weeks
Biomarker remission rate
Timeframe: From enrollment to the end of treatment at 8 weeks
Biomarker remission rate
Timeframe: From enrollment to the end of treatment at 8 weeks
Change from Baseline in mean values of PROMIS-29 scores
Timeframe: From enrollment to the end of treatment at 8 weeks
Change from Baseline in mean values of IBDQ
Timeframe: From enrollment to the end of treatment at 8 weeks