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Clinical Trials in China / NCT06804733
Recruiting Not applicable

Efficacy of Individualized Aerobic Exercise Training in Patients With Inflammatory Bowel Disease

NCT06804733 · tracked via the Priya Life Science China tracker
Sponsor
Ningbo Medical Center Lihuili Hospital
Phase
Not applicable
Started
2025-05-01
Last updated
2025-12-16

Condition(s) studied

Inflammatory Bowel Disease (IBD)

Investigational drug(s) / intervention(s)

12-week individualized aerobic exercise training12-week control intervention followed by 12-week aerobic exercise training

12-week individualized aerobic exercise training: After enrollment, subjects directly participate in a 12-week aerobic exercise training program. The training plan provides individualized progressive aerobic training based on their baseline physical activity level measured by International Physical Activity Questionnaire (IPAQ), with the exercise intensity being increased every four weeks.

12-week control intervention followed by 12-week aerobic exercise training: After enrollment, subjects first undergo a 12-week control intervention (i.e., routine treatment) and then participate in a 12-week aerobic exercise training program. The training plan provides individualized progressive aerobic training based on their baseline physical activity level IPAQ, with the exercise intensity being increased every four weeks.

Study summary

The goal of this clinical trial is to learn if a 12-week individualized aerobic training program helps manage inactive or mildly active inflammatory bowel disease (IBD) including Crohn's disease (CD) and ulcerative colitis (UC) in adult patients aged 18-65 years. It will also assess participant compliance and the safety of the training program. The main questions it aims to answer are:

1. Does this aerobic training program improve the cardiopulmonary function of participants?
2. Does this aerobic training program help control disease activity?
3. Does this aerobic training program improve participants' quality of life?

Researchers will divide participants into two groups. One group will participate in the training program directly. The other group will first undergo a 12-week control intervention (i.e., standard treatment) before proceeding to the training program.

Participants will:

1. Take part in the individualized aerobic training program according to their baseline physical activity level for 12 weeks.
2. Visit the clinic once every 4 weeks for check-ups and tests.
3. Keep a diary of symptoms.

Eligibility

Sex
ALL
Min age
18 Years
Max age
65 Years
Healthy volunteers
No
Inclusion Criteria: * Diagnosed with CD or UC for more than 3 months. * Disease activity in remission or mildly active (CD: CDAI \< 220; UC: pMS \< 5). * Baseline physical activity intensity is low, measured by the IPAQ Chinese version short form, and without a habit of "regular exercise". * Agree to participate in the study and accept a 12-week individualized aerobic exercise training program. Exclusion Criteria: * Pregnant or breastfeeding, or planning to become pregnant within the next 3 months. * Presence of physical movement disorders or other chronic diseases that limit physical activity. * Having an ileostomy. * History of anal or intestinal surgery within the past 3 months.

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
the Affiliated Lihuili Hospital of Ningbo University Ningbo Zhejiang Recruiting

More Ningbo Medical Center Lihuili Hospital trials in China

Other trials for the same condition

Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT06804733 on ClinicalTrials.gov ↗ ← All trials in China