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Not yet recruiting NCT06981650

Video Education to Improve First Time Colonoscopy Outcomes

No phase Interventional Colonoscopy Education

For patients and families

In plain language

An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.

What is being studied
The protocol lists: video, education.
Who it may be relevant to
Registry conditions: Colonoscopy Education. Basic parameters: 18 years — 75 years · All.
What needs checking
Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
Where it takes place
Center list to be confirmed — check the primary protocol.
Next step
Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
Official title

Video Education to Improve First Time Colonoscopy Outcomes: A Prospective Randomized Control Trial.

Overview

The investigators compare video education plus standard education versus standard education for bowel preparation before a colonoscopy. The primary outcome will be the quality of bowel preparation.

Detailed description

The investigators compare video education plus standard education versus standard education for bowel preparation before a colonoscopy and include a number of languages including English, Spanish, Russian, Haitian Creole, and Urdu. The educational content also includes psychological content based upon the Theory of Planned Behavior. The primary outcome will be the quality of bowel preparation, as measured by the Boston Bowel Preparation Scale (BBPS) score,

Interventions

  • Behavioral video
    use of a video
  • Behavioral education
    standard talk and paper handout

Primary outcome measures

  • Boston Bowel Preparation Scale (continuous) [Time frame: Perioperative/Periprocedural]
Secondary outcome measures (9)
  • Boston Bowel Preparation Scale (categorical) [Time frame: Perioperative/Periprocedural]
  • Polyp detection rate proportion [Time frame: Perioperative/Periprocedural]
  • Adenoma detection rate proportion [Time frame: Perioperative/Periprocedural]
  • Cecal intubation rate proportion [Time frame: Perioperative/Periprocedural]
  • Withdrawal time [Time frame: Perioperative/Periprocedural]
  • Adherence to bowel preparation instructions [Time frame: Perioperative/Periprocedural]
  • Amsterdam Preoperative Anxiety and Information Scale [Time frame: baseline]
  • Overall experience with the bowel preparation process [Time frame: Perioperative/Periprocedural]
  • Desire to undergo future colonoscopies if indicated [Time frame: Perioperative/Periprocedural]

Eligibility criteria

Inclusion Criteria: all outpatients aged 18 to 75 years scheduled for their first screening colonoscopy

\-

Exclusion Criteria: ● Contraindications for colonoscopy

  • History of bowel surgery, particularly colorectal surgery
  • Severe comorbid conditions (e.g., impaired hepatic, renal or bone marrow function, congestive heart failure, recent coronary artery disease)
  • Chronic constipation (typically <3 bowel movements per week with hard stools, a feeling of incomplete evacuation, or abdominal discomfort) requiring the use of laxatives
  • Pregnancy or lactation
  • Prisoners
  • Diagnosis of inflammatory bowel disease
  • Inability to use video presentation devices (e.g., blindness)
  • Active cancers.

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: No

Study design

Allocation
Randomized
Model
Parallel assignment
Masking
Open label
Primary purpose
Screening

Study locations

Center list to be confirmed — check the primary protocol.

Publications

  • Mahmood S, Farooqui SM, Madhoun MF. Predictors of inadequate bowel preparation for colonoscopy: a systematic review and meta-analysis. Eur J Gastroenterol Hepatol. 2018 Aug;30(8):819-826. doi: 10.1097/MEG.0000000000001175. PMID 29847488

Identifiers

NCT: NCT06981650 · MED2024-555

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗