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NCT07916493Not yet recruiting

Effects of Different Physical Activity Strategies on Disease Activity of IBD Patients

Source: ClinicalTrials.gov · Last updated 4 Nov 2026

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Brief summary (registry, in English)

The goal of this randomized controlled trial is to evaluate the effects of two different exercise programs, Pilates and combined resistance and aerobic training, on physical activity, kinesiophobia, quality of life, and disease-related outcomes in adults with inflammatory bowel disease (IBD), including Crohn's disease and ulcerative colitis. The main questions it aims to answer are: * Do the two exercise programs improve physical activity levels, reduce kinesiophobia, and improve quality of life in adults with IBD? * Are there differences between Pilates and combined resistance and aerobic training in their effects on participants' health status and disease-related outcomes? Researchers will compare participants assigned to the Pilates group and the combined resistance and aerobic training group with participants in the control group to evaluate the effects of the exercise programs. Participants will be randomly allocated to one of three groups: a Pilates group, a combined resistance and aerobic training group, or a control group. Participants in the exercise groups will follow their assigned exercise program using online instructional videos twice a week for 12 weeks, with each session lasting 20-30 minutes. They will record completed exercise sessions in an exercise diary. All participants will complete questionnaires before and after the intervention to assess physical activity, kinesiophobia, quality of life, depressive symptoms, knowledge of physical activity, and attitudes towards physiotherapists. Relevant demographic and clinical data will also be collected from medical records.

Status (registry)
Not yet recruiting
Study type
Interventional
Enrollment
150 (estimated)
First submitted
29 Oct 2026
Start date
1 Nov 2026
Primary completion date
1 Jan 2027
Lead sponsor
Szeged University
NCT number
NCT07916493

What you commit to

  • Study type: Interventional
  • Planned participants: 150
  • From 1 Nov 2026 to the primary completion date, 1 Jan 2027
  • No sites listed in no country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study design.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Other illness

  • • Presence of comorbidities
    • History of traumatic event

Who the study is looking for

  • • Age >18 years
    • Confirmed diagnosis of IBD
    • Signed informed consent

Age in the registry: 18 years to - · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

This page is information, not medical advice. Discuss any trial with your doctor.