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Clinical Trials in China / NCT07582731
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A Multi-Center Randomized Controlled Trial on the Impact of Disease Subtype-Based Active Video Education on Bowel Preparation Quality in Patients With Inflammatory Bowel Disease

NCT07582731 · tracked via the Priya Life Science China tracker
Sponsor
Jie Liang
Phase
Not applicable
Started
2026-06-01
Last updated
2026-06-16

Condition(s) studied

Inflammatory Bowel Diseases

Investigational drug(s) / intervention(s)

Disease Subtype-Based Active Video Educationstandard bowel preparation education

Disease Subtype-Based Active Video Education: A structured, subtype-specific educational video program tailored for patients with inflammatory bowel disease (IBD). The videos are customized based on IBD subtype (ulcerative colitis/Crohn's disease), disease activity (active/remission), and Crohn's disease behavior (stricturing/fistulizing). It covers key topics including dietary restrictions, laxative intake instructions, symptom management, and practical problem-solving strategies to improve understanding and adherence to bowel preparation protocols. The video is delivered via WeChat link.

standard bowel preparation education: standard bowel preparation education

Study summary

This multi-center, prospective, randomized controlled trial evaluates whether disease subtype-based active video education improves bowel preparation quality in patients with inflammatory bowel disease (IBD) undergoing colonoscopy. A total of 600 IBD patients from 13 centers will be randomized 1:1 to standard education plus subtype-specific video education (intervention group) or standard education alone (control group). The primary outcome is the Boston Bowel Preparation Scale (BBPS) score.

Eligibility

Sex
ALL
Min age
18 Years
Max age
75 Years
Healthy volunteers
No
Inclusion Criteria: 1. Age between 18 and 75 years, inclusive. 2. Confirmed diagnosis of Ulcerative Colitis (UC) or Crohn's disease (CD) according to standard clinical guidelines. 3. Scheduled for elective colonoscopy for IBD monitoring or disease activity assessment. 4. Able to understand written and verbal instructions and to use a smartphone to view video education materials. 5. Voluntary participation with written informed consent. Exclusion Criteria: 1. Absolute contraindications to colonoscopy, including acute gastrointestinal perforation, fulminant colitis, toxic megacolon, or hemodynamic instability. 2. History of total or subtotal colectomy. 3. Acute or chronic intestinal obstruction. 4. Severe cardiac, pulmonary, hepatic, or renal insufficiency (eGFR \<30 mL/min/1.73m², NYHA class III/IV). 5. Severe psychiatric or cognitive impairment that prevents understanding of the study requirements. 6. Inability or unwillingness to provide written informed consent. 7. Pregnant or breastfeeding women.

Primary outcome measure(s)

Trial sites (12)

FacilityCityRegionStatus
Peking Union Medical College Hospital Beijing BeijingBeijing
Shengjing Hospital of China Medical University Shenyang Liaoning
Affiliated Hospital of Qinghai University Xining Qinghai
The Second Affiliated Hospital of Xi'an Jiaotong University Xi'an Shaanxi
Air Force 986 Hospital Xi'an Shaanxi
Ruijin Hospital, Shanghai Jiao Tong University School of Medicine Shanghai Shanghai Municipality
Renji Hospital, Shanghai Jiao Tong University School of Medicine Shanghai Shanghai Municipality
Changhai Hospital, Naval Medical University Shanghai Shanghai Municipality
Heping Hospital affiliated to Changzhi Medical College Changzhi Shanxi
Linfen Central Hospital Linfen Shanxi
Yuncheng Central Hospital Yuncheng Shanxi
The First Affiliated Hospital of Xinjiang Medical University Ürümqi Xinjiang

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 NCT07582731 on ClinicalTrials.gov ↗ ← All trials in China