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 · Status: NOT_YET_RECRUITING · Phase: NA · Type: INTERVENTIONAL · Enrollment: 600

Last updated 2026-06-16

No results posted yet for this 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.

Conditions

  • Inflammatory Bowel Diseases

Interventions

BEHAVIORAL

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.

BEHAVIORAL

standard bowel preparation education

standard bowel preparation education

Sponsors & Collaborators

  • Xijing Hospital of Digestive Diseases

    collaborator OTHER
  • Peking Union Medical College Hospital

    collaborator OTHER
  • Shengjing Hospital

    collaborator OTHER
  • RenJi Hospital

    collaborator OTHER
  • Changhai Hospital

    collaborator OTHER
  • First Affiliated Hospital of Xinjiang Medical University

    collaborator OTHER
  • Affiliated Hospital of Qinghai University

    collaborator OTHER
  • Second Affiliated Hospital of Xi'an Jiaotong University

    collaborator OTHER
  • Air Force 986 Hospital

    collaborator OTHER
  • Shanxi Yuncheng Central Hospital

    collaborator UNKNOWN
  • Ruijin Hospital

    collaborator OTHER
  • Changzhi Medical College

    collaborator OTHER
  • Linfen Central Hospital

    collaborator OTHER
  • Jie Liang

    lead OTHER

Study Design

Allocation
RANDOMIZED
Purpose
SUPPORTIVE_CARE
Masking
SINGLE
Model
PARALLEL

Eligibility

Min Age
18 Years
Max Age
75 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2026-06-01
Primary Completion
2027-06-01
Completion
2027-07-01

Countries

  • China

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT07582731 on ClinicalTrials.gov