Individualized, non-drug prep to improve bowel cleaning for colonoscopy
Official title: Effect of an Individualized Non-pharmacological Intervention Based on a Predictive Model for Inadequate Bowel Preparation on Bowel Preparation Quality: a Three-arm, Prospective, Randomized Controlled Study
Run by General Hospital of Shenyang Military Region · NCT07684716 · Data updated 2026-11-12
This trial tests whether an individualized non-pharmacological plan—plus tailored information framing—can improve bowel preparation quality for adults undergoing colonoscopy.
Quick facts
| Study type | Interventional |
|---|---|
| Ages | 18 Years and up |
| Sex | All |
| Enrollment | 339 (estimated) |
| Sponsor | General Hospital of Shenyang Military Region Academic / other |
| Locations | 1 site (Shenyang, Liaoning) |
| Status | Recruiting |
| Started | June 8, 2026 |
| Main results expected | August 30, 2026 |
| Study ends | September 30, 2026 |
| Registry record updated | July 6, 2026 |
| Trial ID | NCT07684716 on ClinicalTrials.gov |
Is this trial a fit for you?
✓Likely a good fit
Adults 18 years or older scheduled for outpatient colonoscopy who can provide informed consent.
✕Probably not a fit
Patients who are not adherent to non-pharmacological recommendations or who have conditions that necessitate pharmacological regimens may see no benefit.
A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.
What this trial studies
Adults scheduled for colonoscopy are randomized to three groups to see if an information-framing and tailored non-pharmacological regimen improves bowel cleanliness compared with standard prep. The study uses a risk score to tailor bowel prep intensity and adds illustrated education; the information framing varies by risk to emphasize harms or benefits of adherence. Endoscopists rate bowel cleanliness with the Boston Bowel Preparation Scale, while participants report adherence and motivation. Outcomes include prep quality, willingness for repeat procedures, and adverse events, with blinded assessment of results.
Why it matters
Potential benefit: If successful, patients may experience better bowel cleanliness, shorter procedures, and potentially fewer complications or repeat procedures.
How similar studies have gone: Previous work suggests education and non-pharmacological strategies can improve adherence, but this specific framed, individualized approach is novel.
Who can join: the full rules
Show full inclusion / exclusion criteria
Inclusion Criteria: * age ≥ 18 years; * outpatient scheduled for colonoscopy using oral laxatives for bowel preparation; * able to understand the study and provide written informed consent. Exclusion Criteria: * undergoing emergency colonoscopy; * suspected intestinal obstruction, stricture, or perforation; * severe cardiac, cerebral, hepatic, or renal disease; * severe psychiatric disorder; * impaired consciousness or communication difficulties; * pregnancy or lactation; * previous enrollment in this study.
Where it's running
-
General Hospital of Northern Theater Command
Shenyang, Liaoning, China Recruiting
Study contacts
- Study coordinator: Xingshun Qi
- Email: xingshunqi@126.com
- Phone: +8618909881019
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How to take part
- Review the eligibility criteria above with your treating physician.
- Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
- Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.