ClinicalTrials.gg
Not yet recruitingNCT07916493Updated Nov 9, 2026

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

An interventional study of Pilates and Combined Resistance and Aerobic Training in Inflammatory Bowel Disease (Crohn's Disease and Ulcerative Colitis), sponsored by Szeged University. Not yet recruiting. Open to participants aged 18 Years and older. Per ClinicalTrials.gov, last updated 2026-11-09.

Primary conditionColitis, UlcerativeRegistry: Inflammatory Bowel DiseasesReclassifiedWhy we changed it
Registry
Inflammatory Bowel Diseases — the first condition term the registry derived for this study.
ClinicalTrials.gg
Colitis, Ulcerative
Why
  1. The study's listed conditions name Colitis, Ulcerative, a narrower term within Inflammatory Bowel Diseases.
Confidence
High: the new condition is named in the study's own listed conditions. Of 351 hand-checked studies reclassified this way, 68% were exactly right and 84% in the right disease family; the registry's first term was right for 5% (measured 2026-10-21). How we classify →
Wrong?
Tell us the study's main condition →

Sponsored by Szeged University · Not applicable, Interventional, and Supportive care

Updated Nov 9, 2026Primary outcomes revisedNewly registeredGo to Updates ↓
Phase
Not applicable
Study type
Interventional
Enrollment
150
Allocation
Randomized
Ages
18 Years and older
Sex
All
01

Study summary

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.

02

Conditions studied

  • Inflammatory Bowel Disease (Crohn's Disease and Ulcerative Colitis)

Browse trials for

03

In context

Colitis, Ulcerative Reclassified

1,853 studies on the registry are indexed under Colitis, Ulcerative; 472 are open to participants now.

This study's planned enrollment of 150 is above the median of 70 across 1,236 interventional studies indexed under Colitis, Ulcerative.

Browse Colitis, Ulcerative studies →

Lead sponsor

Szeged University is the lead sponsor of 56 studies on the registry; 8 are open to participants now.

Compared within Colitis, Ulcerative, this study's primary condition as ClinicalTrials.gg classifies it; the registry's first condition term is Inflammatory Bowel Diseases. The counts are of registry records indexed under each term, refreshed daily. How we classify →

04

Who can participate

Ages eligible
18 Years and older
Sexes eligible
All
Accepts healthy volunteers
No

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

    • Age >18 years

      • Confirmed diagnosis of IBD
      • Signed

Exclusion criteria

Exclusion Criteria:

    • Presence of comorbidities

      • History of traumatic event
Terms in these criteria, in plain language(1)

Underlined terms in the criteria open these too. Explained by clinicaltrials.gg, not part of the registry record. The study team decides who can take part.

Informed consent

Before you join, the study team explains what taking part involves — its purpose, what happens, the risks and possible benefits — and answers your questions, so you can decide freely. Consent is usually recorded on a form (the informed consent form, ICF) signed by you or, where the law allows, by someone legally authorised to decide for you.

You can keep asking questions during the study, you are told of new information that matters, and you can choose to leave at any time.

05

Study design

Phase
Not applicable
Primary purpose
Supportive care
Allocation
Randomized
Intervention model
Parallel assignment
Masking
None (open label)
Enrollment
150 participants (estimated)

Study arms

  • Active comparator
    Pilates Group

    Other: Pilates

  • Active comparator
    Combined Resistance and Aerobic Training Group

    Other: Combined Resistance and Aerobic Training

  • No intervention
    Control Group

Interventions

  • OtherPilates

    The interventions in this study are distinguished by the use of two different physiotherapist-designed, structured exercise programs delivered through online instructional videos to adults with inflammatory bowel disease (IBD). Both programs will be performed twice weekly for 12 weeks, with each session lasting 20-30 minutes. The Pilates intervention emphasizes controlled movements, breathing techniques, postural correction, stability, mobility, and strengthening of the abdominal, back, and gluteal muscles.

  • OtherCombined Resistance and Aerobic Training

    The interventions in this study are distinguished by the use of two different physiotherapist-designed, structured exercise programs delivered through online instructional videos to adults with inflammatory bowel disease (IBD). Both programs will be performed twice weekly for 12 weeks, with each session lasting 20-30 minutes. The combined resistance and aerobic training intervention includes strengthening exercises targeting all major muscle groups, using body weight and everyday household items, with exercises performed at varying intensities and instructions for manual heart rate monitoring.

06

What researchers measure

Primary outcomes

  1. Change in kinesiophobia level

    Change in kinesiophobia level from baseline to the end of the 12-week intervention, assessed using the Tampa Scale for Kinesiophobia (TSK), a 17-item questionnaire with total scores ranging from 17 to 68, where higher scores indicate a higher level of kinesiophobia (worse outcome). Changes in kinesiophobia will be compared between the Pilates group, the combined resistance and aerobic training group, and the control group.

    Time frame: Baseline and at 12 weeks

07

Study locations

No study locations are listed for this record.

08

Updates

2 registry updates since Sep 25, 2026
Primary outcomes
1 description edited
What changed in the outcomes
  • DescriptionChange in kinesiophobia level: how it is measured was reworded
Nov 9, 2026
Registered
First appeared on the registry
Nov 4, 2026
Show all 2 updates
  1. Nov 9, 2026
    Primary outcomes 1 description edited
    What changed in the outcomes
    • DescriptionChange in kinesiophobia level: how it is measured was reworded
    + 1 other change: verification date
  2. Nov 4, 2026
    First appeared on the registry

From the registry record's own update history. This site started tracking changes on Sep 25, 2026; for anything earlier, see the record history on ClinicalTrials.gov ↗

09

Registry details

Key details

Study ID
NCT07916493
Lead sponsor
Szeged University
Responsible party
Sponsor
First posted
Nov 4, 2026
Start date
Nov 1, 2026 (estimated)
Primary completion
Jan 1, 2027 (estimated)
Completion
Feb 1, 2027 (estimated)
Last update
Nov 9, 2026

Oversight

FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is not yet recruiting, as verified in Nov 2026. You cannot join it, but the record below documents what was studied.

Follow this study

Get an email when the registry record changes — status, dates, results — or when someone posts here.

Sign in to follow

Discussion

Questions and observations about this study, from anyone following it. Not medical advice, and not a channel to the study team — their contact details are on the registry record.

Sign in to join the discussion. Reading takes no account; posting does. You choose a display name, and a pseudonym is the default.

Nothing here yet. If you are running this trial, taking part in it, or weighing whether to, this is the place to say so.

Start the discussion