Eligibility Module

Eligibility Module

The Eligibility Module contains detailed information about who can participate in the clinical trial. This includes eligibility criteria, age restrictions, gender requirements, healthy volunteer status, and study population descriptions, helping researchers understand who is eligible to participate in the study.

Eligibility Module path is as follows:

Study -> Protocol Section -> Eligibility Module

Eligibility Module


Ignite Creation Date: 2025-12-24 @ 10:07 PM
Ignite Modification Date: 2025-12-24 @ 10:07 PM
NCT ID: NCT06427135
Eligibility Criteria: Inclusion Criteria: * Commitment to comply with the study procedures and cooperate in the implementation of the full study * Age ≥ 18 years old, gender is not limited * Muscle strength examination of all four limbs is greater than or equal to grade 3 * Patients with a diagnosis of CD or UC in combination with clinical presentation, laboratory examination, endoscopy, imaging and histopathologic examination, with a disease course in mild to moderate activity or remission * Presence of low or high BMI, malnutrition, muscular dystrophy, and anxiety * Voluntarily sign a written informed consent Exclusion Criteria: * Absolute contraindications to exercise: acute stages of various diseases (e.g. cerebral hemorrhage, acute stage of myocardial infarction), severe complications, severe cardiopulmonary dysfunction, severe gastrointestinal problems (e.g. gastric perforation, intestinal obstruction), severe locomotor system disorders (e.g. severe bone fracture), as well as other diseases that are not under effective control * Relative contraindications to exercise: severe hypertension, severe diabetes, chronic pain, cardiac arrhythmia, etc * Persons with unstable vital signs * Presence of cognitive, communication disorders * Patients who have recently undergone gastrointestinal surgery (\<1 month) or who have not fully healed * Short bowel syndrome * Presence of extra-intestinal manifestations and complications that interfere with therapy, such as retinopathy, deep vein thrombosis, etc * Pregnant or lactating women * Active tuberculosis; if subjects are suspected of having active tuberculosis, chest X-ray, sputum and exclusion by clinical signs and symptoms are required * Other potential subjects who are not suitable for participation in this study
Healthy Volunteers: False
Sex: ALL
Minimum Age: 18 Years
Maximum Age: 60 Years
Study: NCT06427135
Study Brief:
Protocol Section: NCT06427135